Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)
Recruiting
Efficacy of an Evidence-based Telehealth-delivered Weight-loss Intervention to Enhance Access and Reach Underserved Groups After Stroke
Who can join
Ages 18 to 85 · All sexes
Full 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
About the study
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.
What is being tested
- Group Lifestyle Balance for People Post Stroke (GLB-CVA) (behavioral)
Sponsor: Baylor Research Institute · Participants: 94 · Started: Dec 7, 2024
Contact the study team
Official record on ClinicalTrials.gov — NCT06569121
Locations in the U.S.
| Texas | Baylor Scott & White Research Institute, Dallas |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.