Status:

RECRUITING

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

Lead Sponsor:

Baylor Research Institute

Collaborating Sponsors:

National Institute on Disability, Independent Living, and Rehabilitation Research

Conditions:

Stroke, Acute

Stroke

Eligibility:

All Genders

18-85 years

Phase:

NA

Brief 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 partner...

Eligibility Criteria

Inclusion

  • 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

  • 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

Key Trial Info

Start Date :

December 7 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2029

Estimated Enrollment :

94 Patients enrolled

Trial Details

Trial ID

NCT06569121

Start Date

December 7 2024

End Date

December 31 2029

Last Update

January 27 2025

Active Locations (1)

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Baylor Scott & White Research Institute

Dallas, Texas, United States, 75204