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Scleroderma Patient-centered Intervention Network (SPIN) Hand Program Feasibility Study

Feasibility Trial of an Internet-based Exercise Program to Improve Hand Function in Patients With Scleroderma: A Scleroderma Patient-centered Intervention Network (SPIN) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03092024
Acronym
SPIN-HAND-F
Enrollment
40
Registered
2017-03-27
Start date
2017-06-01
Completion date
2017-10-17
Last updated
2021-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scleroderma, Systemic Sclerosis

Keywords

Systemic Sclerosis, Scleroderma, Hand, Intervention, Exercise

Brief summary

The Scleroderma Patient-centered Intervention Network (SPIN) is an organization established by researchers, health care providers, and people living with scleroderma from Canada, the USA, and Europe. The objectives of SPIN are (1) to assemble a large cohort of scleroderma patients to complete outcome assessments regularly in order to learn more about important problems faced by people living with scleroderma and (2) to develop and test a series of internet-based interventions to help patients manage aspects of scleroderma, including hand limitations. In the SPIN-HAND feasibility trial, SPIN Cohort participants with at least mild hand function limitations and an indicated interest in using an online hand exercise program will be randomized to be offered the SPIN hand exercise program or to usual care only. The core SPIN hand exercise program consists of 4 modules that address specific aspects of hand function, including Thumb Flexibility and Strength; Finger Bending; Finger Extension; and Wrist Flexibility and Strength. The program also integrates tools to support key components of successful self-management programs, including goal-setting. The aim of the SPIN-HAND feasibility study is to collect data to assess the feasibility of the steps that need to take place as part of the main trial; required resources; and scientific aspects (e.g., withdrawal rate, outcomes measures). Data will be used to determine whether it is feasible to carry out the main study or whether changes need to be made before conducting a full-scale RCT of the SPIN-HAND program.

Detailed description

The SPIN Cohort currently currently includes over 1700 patients from 36 sites in Canada, the USA, France, and the United Kingdom. It is anticipated that the Cohort will grow to approximately 2,000 patient by the end of 2017. SPIN Cohort patients complete outcome measures via the internet upon enrolment and subsequently every 3 months. SPIN utilizes the cohort multiple RCT (cmRCT) design as a framework for conducting trials of interventions. SPIN Cohort patients consent to allow personal data to be used for observational research, to assess intervention trial eligibility and, if eligible, be randomized. Patients also consent that if eligible and randomized to usual care, the patient's data can be used to evaluate intervention effectiveness without the patient being notified that the patient has been randomized to the usual care group and not offered the intervention. Thus, in SPIN trials, trial status is masked for patients in the control arm, who are not aware that they are in the trial, but not patients in the intervention arm. The investigative team does not interact with patients for care provision or outcome assessment, which are done automatically via the internet. The SPIN-HAND feasibility study is embedded in the SPIN Cohort and will evaluate the feasibility of conducting full-scale RCT on the SPIN-HAND exercise program. Investigators will randomize 36-40 SPIN Cohort patients with at least mild hand function limitations and an indicated interest in using an online hand exercise program to be offered the hand exercise program or usual care only. Randomization will occur at the time of patients' regular SPIN Cohort assessments. Eligible patients, based on questionnaire responses, will be randomized automatically using simple 1:1 randomization, using a feature in the SPIN Cohort platform, which provides immediate randomization and complete allocation sequence concealment. Feasibility outcomes include patient eligibility and recruitment and numbers and percentages of patients who do not respond to follow-up measures. Use of the internet intervention will be described by presenting the frequency of logins and time spent on the SPIN-HAND program. Analysis of outcome measures will include the completeness of data and presence of floor or ceiling effects. Descriptive statistics will be used to provide means and standard deviations for the measures. Qualitative information and information related to management and usability of the SPIN-HAND program will inform any necessary changes to the intervention or trial procedures.

