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Shoulder Prosthesis Telerehab Care Trial

The PROTECT-study: Home-based Telerehabilitation in the Post-operative Care After Shoulder Arthroplasty Compared to Usual Care: a Randomized Control Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05699031
Acronym
PROTECT
Enrollment
120
Registered
2023-01-26
Start date
2023-03-01
Completion date
2026-09-30
Last updated
2024-04-12

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

Conditions

REHABILITATION, SHOULDER ARTHROPLASTY, TELEREHABILITATION

Keywords

SHOULDER ARTHROPLASTY, REHABILITATION, TELEREHABILITATION

Brief summary

The goal of this clinical trial is to compare the rehabilitation by use of a smartphone-app with the usual care of physical therapy in patients, 60 years and older, who underwent a primary shoulder arthroplasty. The main questions it aims to answer are: * is the outcome of rehabilitation with the app as good as the usual care? * is the outcome for both types of shoulder arthroplasty similar? * what is the usability of the app?. Participants will * have treatment according to the group they are allocated to * fill in questionnaires at specific moments during the rehabilitation stage (0 - 3 months ) and at 1 year post-surgery

Interventions

DEVICEAPP

Patients allocated in the app-group will use the newly developed smartphone app te rehabilitate. 5 exercises are provided daily. Daily questionnaires will monitor exercise performance, VAS pain, household activities. Information modules will be sent at specific times.

OTHERPHYSICAL THERAPY

Patients allocated in the physio-group will go, twice a week, to a physical therapist of their choice to rehabilitate. The physical therapist will follow the general guidelines provided by the hospital (surgeon).

Sponsors

University Ghent
CollaboratorOTHER
University Hospital, Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* 60 years and older * primary total shoulder arthroplasty (anatomical and reverse) * osteoarthritis, cuff tear arthropathy, pseudoparalysis * return home after discharge from hospital * no brace after surgery * sufficient verbal and written comprehension * hospitalization insurance

Exclusion criteria

* revision arthroplasty * arthroplasty for fracture or tumor * neurological disease (parkinson, stroke, ...) * no access to smartphone, tablet or internet connectivity

Design outcomes

Primary

MeasureTime frameDescription
SHOULDER PAIN AND DISABILITY INDEX (SPADI)week 3Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder
SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline post-operativeweek 0Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder
SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline pre-operativePrior to surgeryContent: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

