NCT06569121NARecruiting

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

Baylor Research Institute

Start Date

12/7/2024

Completion Date

12/31/2029

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

Age Range: 18 years to 85 years

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

Interventions

BEHAVIORAL

Group Lifestyle Balance for People Post Stroke (GLB-CVA)

Interested in This Trial?

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Conditions

Stroke, AcuteStrokeStroke, CardiovascularStroke (CVA) or TIAStroke/Brain Attack

Locations

Baylor Scott & White Research Institute

Dallas, Texas 75204

United States