Interventions

The internet-based SPIN-HAND program consists of 4 modules (1) Thumb Flexibility and Strength (3 exercises); (2) Finger Bending (3 exercises); (3) Finger Extension (3 exercises); and (4) Wrist Flexibility and Strength (2 exercises). The program includes sections on developing a personalized program, goal-setting strategies and examples, progress tracking, sharing goals and progress with friends and family, and patient stories of experiences with hand disability and hand exercises. Instructional videos demonstrate and explain how to perform each exercise properly with pictures to illustrate common mistakes. Separate versions of each exercise are available for patients with mild/moderate and more severe hand involvement.

Sponsors

Hôpital Cochin
CollaboratorOTHER
Lady Davis Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* SPIN Cohort patients must have a systemic sclerosis (SSc) diagnosis based on 2013 American College of Rheumatology/European League Against Rheumatism criteria confirmed by a SPIN physician, be ≥18 years old, be able to give informed consent, and be fluent in English or French. * For the feasibility trial, eligible patients will be able to use the online intervention in English, have at least mild hand function limitations (Cochin Hand Function Scale ≥ 3) and have indicated high interest in using an online hand exercise intervention (≥7 on 0-10 scale).

Exclusion criteria

* Patients not able to access or respond to questionnaires via the internet are excluded.

Design outcomes

Primary

MeasureTime frameDescription
Count of Participants Who Reported Technological Problems During Post-trial Patient Interviews3 monthsMeasure: count of technological problems reported SPIN personnel reported no issues with the technological performance of the online SPIN-HAND program. As part of the user feedback interviews, participants of the SPIN-HAND program were asked whether they experienced technological difficulties during the intervention. Here, we report the number of intervention-arm participants who reported technological issues, during these post-trial interviews. In cases of technological difficulty experienced by participants, technological assistance was provided by the SPIN team, and the issues were resolved.
Participant Grade on Usability of the SPIN-HAND Program Based on Post-trial Patient Interviews3 monthsAt 3-months post-randomization, qualitative semi-structured interviews were conducted with participants in the intervention arm to assess user acceptability and satisfaction. The interview, consisting of 29 questions, was guided by items of the Patient Education Materials Assessment Tool for Audiovisual Materials and addressed topics related to usability, understandability, organization, and clarity. During these interviews, participants were asked to give the SPIN-HAND program a grade ranging from 0-10, 0 being the worst and 10 being the best possible score. In this table, we report the overall mean grade reported by the intervention arm participants who agreed to be interviewed post-trial.
Intervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online Features3 monthsUsage of the online SPIN-HAND program was measured based on usage log data, notably the number of participants who logged into the program once, twice or more than two times. Program usage was also measured based on the number of participants who accessed different parts of the online SPIN-HAND program including: the introduction videos, the website tour, the page explaining the level of hand involvement to identify the exercises most relevant to them, the four available modules of the online SPIN-HAND program, as well as the goal-setting feature.
Usage Log Data: Completeness of the Automatic Usage Log Data Values Collected3 monthsHere we report our success in collecting participant usage log data. This is reported as the percentage of the usage log data that was successfully collected.
Usage Log Data: Linking of Data From the SPIN Cohort and SPIN-HAND Platforms.3 monthsWe report our percentage success in linking data coming from the SPIN Cohort and SPIN-HAND platforms.
Eligibility: Number of Patients in the SPIN Cohort Who Meet the Cut-off Thresholds for EligibilitybaselineMeasure: count of eligible patients
Enrolment: Percentage of Patients Who Consent to ParticipationBaselineMeasure: count of consenting patients Participants randomized to be offered the intervention received an automated email invitation including a link to the SPIN-HAND Program site and the consent form for the intervention. Participants who were randomized to care as usual were not notified that they had not been offered the intervention and completed their regular SPIN Cohort assessments. Thus, participants who were offered the intervention were not blind to their status, whereas participants assigned to usual care were blind to their participation in the trial and to their assignment to usual care.

