About this trial
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
Qualifiers
at least 12 months post SCI (motor spinal level C5 or below)
between 18-75 years of age
ability to elevate shoulders >25% range
use assistive technology for mobility
Disqualifiers
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
self-report previous hospitalization within a month,
self report active pressure injury
self report recent osteoporotic fracture
Trial design
Treatments tested in this trial
- Synchronous Group exercise
- Asynchronous exercise (Control)
Treatment groups
Sponsors and collaborators
Drexel University
Lead sponsor
United States Department of Defense
Collaborator