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Powered Seating Function Usage Among Veterans - Compliance and Coaching

Powered Seating Function Usage Among Veterans - Compliance and Coaching

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00839098
Enrollment
28
Registered
2009-02-09
Start date
2011-11-30
Completion date
2014-11-30
Last updated
2016-02-04

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

Conditions

Use of Power Wheelchairs and Power Seat Functions

Keywords

power wheelchairs, assistive technology, rehabilitation

Brief summary

The purpose of this randomized control study is to evaluate the use of electric powered wheelchairs and powered seating function patterns of Veterans to determine how usage patterns relate to activity, participation, and seating discomfort. In addition, it will be determined if a training program or a training program with a virtual coach will improve compliance of clinical practice guidelines for pressure relief, upper limb preservation, and discomfort management. The virtual coach is a portable, programmable intelligent reminder designed to enhance a person's use of their power wheelchair and power seat functions.

Detailed description

This is a randomized control trial evaluating power seat function usage among 3 groups: 1) standard of care- verbal instruction 2) verbal and written instruction and 3) same as #2 with addition of virtual coach. This study will be conducted in two phases. Phase I data will be collected for 8 weeks, during the time period that the subject is awaiting for delivery of their personal electric powered wheelchair (EPW) with powered seat functions. Phase II data will be collected for a total of 4 weeks, after the subject receives their personal wheelchair. During Phase I, Visit I, subjects will be fitted for a study EPW with powered seat functions. All subjects will be provided with the standard of care training on driving of the wheelchair and usage of the power seating functions. Subjects will be instructed to go about their daily activities as they normally would, while the instrumented wheelchair will track their usage of the wheelchair and seating habits. Phase I, Visit II-IV, subjects will be randomized into one of three study groups: Control Group; Instruction Group; and Instruction & Virtual Coach Group. Subjects assigned to the Control Group will receive 'standard of care.' Subjects assigned to the Intervention Group will receive the standard of care and additional written instructional materials and feedback regarding activity and wheelchair usage. Subjects assigned to the Instruction & Virtual Coach Group will receive the same training and instructional materials as the Intervention Group. This group will also be instructed in use of the virtual coach system, which will be active during the in-home usage periods to provide personalized feedback. Phase II will involve mounting a wheelchair and seat function usage datalogger to the subject's personal wheelchair over a period of 4 weeks.

Interventions

OTHERInstruction Group: Power seat function usage instruction- verbal and written instruction

Subjects assigned to the Intervention Group will be assigned to an Intervention Group Clinician. The Intervention Group Clinicians will provide the same training as the Control Group Clinicians, with the addition of discussing the Veteran's activity and seating function usage data, reviewing and providing a study pamphlet and compact disk as a reference guide on use of power seat functions.

OTHERInstruction and Virtual Coach Group: Power seat function usage instruction- verbal, written, and virtual coach

Subjects assigned to the Instruction & Virtual Coach Group will be assigned to an Intervention Group Clinician and will receive the same training and instructional materials as the Instruction Group. Subjects will also be instructed in use of the virtual coach system, which will be active during the in-home usage periods to provide personalized feedback. As the Virtual Coach is a dynamic intelligent system, it will adjust its coaching to the needs of the individual. For example, if the person is compliant, the Virtual Coach will give positive feedback and then gradually transition to operating quietly in the background. If a person is not fully compliant, it will alter feedback modes (e.g., verbal cues, auditory tones, visual cues) and timing to attempt to increase compliance.

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

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

Inclusion criteria

* Subjects must be 18 years of age or older. * A power wheelchair with power seat functions must be recommended as medically necessary by a qualified clinician with ATP credential or board certified in physical medicine and rehabilitation from the VAPHS Wheelchair and Seating Clinic or the Center for Assistive Technology. * Subjects must be able to be properly fitted with one of the study EPWs; 18 or 20 seat widths will be available. Cushions and backrests will be made available to meet subject's clinical needs. * Subject's home must be accessible to accommodate use of a power w/c. * Subject must be determined to be fully capable of examining his/her sitting surface daily for redness or pressure ulcers or if not that another individual can be designated as able and willing to-do this.

Exclusion criteria

* Subjects who have active pelvic, gluteal or thigh wounds or who have had a pressure ulcer in these regions within the past 30 days. (They may be worsened by prolonged sitting). * Subjects who report more than 5 days of hospitalization in the previous month. (They may not spend enough time using an EPW with powered seating functions).

