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

Study acronym: tGLB-CVA
StatusRecruiting
PhaseNot applicable
Started
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Record History

See every version on ClinicalTrials.gov ↗

  1. Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 16 of 21 entries
    • Site details revised
  2. Re-verified, no change to tracked fieldsv4
  3. Start date changed from estimate of Nov 1, 2024 to Dec 7, 2024
    • Eligibility criteria shortened, about 9 words
    • Secondary endpoints: details revised at 1 of 21 entries
    • Site contact updated
    v3
  4. Trial status: Not Yet Recruiting to Recruiting
    • Start date: Oct 1, 2024 to Nov 1, 2024
    • Site details revised
    v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Baylor Research Institute
117 trials monitored
See 10 trials at risk
Heart Disease
8,786 trials monitored
See 412 trials at risk
Stroke
3,531 trials monitored
See 153 trials at risk
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.
Trial Details
NCT Number NCT06569121
Lead Sponsor Baylor Research Institute
Collaborators: National Institute on Disability, Independent Living, and Rehabilitation Research
Conditions
(from sponsor)		 Stroke, Acute, Stroke, Stroke, Cardiovascular, Stroke (CVA) or TIA, Stroke/Brain Attack
Related terms Myocardial Infarction, Stroke
Enrollment 94 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov