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NCT05699772
Expanding Delivery of an Evidence-based Weight-loss Intervention to Enhance Access and Reach Underserved Groups After TBI
Conditions: Traumatic Brain Injury
Sex: All
Ages: 18 Years – 64 Years
Phase: NA
Enrollment: 88
Sponsor: Baylor Research Institute
Location: United States
Summary
The goal of this clinical trial is to extend the accessibility of the Diabetes Prevention Program Group Lifestyle Balance (DPP-GLB) modified for people with TBI (GLB-TBI) to reduce health inequities and reach a broad and diverse sample.To increase the accessibility and reach of the GLB-TBI we will conduct a randomized control trial (RCT) to assess intervention efficacy of telehealth delivery of the GLB-TBI (tGLB-TBI).
Results will provide a scalable telehealth weight-loss program that clinicians and community workers across the country can use to help people with TBI lose weight and improve health.
Eligibility Criteria
Inclusion Criteria:18-64 years of ageGreater than or equal to 6 months post traumatic brain injury (TBI)Moderate to severe TBI at time of injuryBody Mass Index greater than or equal to 25Able to participate in physical activityWilling to use a tablet/computer/smartphone (either personal device or one provided by the research team)Exclusion Criteria:Contraindications to physical activity (e.g., uncontrolled hypertension, unstable angina, severe joint disease, uncontrolled vertigo/dizziness)Not fluent in the English languageLow cognitive functionResiding in a hospital, acute rehabilitation facility, or skilled nursing facilityDiagnosed with or taking medications for Type 2 diabetesSelf-reported pregnancyPre-existing diagnosis of an eating disorder
Source: ClinicalTrials.gov (NCT05699772). StuddyBuddy aggregates publicly available trial information.