Secondary

MeasureTime frameDescription
EuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelBaseline, 3 monthsThe EuroQol Group 5 Dimension 5 Level (EQ-5D-5L) is standardized questionnaire measuring 5 dimensions related to health related quality of life, mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. For each dimension, items are rated from 1 (no problems) to 5 (extreme problems). Here we report the number of intervention arm and control arm participants who gave scores ranging 1-5 for the different dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression), at baseline and at 3-months post randomization.
EuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated HealthBaseline, 3 monthsAs part of the EQ-5D-5L questionnaire, a Visual Analogue Scale (VAS) records the patient's self-rated health on a scale from 0-100 where the endpoints are labelled 'the best health you can imagine' (100) and 'the worst health you can imagine' (0). Here we report the mean (and standard deviations) self-reported patient health VAS scores of intervention arm participants and control arm participants (i.e. usual care), at baseline and at 3-months post-randomization.
Patient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0Baseline, 3 monthsMeasures 8 domains of health status with 4 items for each of 7 domains (physical function, anxiety, depression, fatigue, sleep disturbance, social roles and activities, pain interference) plus a single item for pain intensity. Items are scored on a 5-point scale (range 1-5), with different response options for different domains, and the single pain intensity item is measured on an 11-point rating scale. Higher scores represent more of the domain being measured; that is, better physical function and ability to participate in social roles and activities, but higher levels of anxiety, depression, fatigue, sleep disturbance, pain interference, and pain intensity. Total raw scores are obtained by summing item scores for each domain, which are converted into T-scores standardized from the general US population (mean=50, SD=10). Here, we report the pre- and post-intervention total scores for PROMIS-29 domains.
The Cochin Hand Function Scale (CHFS)Baseline, 3 monthsThe Cochin Hand Function Scale (CHFS) measures functional ability of the hand among patients with rheumatic diseases. The 18-item CHFS measures ability to perform daily hand-related activities (e.g., kitchen, dressing oneself, hygiene, writing/typing). Items are scored on a 0-5 Likert scale (0=without difficulty; 5=impossible). Higher scores indicate less functionality. The total score is obtained by adding the scores of all items (range 0-90).

Countries

Canada

Participant flow

Recruitment details

Assessment of trial eligibility occurred during participants' regular online SPIN Cohort assessments. Enrollment in the feasibility trial started on June 1, 2017 and was completed on June 18, 2017 when 40 eligible SPIN Cohort participants were randomized. Of these, 24 (60%) were allocated to the SPIN-HAND arm, and 16 (40%) to the usual care arm.

Participants by arm

ArmCount
SPIN-HAND Program
SPIN-HAND program: The internet-based SPIN-HAND program consists of 4 modules (1) Thumb Flexibility and Strength (3 exercises); (2) Finger Bending (3 exercises); (3) Finger Extension (3 exercises); and (4) Wrist Flexibility and Strength (2 exercises). The program includes sections on developing a personalized program, goal-setting strategies and examples, progress tracking, sharing goals and progress with friends and family, and patient stories of experiences with hand disability and hand exercises. Instructional videos demonstrate and explain how to perform each exercise properly with pictures to illustrate common mistakes. Separate versions of each exercise are available for patients with mild/moderate and more severe hand involvement.
24
Not Offered the SPIN-HAND Program
Treatment as usual
16
Total40

