RecruitingNot Applicable

Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)

United States94 participantsStarted 2024-12-07

Plain-language 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.

Who can participate

Age range18 Years – 85 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Body Weight

Timeframe: Baseline, 3, 6, 9, 12, 18 month

Trial details

NCT IDNCT06569121

SponsorBaylor Research Institute

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-08-31

View on ClinicalTrials.gov More Stroke, Acute trials