Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorBaylor Research Institute
About this trial
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
Qualifiers
Body Mass Index ≥25
All types of stroke
Able to Participate in Physical Activity
≥12 months post first stroke
Disqualifiers
Contraindications for physical activity
Low Cognitive Function
Residing in hospital, acute rehab, skilled nursing facility
Not fluent in the English language
Trial design
Treatments tested in this trial
- Group Lifestyle Balance for People Post Stroke (GLB-CVA)
Treatment groups
94 Participants
are divided into 2 treatment groupsSponsors and collaborators
Baylor Research Institute
Lead sponsor
National Institute on Disability, Independent Living, and Rehabilitation Research
Collaborator
Source ClinicalTrials.gov