Design outcomes

Primary

MeasureTime frameDescription
Compliance RateEvery 2 weeks for 8 weeks following acquisition of wheelchairCompliance rate is a measure of compliance with the recommendation of using powered seating functions (moderate or maximum range of tilt, at least once every hour, for 2 minutes). The participant had to follow the recommended position, duration, and frequency to be considered as compliant and performed successful repositioning exercise. The compliance rate of a participant was the number of successful repositioning exercise divided by the sum of the number of successful repositioning exercise and missed repositioning exercise. The result of the difference between the baseline and week 7-8 (last 2 weeks) was shown here.
Frequency of Power Seat Function UsageEvery 2 weeks for 8 weeks following acquisition of wheelchairFrequency of power seat function usage was measured by the number of times of changing tilt and recline angles averaged by the duration that the participant occupied the wheelchair per day. The results of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.
Power Wheelchair UsageEvery 2 weeks for 8 weeks following acquisition of wheelchairPower wheelchair usage was measured by the sum of distances that the power wheelchair traveled (km) divided by the duration of the wheelchair being occupied a day (hr). The result of the difference between the baseline and week 7-8 (last 2 weeks) was shown here.
Wheelchair OccupancyEvery 2 weeks for 8 weeks following acquisition of wheelchairWheelchair occupancy was measured by the sum of duration that the seat of the wheelchair was occupied. The results of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.

Secondary

MeasureTime frameDescription
Questionnaire Responses: Psychological Impacts of Assistive Devices ScaleAt the end of every two weeksThis tool is to measure perceived psychological impact of using an assistive device. It consists of three subscales, Competence (12 items), Adaptability (6 items), and Self-esteem (8 items). Each item is scored on a likert scale from -3 (decreases) to + 3 (increases). The total score is the sum of all 26 items, ranging from -78 to 78. A higher positive score indicates more positive impact. A negative score indicates negative impact. The differences between the measurements taken at the end of 2nd week (end of baseline) and the end of 8th week (end of intervention period) are reported here to show the intervention effect.
Questionnaire Responses: Independence in CommunityAt the end of 2nd (end of baseline) week and 8th week (end of intervention period) following acquisition of wheelchairThis outcome was measured in three aspects: Physical Independence, Cognitive Independence, and Mobility, using the three of the subscales of Craig Handicap Assessment and Reporting Technique Scale. The scores of each subscale has to be calculated with specific formula and weight based on the manual. The range of each subscale score are: Physical Independence: 28-100; Cognitive Independence: 15-100; and Mobility: 16-100. A higher score indicates greater independence. The analyzed results of the difference between the measurements at the end of 2nd week and 8th week were shown here.
Questionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)Every 2 weeks for 8 weeks following acquisition of wheelchairGeneral Discomfort Assessment (GD) and Discomfort Intensity Rating (DI) are two sub-scales of TAWC. Higher scores indicate greater discomfort. GD consists of 8 discomfort statements and 5 comfort statements. The statements are rated on a seven point Likert scale, from strongly disagree to strongly agree of points from 1-7 (total score: 13-91). DI includes seven body areas (back, neck, buttocks, legs, arms, feet, and hands) and overall discomfort level, rated for a degree of discomfort intensity on a scale of 0 (no discomfort) to 10 (severe discomfort). Space is also included for the user to list additional body areas. DI scores may range from 0 to more than 80, depending on whether the participant reported additional areas of discomfort. Although GD and DI were measured daily, the data were average for each two-week period. The average GD and DI of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.

Countries

United States

Participant flow

Participants by arm

ArmCount
Control Group
Control Group
3
Instruction Group
Instruction Group Instruction Group: Power seat function usage instruction- verbal and written instruction: Subjects assigned to the Intervention Group will be assigned to an Intervention Group Clinician. The Intervention Group Clinicians will provide the same training as the Control Group Clinicians, with the addition of discussing the veteran's activity and seating function usage data, reviewing and providing a study pamphlet and compact disk as a reference guide on use of power seat functions.
12
Instruction and Virtual Coach Group
Instruction and Virtual Coach Group Instruction and Virtual Coach Group: Power seat function usage instruction- verbal, written, and virtual coach: Subjects assigned to the Instruction & Virtual Coach Group will be assigned to an Intervention Group Clinician and will receive the same training and instructional materials as the Instruction Group. Subjects will also be instructed in use of the virtual coach system, which will be active during the in-home usage periods to provide personalized feedback. As the Virtual Coach is a dynamic intelligent system, it will adjust its coaching to the needs of the individual. For example, if the person is compliant, the Virtual Coach will give positive feedback and then gradually transition to operating quietly in the background. If a person is not fully compliant, it will alter feedback modes (e.g., verbal cues, auditory tones, visual cues) and timing to attempt to increase compliance.
13
Total28

