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

RECRUITINGN/ASponsored by Baylor Research Institute
Actively Recruiting
PhaseN/A
SponsorBaylor Research Institute
Started2024-12-07
Est. completion2027-08-31
Eligibility
Age18 Years – 85 Years
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →

NCT06569121

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

Age: 18 Years – 85 YearsHealthy volunteers accepted
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

Conditions7

Heart DiseaseStrokeStroke (CVA) or TIAStroke, AcuteStroke, CardiovascularStroke/Brain AttackWeight Loss

Locations1 site

Baylor Scott & White Research Institute
Dallas, Texas, 75204
Stephanie Calhoun, BS214.228.5181Stephanie.Calhoun1@BSWHealth.org

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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