Using an Adaptive Rower for People Using Motorized Wheelchairs
1 other identifier
interventional
12
1 country
2
Brief Summary
The goal of this clinical trial are to determine the feasibility and impact of an adaptive rower exercise intervention for adults who use motorized wheelchairs for mobility. The main question\[s\] it aims to answer are:
- 1.What is the impact on participant's cardiovascular endurance, and perception of mobility and quality of life?
- 2.Is the intervention feasible, acceptable and safe?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2024
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 2, 2024
CompletedFirst Posted
Study publicly available on registry
August 9, 2024
CompletedStudy Start
First participant enrolled
August 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 31, 2025
CompletedFebruary 24, 2026
February 1, 2026
10 months
August 2, 2024
February 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Six Minute Arm Test
Submaximal fitness test using an upper body ergometer. Maximum power, maximum rate of perceived exertion and maximum heart rate are recorded. Higher power, lower RPE and lower maximum heart rate is better outcome
Study Start (Week 1) and at Study Completion (week 7-8)
Spinal Cord Injury Functional Inventory basic mobility, motorized wheelchair mobility and resilience subscales
Scores from 0-100% where mean scores for population is 50%, higher score better outcome
Study Start (Week 1) and at Study Completion (week 7-8)
Secondary Outcomes (5)
System Usability Scale
Study Completion (week 7-8)
Physical Activity Enjoyment Scale-Short (PACES-S)
Study Completion (week 7-8)
Heart Rate (beats per minute), mean and range at rest, mean and range during rowing
2 x a week through study completion, 7-8 weeks
Rate of Perceived Exertion (RPE)-Borg 6-20 Scale
2 x a week through study completion, 7-8 weeks
Pain Scale (0-10 visual analog scale) and body location of pain verbalized by participant and recorded by study personnel
2 x a week through study completion, 7-8 weeks
Other Outcomes (1)
Short Self-Efficacy for Exercise Scale
Study Start (Week 1) and at Study Completion (week 7-8)
Study Arms (1)
Single Group Intervention Arm - Adaptive Rowing
EXPERIMENTAL12 supervised and coached sessions of 10-20 minutes of moderate to vigorous exercise using an adaptive rower.
Interventions
12 supervised and coached sessions of 10-20 minutes of moderate to vigorous exercise using an adaptive rower.
Eligibility Criteria
You may qualify if:
- Use a motorized wheelchair for mobility
- Able to perform a rowing motion with upper extremities with or without grip aids
You may not qualify if:
- Existing pressure sores
- Increasing pain with rowing motion
- Unstable angina
- Uncontrolled arrythmia
- Acute illness with fever
- Blood pressure above 180/100 mmHg
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Public Health Research Center
Columbia, South Carolina, 29208, United States
Still Hopes Retirement Community
West Columbia, South Carolina, 29169, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Assistant Professor
Study Record Dates
First Submitted
August 2, 2024
First Posted
August 9, 2024
Study Start
August 15, 2024
Primary Completion
May 31, 2025
Study Completion
May 31, 2025
Last Updated
February 24, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Data will be available after completion of the study when dissemination occurs; and will be available indefinitely
- Access Criteria
- website
De-identified data will be part of dissemination of project results and be shared on open science framework. Data shared would be basic demographics (age, sex), pre and post outcome measures (six minute arm test time, spinal cord functional index score, PROMIS Scales for wheelchair mobility and resilience), session data (minutes of rowing, minutes of rest time, RPE ratings, heart rate data, pain/soreness ratings)