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyWithdrawal by Subject217

Baseline characteristics

CharacteristicInstruction GroupInstruction and Virtual Coach GroupControl GroupTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
1 Participants4 Participants0 Participants5 Participants
Age, Categorical
Between 18 and 65 years
11 Participants9 Participants3 Participants23 Participants
Age, Continuous53.4 Years of age
STANDARD_DEVIATION 9.1
54.5 Years of age
STANDARD_DEVIATION 17
47.0 Years of age
STANDARD_DEVIATION 19.9
53.2 Years of age
STANDARD_DEVIATION 14
Region of Enrollment
United States
12 participants13 participants3 participants28 participants
Sex: Female, Male
Female
5 Participants5 Participants2 Participants12 Participants
Sex: Female, Male
Male
7 Participants8 Participants1 Participants16 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —
other
Total, other adverse events
0 / 30 / 120 / 13
serious
Total, serious adverse events
0 / 30 / 120 / 13

Outcome results

Primary

Compliance Rate

Compliance rate is a measure of compliance with the recommendation of using powered seating functions (moderate or maximum range of tilt, at least once every hour, for 2 minutes). The participant had to follow the recommended position, duration, and frequency to be considered as compliant and performed successful repositioning exercise. The compliance rate of a participant was the number of successful repositioning exercise divided by the sum of the number of successful repositioning exercise and missed repositioning exercise. The result of the difference between the baseline and week 7-8 (last 2 weeks) was shown here.

Time frame: Every 2 weeks for 8 weeks following acquisition of wheelchair

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureValue (MEAN)Dispersion
Arm 2: Instruction GroupCompliance Rate8.9 Percentage of participants' complianceStandard Deviation 15.9
Arm 3: Instruction + VSC GroupCompliance Rate39.7 Percentage of participants' complianceStandard Deviation 23.5
p-value: 0.27Wilcoxon (Mann-Whitney)
Primary

Frequency of Power Seat Function Usage

Frequency of power seat function usage was measured by the number of times of changing tilt and recline angles averaged by the duration that the participant occupied the wheelchair per day. The results of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.

Time frame: Every 2 weeks for 8 weeks following acquisition of wheelchair

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureGroupValue (MEAN)Dispersion
Arm 2: Instruction GroupFrequency of Power Seat Function UsageFreq of mod & max tilt (times/hr): Difference.51 times/hourStandard Deviation 2.52
Arm 2: Instruction GroupFrequency of Power Seat Function UsageFreq of mod & max recline (times/hr): Difference-0.43 times/hourStandard Deviation 1.36
Arm 3: Instruction + VSC GroupFrequency of Power Seat Function UsageFreq of mod & max tilt (times/hr): Difference0.03 times/hourStandard Deviation 2.51
Arm 3: Instruction + VSC GroupFrequency of Power Seat Function UsageFreq of mod & max recline (times/hr): Difference0.09 times/hourStandard Deviation 0.15
p-value: >0.05Wilcoxon (Mann-Whitney)
Primary

Power Wheelchair Usage

Power wheelchair usage was measured by the sum of distances that the power wheelchair traveled (km) divided by the duration of the wheelchair being occupied a day (hr). The result of the difference between the baseline and week 7-8 (last 2 weeks) was shown here.

Time frame: Every 2 weeks for 8 weeks following acquisition of wheelchair

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureValue (MEAN)Dispersion
Arm 2: Instruction GroupPower Wheelchair Usage0.17 km/hourStandard Deviation 0.45
Arm 3: Instruction + VSC GroupPower Wheelchair Usage-0.04 km/hourStandard Deviation 0.08
p-value: >0.05Wilcoxon (Mann-Whitney)
Primary

Wheelchair Occupancy

Wheelchair occupancy was measured by the sum of duration that the seat of the wheelchair was occupied. The results of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.

