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

Description

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.

Conditions

Stroke, Acute, Stroke, Stroke, Cardiovascular, Stroke (CVA) or TIA, Stroke/Brain Attack

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Study Overview

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Study Details

Study overview

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.

Efficacy of an Evidence-based Telehealth-delivered Weight-loss Intervention to Enhance Access and Reach Underserved Groups After Stroke

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

Condition
Stroke, Acute
Intervention / Treatment

-

Contacts and Locations

Dallas

Baylor Scott & White Research Institute, Dallas, Texas, United States, 75204

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * Diagnosed with or taking medication for Type 2 diabetes
  • * 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

Ages Eligible for Study

18 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Baylor Research Institute,

Study Record Dates

2029-12-31