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Recruiting NCT06569121
Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)
Trial Parameters
Condition Stroke, Acute
Sponsor Baylor Research Institute
Study Type INTERVENTIONAL
Phase N/A
Enrollment 94
Sex ALL
Min Age 18 Years
Max Age 85 Years
Start Date 2024-12-07
Completion 2027-08-31
Interventions
Group Lifestyle Balance for People Post Stroke (GLB-CVA)
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * Body Mass Index ≥25 * All types of stroke * Able to Participate in Physical Activity * ≥12 months post first stroke * Have internet, phone, or computer access, or be willing to use one provided by the study team Exclusion Criteria: * Contraindications for physical activity * Low Cognitive Function * Residing in hospital, acute rehab, skilled nursing facility * Not fluent in the English language * Pre-existing eating disorder * Pregnancy
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