RecruitingNot ApplicableNCT06569121

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

Efficacy of an Evidence-based Telehealth-delivered Weight-loss Intervention to Enhance Access and Reach Underserved Groups After Stroke


Sponsor

Baylor Research Institute

Enrollment

94 participants

Start Date

Dec 7, 2024

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a behavioral approach called Group Lifestyle Balance for People Post Stroke (GLB-CVA) for people with stroke, stroke (cva) or tia, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

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

12-month healthy lifestyle and weight loss program modified from the Diabetes Prevention Program Group Lifestyle Balance (DPP-GLB)


Locations(1)

Baylor Scott & White Research Institute

Dallas, Texas, United States

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NCT06569121


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