Baseline characteristics

CharacteristicTotalSPIN-HAND ProgramNot Offered the SPIN-HAND Program
Age, Continuous57.8 years
STANDARD_DEVIATION 14.7
57.1 years
STANDARD_DEVIATION 13.5
58.7 years
STANDARD_DEVIATION 16.8
Country
Canada
12 Participants8 Participants4 Participants
Country
United Kingdom
12 Participants7 Participants5 Participants
Country
United States
16 Participants9 Participants7 Participants
Diffuse disease subtype19 Participants11 Participants8 Participants
Education15.1 years
STANDARD_DEVIATION 3.1
15.0 years
STANDARD_DEVIATION 3.2
15.2 years
STANDARD_DEVIATION 3.1
Large joint contractures8 Participants4 Participants4 Participants
Married or living as married27 Participants17 Participants10 Participants
Modified Rodnan Skin Score12.4 scores on a scale
STANDARD_DEVIATION 11.2
9.7 scores on a scale
STANDARD_DEVIATION 10.8
17.4 scores on a scale
STANDARD_DEVIATION 10.8
Race/Ethnicity, Customized
Black
3 Participants1 Participants2 Participants
Race/Ethnicity, Customized
Other
3 Participants1 Participants2 Participants
Race/Ethnicity, Customized
White
34 Participants22 Participants12 Participants
Sex: Female, Male
Female
36 Participants21 Participants15 Participants
Sex: Female, Male
Male
4 Participants3 Participants1 Participants
Small joints contractures13 Participants6 Participants7 Participants
Tendon friction rubs12 Participants8 Participants4 Participants
Time since diagnosis10.1 years
STANDARD_DEVIATION 7
10.0 years
STANDARD_DEVIATION 6.2
10.1 years
STANDARD_DEVIATION 8.3
Time since onset first non-Raynaud's symptom or sign11.7 years
STANDARD_DEVIATION 7.9
11.8 years
STANDARD_DEVIATION 7
11.6 years
STANDARD_DEVIATION 9.5
Time since onset Raynaud's15.0 years
STANDARD_DEVIATION 12
14.6 years
STANDARD_DEVIATION 11.2
15.7 years
STANDARD_DEVIATION 13.6

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 240 / 16
other
Total, other adverse events
0 / 240 / 16
serious
Total, serious adverse events
0 / 240 / 16

Outcome results

Primary

Count of Participants Who Reported Technological Problems During Post-trial Patient Interviews

Measure: count of technological problems reported SPIN personnel reported no issues with the technological performance of the online SPIN-HAND program. As part of the user feedback interviews, participants of the SPIN-HAND program were asked whether they experienced technological difficulties during the intervention. Here, we report the number of intervention-arm participants who reported technological issues, during these post-trial interviews. In cases of technological difficulty experienced by participants, technological assistance was provided by the SPIN team, and the issues were resolved.

Time frame: 3 months

Population: 6 of the 15 intervention arm participants agreed to be interviewed post-trial. Participants randomized to usual care were not interviewed.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
SPIN-HAND ProgramCount of Participants Who Reported Technological Problems During Post-trial Patient InterviewsParticipants who reported no technology issues4 Participants
SPIN-HAND ProgramCount of Participants Who Reported Technological Problems During Post-trial Patient InterviewsParticipants who reported internet connectivity issues1 Participants
SPIN-HAND ProgramCount of Participants Who Reported Technological Problems During Post-trial Patient InterviewsParticipants who reported login issue (resolved by SPIN team)1 Participants
Not Offered the SPIN-HAND ProgramCount of Participants Who Reported Technological Problems During Post-trial Patient InterviewsParticipants who reported no technology issues0 Participants
Primary

Eligibility: Number of Patients in the SPIN Cohort Who Meet the Cut-off Thresholds for Eligibility

Measure: count of eligible patients

Time frame: baseline

Population: Enrollment in the feasibility trial started on June 1, 2017 and was completed on June 18, 2017 when 40 eligible SPIN Cohort participants were randomized. Of these, 24 (60%) were allocated to the SPIN-HAND arm, and 16 (40%) to the usual care arm.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
SPIN-HAND ProgramEligibility: Number of Patients in the SPIN Cohort Who Meet the Cut-off Thresholds for Eligibility24 Participants
Not Offered the SPIN-HAND ProgramEligibility: Number of Patients in the SPIN Cohort Who Meet the Cut-off Thresholds for Eligibility16 Participants
Primary

Enrolment: Percentage of Patients Who Consent to Participation

Measure: count of consenting patients Participants randomized to be offered the intervention received an automated email invitation including a link to the SPIN-HAND Program site and the consent form for the intervention. Participants who were randomized to care as usual were not notified that they had not been offered the intervention and completed their regular SPIN Cohort assessments. Thus, participants who were offered the intervention were not blind to their status, whereas participants assigned to usual care were blind to their participation in the trial and to their assignment to usual care.