Secondary

MeasureTime frameDescription
SINGLE ASSESSMENT NUMERIC EVALUATION (SANE)Prior to surgery, week 3, week 6, week 12, week 52Content: 1 question: 'how would you rate your shoulder today as a percentage of normal?'. Scoring: percentage between 0 and 100% Interpretation: 100% being a normal shoulder.
GRONINGEN ACTIVITY RESTRICTION SCALE (GARS-4)Prior to surgery, week 3, week 6, week 12, week 52Content: 18 questions to identify problems with self-sufficiency in self-care and housekeeping. Patients do not respond if they do that activity but rather if they could do that activity. Scoring: ordinal scale from 1 (Yes, I can do that on my own without any effort) up to 4 (No, I can't do that on my own, but only with the help of others). Interpretation: A higher score (max 72) is related to a lower self-sufficiency.
EXERCISE ADHERENCE RATING SCALE (EARS)Prior to surgery, week 3, week 6, week 12, week 52Content: 3 sections section A: 6 questions to evaluate the prescribed exercises. section B: 6 questions on how a patient does the recommended exercises or activities. section C: 10 statements on why a patient does or does not do the recommended exercises or activities. Scoring: sections B and C: 5-point Likert scale (0 - 4) (some questions scored reversed). Interpretation: section B (range 0 - 24): a higher score indicates a better compliance/adherence . section C (range 0 - 40): a higher score indicates a better adherence.
EXERCISE DIARYDaily post-surgery (week 0 - week 12)Content: performed exercises, household activities, VAS pain. Diary on paper for physio-group, by the app for the app-group.
SELF-EFFICACY FOR EXERCISES (SEE)Week 3, week 6, week 12, week 52Content: 9 questions about 'confidence in engaging in exercise 3 times a week for 20 minutes if faced with a barrier'. Scoring: 'not very confident' (0) and 'very confident' (10). Interpretation: The higher the score , the patient feel more confident in performing prescribed exercises.
GLOBAL RATING OF CHANGE SCALE (GROC)Prior to surgery, week 3, week 6, week 12, week 52Content: A single question (How would you currently describe the change in your operated shoulder compared to just before surgery) is scored on a scale, ranging from 'very much worse' through 'unchanged' to 'completely recovered'. Scoring: The scale used is divided in 11 points ( very much worse -5, the same 0, very much better + 5) Interpretation: the number given indicates how a patient perceives the change after surgery.
GLOBAL PERCEIVED EFFECT (GPE/GEE)Prior to surgery, week 3, week 6, week 12, week 52Content: 2 questions: To what extent have you recovered from your symptoms?, How satisfied are you with your treatment?. Scoring: a 7-point rating scale. Interpretation: The higher the score , the better.
ACTIVE MOBILITY (ROM) OF THE SHOULDERPrior to surgery, week 3, week 6, week 12, week 52ACTIVE ROM: forward flexion and abduction with extended elbow, functional internal and external rotation in standing position. * maximal pain free ROM * forward flexion and abduction with extended elbow: measured with the EasyAngle (Meloq AB Sweden) * hand-to-back and hand-nek test : scored as in Constant-Murley Score 2\) PASSIVE: forward flexion, abduction, external and internal rotation in supine position. * maximal pain free ROM * forward flexion and abduction: measured with the EasyAngle (Meloq AB Sweden) * rotations: measured as ER1 (arm at the side)/ ER2 (arm in 90° abduction) and IR1 (arm in 90° forward flexion)/ IR2 (arm in 90° abduction) with the EasyAngle (Meloq AB Sweden).
PASSIVE MOBILITY (ROM) OF THE SHOULDERPrior to surgery, week 3, week 6, week 12, week 52PASSIVE: forward flexion, abduction, external and internal rotation in supine position. * maximal pain free ROM * forward flexion and abduction: measured with the EasyAngle (Meloq AB Sweden) * rotations: measured as ER1 (arm at the side)/ ER2 (arm in 90° abduction) and IR1 (arm in 90° forward flexion)/ IR2 (arm in 90° abduction) with the EasyAngle (Meloq AB Sweden).
STRENGTHPrior to surgery, week 3, week 6, week 12, week 52Forward flexion, extension, ab- and adduction, external and internal rotation. * isometrical contraction for 5 seconds, 3 repetitions, 30 sec break in between * measured with EasyForce (Meloq AB Sweden) * seated, both feet on the ground, back against backrest * elbow flexed (90°) held at side, fist forward, thumb upward
CONSTANT-MURLEY SCOREPrior to surgery, week 3, week 6, week 12, week 52Content: partially clinical (65 points) and partially PROM (35 points) assessed. Scoring: The formula to calculate the total score is: pain (0-15) + ADL (4x (0-5) = 0-20) + mobility (4 x (0-10) = 0-40) + strength (0 -25). Strength will be measured with the arm elevated to 90 ° in the scapular plane using an IDOmeter. Interpretation: 0-55 points = bad, 56-70 points = mediocre, 71-85 points = good, 86-100 points = excellent score
ACTIVITIES OF DAILY LIVING EXTERNAL AND INTERNAL ROTATIONS (ADLEIR)Prior to surgery, week 3, week 6, week 12, week 52Content: 12 questions about specific ADL tasks that require external or internal rotation while performing. Scoring: Each activity is scored between 0 (unable to do) and 3 (not difficult at all). All activities should be performed without the help of flexing the neck or bending the trunk and without the help of first abducting the elbow (i.e., without doing a hornblower sign). Interpretation: The maximal score is 36. A higher score means that the patient is able to perform ADL activities with enough strength in external and internal rotation
EUROQOL 5-DIMENSIONS 5-LEVEL (EQ-5D-5L)Prior to surgery, week 3, week 6, week 12, week 52Content: 5 questions + EQ-5D VAS for general health. Scoring: 5-response scale (from 'no problems' to 'extreme problems') + VAS percentage between 0 (worst imaginable health state) and 100 (best imaginable health state). Interpretation: VAS score for general health indicates how a patient perceives his general health, Other questions are descriptive for problems in mobility, self-care, usual activities, pain/ discomfort, anxiety/depression.

Other

MeasureTime frameDescription
GENDERPre-surgeryContent: specify gender of participant
DIAGNOSTICSPre-surgeryContent: specify why patient needed a shoulder arthroplasty
SINGLE EASE QUESTION (SEQ)Week 12Content: 1 question to assess how difficult users find a task. Scoring: 7-point rating scale ranging from very difficult (1) to very easy (7). Interpretation: The average SEQ score is 5.5 (between 5.3 and 5.6). It is advised to ask a more detailed information/ explanation if a score \<5 is given.
M-HEALTH APP USABILITY QUESTIONNAIRE (MAUQ)Week 12Content: 21 questions in 3 categories: ease of use and satisfaction, system information arrangement, usefulness (version for interactive app, user patient and provider). Scoring: between 1 (strongly disagree) and 7 (strongly agree) =\> average score. Interpretation: the higher the score the higher the usability.
SYSTEM USABILITY SCALE (SUS)Week 12Content: 10 questions about system satisfaction, usability and learnability. Scoring: 5 response options ranging from strongly disagree (1) to strongly agree (5). Interpretation: A score above 68 (/100) is considered above average, while a score lower than 68 is considered a below average score.
AGEPre-surgeryContent: specify age of participant

Countries

Belgium

Contacts

Primary ContactDominiek Vandenbosch, MSc
dominiek.vandenbosch@ugent.be+32 9 332 16 69

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026