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

Recruiting now · Not applicable

Conditions studied: Stroke, Acute, Stroke, Stroke, Cardiovascular, Stroke (CVA) or TIA, Stroke/Brain Attack

In brief

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.

Key facts

Study ID

NCT06569121

Run by

Baylor Research Institute

People needed

94

Starts

2024-12-07

Expected to finish

2029-12-31

Last updated by the study team

2026-01-21

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Baylor Scott & White Research Institute — Dallas, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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