Time frame: Baseline

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
SPIN-HAND ProgramEnrolment: Percentage of Patients Who Consent to Participation15 Participants
Not Offered the SPIN-HAND ProgramEnrolment: Percentage of Patients Who Consent to Participation0 Participants
Primary

Intervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online Features

Usage of the online SPIN-HAND program was measured based on usage log data, notably the number of participants who logged into the program once, twice or more than two times. Program usage was also measured based on the number of participants who accessed different parts of the online SPIN-HAND program including: the introduction videos, the website tour, the page explaining the level of hand involvement to identify the exercises most relevant to them, the four available modules of the online SPIN-HAND program, as well as the goal-setting feature.

Time frame: 3 months

Population: None of the participants randomized to usual care logged into the SPIN-HAND program.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesLogged in 1 time7 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesLogged in 2 times3 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesLogged in more than 2 times5 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who watched introduction videos11 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who used the website tour6 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who accessed page to identify relevant exercises10 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who did not access any module6 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who accessed 1 of the 4 modules4 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who accessed 3-4 modules2 Participants
SPIN-HAND ProgramIntervention Use: Number of Logins to the SPIN-HAND Program and Number of Participants Who Accessed SPIN-HAND Program Online FeaturesNumber of participants who used the goal-setting feature4 Participants
Primary

Participant Grade on Usability of the SPIN-HAND Program Based on Post-trial Patient Interviews

At 3-months post-randomization, qualitative semi-structured interviews were conducted with participants in the intervention arm to assess user acceptability and satisfaction. The interview, consisting of 29 questions, was guided by items of the Patient Education Materials Assessment Tool for Audiovisual Materials and addressed topics related to usability, understandability, organization, and clarity. During these interviews, participants were asked to give the SPIN-HAND program a grade ranging from 0-10, 0 being the worst and 10 being the best possible score. In this table, we report the overall mean grade reported by the intervention arm participants who agreed to be interviewed post-trial.

Time frame: 3 months

Population: Of the 15 intervention arm participants, 6 participated in the interview. Of the 9 participants who were not interviewed, 1 withdrew a few days after consenting to the feasibility trial, 3 were unreachable at 3-month post-randomization (3 contact attempts), 5 declined (2 participants indicated that they did not use the program enough, 2 declined due to health problems, 1 mentioned exercise was not a priority). None of the participants randomized to usual care participated in these interviews.

ArmMeasureValue (MEAN)Dispersion
SPIN-HAND ProgramParticipant Grade on Usability of the SPIN-HAND Program Based on Post-trial Patient Interviews8.5 Overall mean grade for SPIN-HAND programStandard Deviation 1.5
Primary

Usage Log Data: Completeness of the Automatic Usage Log Data Values Collected

Here we report our success in collecting participant usage log data. This is reported as the percentage of the usage log data that was successfully collected.

Time frame: 3 months

Population: None of the participants randomized to usual care logged into the SPIN-HAND program

ArmMeasureValue (NUMBER)
SPIN-HAND ProgramUsage Log Data: Completeness of the Automatic Usage Log Data Values Collected100 Percent completeness of usage log data
Primary

Usage Log Data: Linking of Data From the SPIN Cohort and SPIN-HAND Platforms.

We report our percentage success in linking data coming from the SPIN Cohort and SPIN-HAND platforms.

Time frame: 3 months

Population: None of the participants randomized to usual care logged into the SPIN-HAND program

ArmMeasureValue (NUMBER)
SPIN-HAND ProgramUsage Log Data: Linking of Data From the SPIN Cohort and SPIN-HAND Platforms.100 % success linking participant data
Secondary

EuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per Level

The EuroQol Group 5 Dimension 5 Level (EQ-5D-5L) is standardized questionnaire measuring 5 dimensions related to health related quality of life, mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. For each dimension, items are rated from 1 (no problems) to 5 (extreme problems). Here we report the number of intervention arm and control arm participants who gave scores ranging 1-5 for the different dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression), at baseline and at 3-months post randomization.

