Using an Adaptive Rower for People Using Motorized Wheelchairs

University of South Carolina

Status: Enrolling

Conditions: People Who Use Motorized Wheelchairs for Mobility

Treatments: Behavioral: Adaptive Rowing

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06546891

Pro00137469

Details and patient eligibility

About

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,

Full 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.

Enrollment: 10 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

Single Group Intervention Arm - Adaptive Rowing

Experimental group

Description:

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

Treatment:

Behavioral: Adaptive Rowing