NCT06546891

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. 1.What is the impact on participant's cardiovascular endurance, and perception of mobility and quality of life?
  2. 2.Is the intervention feasible, acceptable and safe?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

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

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 9, 2024

Completed
6 days until next milestone

Study Start

First participant enrolled

August 15, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2025

Completed
Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

10 months

First QC Date

August 2, 2024

Last Update Submit

February 20, 2026

Conditions

Keywords

motorized wheelchairexerciseadaptive fitnessrowing

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

EXPERIMENTAL

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

Behavioral: Adaptive Rowing

Interventions

Adaptive RowingBEHAVIORAL

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

Single Group Intervention Arm - Adaptive Rowing

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Still Hopes Retirement Community

West Columbia, South Carolina, 29169, United States

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Single Group Case Series
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

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)

Time Frame
Data will be available after completion of the study when dissemination occurs; and will be available indefinitely
Access Criteria
website
More information

Locations