Time frame: Baseline, 3 months

Population: Of the 40 participants, 26 (65%) completed their 3-months follow-up assessments, including 14 in the intervention arm (58%) and 12 in the control arm (75%).

ArmMeasureGroupCategoryValue (COUNT_OF_PARTICIPANTS)
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 34 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 28 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 38 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 41 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 15 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 27 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 30 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 42 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 110 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 29 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 17 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 40 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 51 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 18 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 23 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 32 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 41 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 16 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 28 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 38 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 42 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 14 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 26 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 32 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 42 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 12 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 210 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 39 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 43 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 11 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 25 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 35 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 43 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 18 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 211 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 33 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 42 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 50 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 111 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 22 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 31 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 40 Participants
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 310 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 15 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 12 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 26 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 41 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 33 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 25 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 42 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 40 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - BaselineLevel 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 34 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 17 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 21 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 41 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 32 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 42 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelMobility - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 31 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 17 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 11 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 27 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 15 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 31 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 24 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 41 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 16 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - BaselineLevel 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 38 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 14 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 28 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 27 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 43 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 31 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 40 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - BaselineLevel 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelSelf care - Month 3Level 50 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 33 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 10 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 10 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 28 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - Month 3Level 24 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 35 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelPain/Discomfort - Month 3Level 22 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 43 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelAnxiety/Depression - BaselineLevel 40 Participants
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Number of Participants Per Dimension Per LevelUsual activity - BaselineLevel 50 Participants
Secondary

EuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated Health

As part of the EQ-5D-5L questionnaire, a Visual Analogue Scale (VAS) records the patient's self-rated health on a scale from 0-100 where the endpoints are labelled 'the best health you can imagine' (100) and 'the worst health you can imagine' (0). Here we report the mean (and standard deviations) self-reported patient health VAS scores of intervention arm participants and control arm participants (i.e. usual care), at baseline and at 3-months post-randomization.

Time frame: Baseline, 3 months

Population: Of the 40 participants, 26 (65%) completed their 3-months follow-up assessments, including 14 in the intervention arm (58%) and 12 in the control arm (75%).

ArmMeasureGroupValue (MEAN)Dispersion
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated HealthBaseline64.9 score on a scaleStandard Deviation 19.7
SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated HealthMonth 366.9 score on a scaleStandard Deviation 19.8
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated HealthBaseline56.8 score on a scaleStandard Deviation 15.9
Not Offered the SPIN-HAND ProgramEuroQol Group 5 Dimension 5 Level (EQ-5D-5L): Visual Analogue Scale (VAS) Scores for Patient Self-rated HealthMonth 354.9 score on a scaleStandard Deviation 13.1
Secondary

Patient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0

Measures 8 domains of health status with 4 items for each of 7 domains (physical function, anxiety, depression, fatigue, sleep disturbance, social roles and activities, pain interference) plus a single item for pain intensity. Items are scored on a 5-point scale (range 1-5), with different response options for different domains, and the single pain intensity item is measured on an 11-point rating scale. Higher scores represent more of the domain being measured; that is, better physical function and ability to participate in social roles and activities, but higher levels of anxiety, depression, fatigue, sleep disturbance, pain interference, and pain intensity. Total raw scores are obtained by summing item scores for each domain, which are converted into T-scores standardized from the general US population (mean=50, SD=10). Here, we report the pre- and post-intervention total scores for PROMIS-29 domains.

Time frame: Baseline, 3 months

Population: Of the 40 participants, 26 (65%) completed their 3-months follow-up assessments, including 14 in the intervention arm (58%) and 12 in the control arm (75%).

