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Using an Adaptive Rower for People Using Motorized Wheelchairs

Using an Adaptive Rower for People Using Motorized Wheelchairs to Improve Cardiovascular Fitness

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06546891
Enrollment
12
Registered
2024-08-09
Start date
2024-08-15
Completion date
2025-05-31
Last updated
2026-02-24

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

Conditions

People Who Use Motorized Wheelchairs for Mobility

Keywords

motorized wheelchair, exercise, adaptive fitness, rowing

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? examine feasibility of the adaptive rower intervention through measures of acceptability, adherence, intensity and safety for adults who use motorized wheelchairs for mobility. Participants will complete 12 sessions of 10-20 minutes of supervised and coached moderate to vigorous activity using the adaptive rower over a seven week period. Participants will complete pre- and post- outcome assessments of cardiovascular fitness, and outcome surveys,

Detailed description

A rolling prospective clinical trial with a target population of 10 participants in the Columbia, South Carolina area will evaluate the impact of the adaptive rower on cardiovascular fitness, participant perception and feasibility for people who use motorized wheelchairs. Participants will be screened for inclusion/exclusion criteria, perform initial outcome measures and instructions on rowing in the first visit, and then have 12 exercise sessions over 6 or 7 weeks, followed by a final visit for final outcome measures. All research will occur at the University of South Carolina Rehab Lab in the public health research center building. Over the 6-7 week intervention period, participants will exercise approximately two times per week, with two additional visits available in week 7 for any missed sessions to fulfill the 12-visit dosage. Session data will include measures of heart rate, 0-10 Borg rate of perceived exertion (RPE), and power output (rower output in watts). The session goal is to maintain moderate-vigorous intensities (5-8 on the Borg RPE scale) with individually modifiable intervals of work and rest with the goal of 10-20 minutes of moderate-vigorous physical activity total per session depending on the individual's initial fitness levels (as judged by self-reported activity level and performance on the initial six-minute arm test) and progressed as able. After completing the intervention period, participants will return for final evaluation.

Interventions

BEHAVIORALAdaptive Rowing

12 supervised and coached sessions of 10-20 minutes of moderate to vigorous exercise using an adaptive rower.

Sponsors

University of South Carolina
Lead SponsorOTHER
Foundation for Physical Therapy, Inc.
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single Group Case Series

Eligibility

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

Inclusion criteria

* Use a motorized wheelchair for mobility * Able to perform a rowing motion with upper extremities with or without grip aids

Exclusion criteria

* Existing pressure sores * Increasing pain with rowing motion * Unstable angina * Uncontrolled arrythmia * Acute illness with fever * Blood pressure above 180/100 mmHg

Design outcomes

Primary

MeasureTime frameDescription
Six Minute Arm TestStudy Start (Week 1) and at Study Completion (week 7-8)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
Spinal Cord Injury Functional Inventory basic mobility, motorized wheelchair mobility and resilience subscalesStudy Start (Week 1) and at Study Completion (week 7-8)Scores from 0-100% where mean scores for population is 50%, higher score better outcome

Secondary

MeasureTime frameDescription
System Usability ScaleStudy Completion (week 7-8)a standardized 10-question survey for perception of usability, scored from 0-100%, higher score, better outcome
Physical Activity Enjoyment Scale-Short (PACES-S)Study Completion (week 7-8)a standardized 4-question survey for perception of enjoyment of a physical activity intervention, scale is 1 (strongly disagree) to 5 (strongly agree), total score 4-20 with higher score as better outcome
Heart Rate (beats per minute), mean and range at rest, mean and range during rowing2 x a week through study completion, 7-8 weeksHeart rate will be recorded at rest and throughout the exercise intervention using a polar heart rate monitor and actigraph. Heart rate near target zone, better outcome
Rate of Perceived Exertion (RPE)-Borg 6-20 Scale2 x a week through study completion, 7-8 weeksRPE will be verbally stated by participant and recorded by study personnel at beginning, mid and end of steady state portion, and at each interval for interval exercise. (RPE, 6-20, higher means higher intensity) RPE within target zone of moderate intensity (12-14) better outcome
Pain Scale (0-10 visual analog scale) and body location of pain verbalized by participant and recorded by study personnel2 x a week through study completion, 7-8 weeksparticipant complaints of discomfort or pain verbally stated along with location. Higher means worse pain, lower is better outcome

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026