NCT07022808 Tele-Exercise to Promote Empowered Movement in Individuals With Spinal Cord Injury
| NCT ID | NCT07022808 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Drexel University |
| Condition | Spinal Cord Injury |
| Study Type | INTERVENTIONAL |
| Enrollment | 200 participants |
| Start Date | 2026-05-04 |
| Primary Completion | 2029-01-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 200 participants in total. It began in 2026-05-04 with a primary completion date of 2029-01-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
To achieve our specific aims and hypotheses we will conduct a parallel group mixed methods randomized control trial comparing participation in the TEEMS program with exercise via asynchronous video library equivalent (control). The use of mixed methods will allow for the integration of quantitative findings with the qualitative, lived perspective of participants to provide a comprehensive analysis of the tele-exercise program outcomes. All aspects of the study from recruitment, screening, data collection, tele-exercise delivery and team meetings will be virtual to promote access and inclusion by removing barriers and promoting engagement. This study will compare our live group TEEMS program with individual pre-recorded exercise videos. We created TEEMS with the intention of maximizing exercise independence for participants, which decreases need for caregivers during physical activity. The design and participation in TEEMS is meant to increase personal factors that facilitate participation in exercise. These personal factors include confidence and positive associations with exercise. When these personal factors are targeted, individuals with SCI are more likely to participate in physical activity, which supports overall health and QoL.
Eligibility Criteria
Inclusion Criteria: 1. at least 12 months post SCI (motor spinal level C5 or below) 2. between 18-75 years of age 3. ability to elevate shoulders \>25% range 4. use assistive technology for mobility 5. not currently receiving structured rehabilitation (i.e. new episode of inpatient or outpatient rehabilitation services to treat a new or exacerbated mobility issue. Individuals attending outpatient services for ongoing wellness reasons are eligible to participate). 6. screened and medically cleared (if appropriate) for participation using the American College of Sports Medicine (ACSM) Preparticipation Health Screening Tool. The ACSM Health Screen helps to determine if an individuals should seek a medical referral prior to participation in exercise. The guideline for the screening are based on (1) current exercise participation, (2) history and symptoms of cardiovascular, metabolic, or renal disease, and (3) desired exercise intensity. The algorithm is based on risk stratification and minimizing the barriers of exercise participation by decreasing the number of unnecessary medical referrals. For this study and the safety of participants, those who need a medical referral based on the ACSM preparticipation health screen will be required to provide documentation of medical clearance from their primary medical provider prior to study participation. Dr. York will review screening information and medical clearances to ensure safe inclusion. 7. internet access to attend synchronous exercise classes Exclusion Criteria: 1. Known or suggestive cardiovascular, metabolic, and/or renal disease and/or presence of absolute or relative contraindications to exercise participation that is considered unsafe by their medical team 2. self-report previous hospitalization within a month, 3. self report active pressure injury 4. self report recent osteoporotic fracture 5. self-report uncorrectable vision loss, 6. self-report preexisting neurological conditions other than SCI
Contact & Investigator
Margaret Finley, PT, PhD
PRINCIPAL INVESTIGATOR
Drexel University
Frequently Asked Questions
Who can join the NCT07022808 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Spinal Cord Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07022808 currently recruiting?
Yes, NCT07022808 is actively recruiting participants. Contact the research team at SCIexerciseonline@drexel.edu for enrollment information.
Where is the NCT07022808 trial being conducted?
This trial is being conducted at Philadelphia, United States.
Who is sponsoring the NCT07022808 clinical trial?
NCT07022808 is sponsored by Drexel University. The principal investigator is Margaret Finley, PT, PhD at Drexel University. The trial plans to enroll 200 participants.