Actively Recruiting
Precision-based Teleexercise Trial to Increase Adherence in People With Disabilities
Led by University of Alabama at Birmingham · Updated on 2026-01-09
257
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how to best increase physical activity in people with mobility impairments through a 32-week program using a design called SMART (Sequential Multiple Assignment Randomized Trial). This approach tests the best way to combine teleexercise with predictive analytics to adapt the support participants receive based on their exercise adherence. The study aims to find effective strategies for improving activity levels while exploring factors that influence outcomes and testing the accuracy of prediction methods. Participants first complete a run-in period including consent, surveys, and setup of an exercise tracker and band. They are then randomly assigned to either an Asynchronous Exercise Program (AEP) or AEP plus Smart Health Coaching (SHC). All receive access to an online platform with exercise videos and wellness articles. After 4 weeks, participants are assessed for response; those not responding are re-randomized to receive live one-on-one or group exercise sessions via Zoom for the next 4 weeks. Following this, all participants enter a 24-week maintenance phase with access to prerecorded content only. Throughout the study, participants wear a tracker to monitor steps and activity, complete surveys at baseline, week 8, week 16, and week 32, and may have reminder calls to encourage survey completion. Data collected includes physical activity, health literacy, secondary health conditions, and activity limitations. Interviews are conducted after the adoption phases to gather further insights. The total participation lasts 32 weeks, with ongoing collection of exercise and website usage data to evaluate the adaptive interventions.
CONDITIONS
Brief Title
The Fit With Us Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Live with a permanent physical disability that limits mobility
- Be between 18 and 89 years old
- Have broadband internet access
- Be able to speak and read English
- Be able to attend coaching and training sessions during weekdays
You will not qualify if you...
- Have significant visual impairment preventing use of a computer screen for exercise
- Have been regularly exercising in the previous 3 months
- Unable to use arms and legs at all for exercise
- Considered unsafe to exercise
- Currently pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - Up to 4 weeks before intervention start
Participants provide consent, complete baseline surveys, receive and set up exercise tracking devices, and get oriented with the online platform.
1 to 2 remote sessions including welcome and orientation calls
Duration - Weeks 1 to 4
Participants engage in pre-recorded asynchronous exercise content. Those in the health coaching group may receive coaching calls. Participants complete a questionnaire at the end of this phase to assess response.
Weekly access to new exercise videos and health articles; up to 12 health coaching calls for some participants
Duration - Weeks 5 to 8
Responders continue with their assigned program. Non-responders receive additional live 1-on-1 or group training sessions remotely via ZOOM, up to 3 times per week.
Live training sessions up to 3 times per week for non-responders; continued access to exercise content for all
Duration - Weeks 9 to 32
Participants have open access to the exercise platform and continue using asynchronous content for maintenance of physical activity.
Ongoing remote access with occasional reminder calls to complete surveys
Duration - Throughout and at end of 32 weeks
Participants complete survey packets and semi-structured interviews at various points to evaluate progress and outcomes.
Survey completions at baseline, week 8, week 16, and week 32; semi-structured interview after week 8
Trial Site Locations
Total: 1 location
1
Wellness, Health and Research Facility
Birmingham, Alabama, United States, 35209
Actively Recruiting
Research Team
M
Mohanraj Thirumalai, PhD
S
Sangeetha Mohanraj, MS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
6
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