Ear Barotrauma Clinical Trials

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Feasibility and Adherence to a Technology-assisted Home-based Strength Training Program in Adults With Type 2 Diabetes Mellitus and Mild Cognitive Impairment

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a single-arm feasibility study employing a pre-post design with a 12-week intervention period. The study utilizes a telehealth-assisted home-based resistance exercise program, with a structured progression from supervised to unsupervised sessions over 12 weeks.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Maximum Age: 80
Healthy Volunteers: f
View:

• Age: 55-80 years

• Diabetes: Diagnosed T2DM with ≥5 years duration

• Cognitive Status: Mild cognitive impairment as defined by Petersen criteria and confirmed by Montreal Cognitive Assessment (MoCA) scores of 18-25

• Medication Stability: Stable medication regimen for at least 3 months

• Physical Capability: Physically capable of participating in moderate-intensity exercise (physician clearance required)

• Support System: Having a caregiver or support person willing to assist with technology use if needed

Locations
United States
Texas
University of Texas Medical Branch, Galveston
RECRUITING
Galveston
Contact Information
Primary
Liza Durgens
lidurgen@utmb.edu
(409)772-1011
Time Frame
Start Date: 2026-03
Estimated Completion Date: 2027-03
Participants
Target number of participants: 20
Treatments
Experimental: Exercise Program
Participants will complete a 12-week progressive exercise program with 50-minute sessions three times per week, including warm-up, resistance training, and cool-down. Supervision transitions from primarily in-person (Weeks 1-2) to mixed (Weeks 5-8) and mostly unsupervised with virtual support (Weeks 9-12). Weekly check-ins are provided, and a final assessment occurs at Week 13.
Related Therapeutic Areas
Type 2 Diabetes (T2D)
Ear Barotrauma
Sponsors
Leads: The University of Texas Medical Branch, Galveston

This content was sourced from clinicaltrials.gov

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