ArmMeasureGroupValue (MEAN)Dispersion
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Physical Function Domain- Baseline40.7 T-scoreStandard Deviation 8.9
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Physical Function Domain- Month 342.2 T-scoreStandard Deviation 8.6
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Anxiety Domain- Baseline53.8 T-scoreStandard Deviation 10.5
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Anxiety Domain- Month 348.7 T-scoreStandard Deviation 8.2
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Depression Domain- Baseline51.8 T-scoreStandard Deviation 10.1
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Depression Domain- Month 347.4 T-scoreStandard Deviation 8
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Fatigue Domain- Baseline58.3 T-scoreStandard Deviation 12
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Fatigue Domain- Month 355.7 T-scoreStandard Deviation 10.7
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Sleep Domain- Baseline54.3 T-scoreStandard Deviation 8.7
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Sleep Domain- Month 350.4 T-scoreStandard Deviation 6.7
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Social Roles Domain- Baseline46.0 T-scoreStandard Deviation 8.7
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Social Roles Domain- Month 349.5 T-scoreStandard Deviation 10
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Interference Domain- Baseline57.7 T-scoreStandard Deviation 9.9
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Interference Domain- Month 356.1 T-scoreStandard Deviation 7.8
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Intensity Domain- Baseline4.7 T-scoreStandard Deviation 2.8
SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Intensity Domain- Month 34.9 T-scoreStandard Deviation 2.7
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Intensity Domain- Month 35.3 T-scoreStandard Deviation 1.9
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Physical Function Domain- Baseline39.4 T-scoreStandard Deviation 6.5
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Sleep Domain- Baseline53.6 T-scoreStandard Deviation 9.6
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Physical Function Domain- Month 341.1 T-scoreStandard Deviation 6.6
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Interference Domain- Baseline61.7 T-scoreStandard Deviation 5.9
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Anxiety Domain- Baseline56.7 T-scoreStandard Deviation 9.9
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Sleep Domain- Month 354.3 T-scoreStandard Deviation 6.1
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Anxiety Domain- Month 353.2 T-scoreStandard Deviation 9.6
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Intensity Domain- Baseline5.9 T-scoreStandard Deviation 1.9
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Depression Domain- Baseline53.7 T-scoreStandard Deviation 9.9
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Social Roles Domain- Baseline42.3 T-scoreStandard Deviation 7.8
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Depression Domain- Month 351.6 T-scoreStandard Deviation 9.8
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Pain Interference Domain- Month 360.6 T-scoreStandard Deviation 6.7
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Fatigue Domain- Baseline59.3 T-scoreStandard Deviation 7.4
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Social Roles Domain- Month 340.7 T-scoreStandard Deviation 8.2
Not Offered the SPIN-HAND ProgramPatient Reported Outcomes Measurement Information System (PROMIS-29) Profile Version 2.0PROMIS-29 Fatigue Domain- Month 358.7 T-scoreStandard Deviation 8.9
Secondary

The Cochin Hand Function Scale (CHFS)

The Cochin Hand Function Scale (CHFS) measures functional ability of the hand among patients with rheumatic diseases. The 18-item CHFS measures ability to perform daily hand-related activities (e.g., kitchen, dressing oneself, hygiene, writing/typing). Items are scored on a 0-5 Likert scale (0=without difficulty; 5=impossible). Higher scores indicate less functionality. The total score is obtained by adding the scores of all items (range 0-90).

Time frame: Baseline, 3 months

Population: Of the 40 participants, 26 (65%) completed their 3-months follow-up assessments, including 14 in the intervention arm (58%) and 12 in the control arm (75%).

ArmMeasureGroupValue (MEAN)Dispersion
SPIN-HAND ProgramThe Cochin Hand Function Scale (CHFS)Baseline21.9 units on a scaleStandard Deviation 15.5
SPIN-HAND ProgramThe Cochin Hand Function Scale (CHFS)Month 322.0 units on a scaleStandard Deviation 15.5
Not Offered the SPIN-HAND ProgramThe Cochin Hand Function Scale (CHFS)Baseline21.1 units on a scaleStandard Deviation 16.1
Not Offered the SPIN-HAND ProgramThe Cochin Hand Function Scale (CHFS)Month 320.9 units on a scaleStandard Deviation 6.6

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026