Time frame: Every 2 weeks for 8 weeks following acquisition of wheelchair

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureValue (MEAN)Dispersion
Arm 2: Instruction GroupWheelchair Occupancy-.07 hoursStandard Deviation 1.9
Arm 3: Instruction + VSC GroupWheelchair Occupancy-0.4 hoursStandard Deviation 1.8
p-value: >0.05Wilcoxon (Mann-Whitney)
Secondary

Questionnaire Responses: Independence in Community

This outcome was measured in three aspects: Physical Independence, Cognitive Independence, and Mobility, using the three of the subscales of Craig Handicap Assessment and Reporting Technique Scale. The scores of each subscale has to be calculated with specific formula and weight based on the manual. The range of each subscale score are: Physical Independence: 28-100; Cognitive Independence: 15-100; and Mobility: 16-100. A higher score indicates greater independence. The analyzed results of the difference between the measurements at the end of 2nd week and 8th week were shown here.

Time frame: At the end of 2nd (end of baseline) week and 8th week (end of intervention period) following acquisition of wheelchair

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureGroupValue (MEAN)Dispersion
Arm 2: Instruction GroupQuestionnaire Responses: Independence in CommunityPhy. Independence: Difference9.5 units on a scaleStandard Deviation 55.6
Arm 2: Instruction GroupQuestionnaire Responses: Independence in CommunityCog. Independence: Difference19.3 units on a scaleStandard Deviation 38.2
Arm 2: Instruction GroupQuestionnaire Responses: Independence in CommunityMobility: Difference0 units on a scaleStandard Deviation 22.5
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Independence in CommunityPhy. Independence: Difference8.6 units on a scaleStandard Deviation 49.2
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Independence in CommunityCog. Independence: Difference-11.7 units on a scaleStandard Deviation 18.3
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Independence in CommunityMobility: Difference0.5 units on a scaleStandard Deviation 17.2
p-value: >0.05Wilcoxon (Mann-Whitney)
Secondary

Questionnaire Responses: Psychological Impacts of Assistive Devices Scale

This tool is to measure perceived psychological impact of using an assistive device. It consists of three subscales, Competence (12 items), Adaptability (6 items), and Self-esteem (8 items). Each item is scored on a likert scale from -3 (decreases) to + 3 (increases). The total score is the sum of all 26 items, ranging from -78 to 78. A higher positive score indicates more positive impact. A negative score indicates negative impact. The differences between the measurements taken at the end of 2nd week (end of baseline) and the end of 8th week (end of intervention period) are reported here to show the intervention effect.

Time frame: At the end of every two weeks

Population: Only the data of the participants who completed the study protocol and use the wheelchair were included in the data analysis.

ArmMeasureValue (MEAN)Dispersion
Arm 2: Instruction GroupQuestionnaire Responses: Psychological Impacts of Assistive Devices Scale11.1 units on a scaleStandard Deviation 17.7
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Psychological Impacts of Assistive Devices Scale-8.4 units on a scaleStandard Deviation 15.6
p-value: 0.04Wilcoxon (Mann-Whitney)
Secondary

Questionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)

General Discomfort Assessment (GD) and Discomfort Intensity Rating (DI) are two sub-scales of TAWC. Higher scores indicate greater discomfort. GD consists of 8 discomfort statements and 5 comfort statements. The statements are rated on a seven point Likert scale, from strongly disagree to strongly agree of points from 1-7 (total score: 13-91). DI includes seven body areas (back, neck, buttocks, legs, arms, feet, and hands) and overall discomfort level, rated for a degree of discomfort intensity on a scale of 0 (no discomfort) to 10 (severe discomfort). Space is also included for the user to list additional body areas. DI scores may range from 0 to more than 80, depending on whether the participant reported additional areas of discomfort. Although GD and DI were measured daily, the data were average for each two-week period. The average GD and DI of the difference between the baseline and week 7-8 (last 2 weeks) were shown here.

Time frame: Every 2 weeks for 8 weeks following acquisition of wheelchair

ArmMeasureGroupValue (MEAN)Dispersion
Arm 2: Instruction GroupQuestionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)General Discomfort: Difference4.6 units on a scaleStandard Deviation 7.5
Arm 2: Instruction GroupQuestionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)Discomfort Index: Difference1.8 units on a scaleStandard Deviation 10
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)General Discomfort: Difference-7.4 units on a scaleStandard Deviation 16.9
Arm 3: Instruction + VSC GroupQuestionnaire Responses: Tool for Assessing Wheelchair Discomfort (TAWC)Discomfort Index: Difference-12.1 units on a scaleStandard Deviation 13.6
p-value: >0.05Wilcoxon (Mann-Whitney)

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