Actively Recruiting
Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)
Led by Baylor Research Institute · Updated on 2026-01-21
94
Participants Needed
1
Research Sites
264 weeks
Total Duration
On this page
Sponsors
B
Baylor Research Institute
Lead Sponsor
N
National Institute on Disability, Independent Living, and Rehabilitation Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
Investigators will conduct a randomized controlled trial (RCT) to assess intervention efficacy of telehealth delivery of the GLB-CVA (tGLB-CVA) compared to a 6-month wait-list control (WLC) in partnership with a diverse group of patient partners and peer mentors.
CONDITIONS
Official Title
Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Body Mass Index 6525
- Any type of stroke
- Able to participate in physical activity
- At least 12 months since first stroke
- Have internet, phone, or computer access or willing to use one provided by the study
You will not qualify if you...
- Contraindications for physical activity
- Low cognitive function
- Currently residing in hospital, acute rehab, or skilled nursing facility
- Not fluent in English
- Pre-existing eating disorder
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Baylor Scott & White Research Institute
Dallas, Texas, United States, 75204
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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