Feasibility and Adherence to a Technology-assisted Home-based Strength Training Program in Adults… (NCT07416799) | Clinical Trial Compass
RecruitingNot Applicable
Feasibility and Adherence to a Technology-assisted Home-based Strength Training Program in Adults With Type 2 Diabetes Mellitus and Mild Cognitive Impairment
United States20 participantsStarted 2026-03
Plain-language 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.
Who can participate
Age range55 Years – 80 Years
SexALL
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Inclusion criteria
✓. 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
Exclusion criteria
✕. Diagnosis of movement disorders such as multiple sclerosis, parkinson's disease
✕. Diagnosis of Alzheimer's disease,
✕. Current diagnosis of severe depression, major psychiatric conditions such as bipolar disorder, psychosis, schizophrenia, or alcoholism that could affect the ability to understand and/or cooperate fully with the protocol.
✕. Significant cerebral vascular disease
✕. Concomitant medications with significant cholinergic or anticholinergic effects or adverse effects on cognition, including antipsychotics, tricyclic antidepressants, anticonvulsants, sedative/hypnotics, anxiolytics, glucocorticoids (chronic or frequent intermittent),
What they're measuring
1
Feasibility of Technology-Assisted Home-Based Exercise Program
Timeframe: Week 13 (end of intervention and final assessment)
2
Acceptability of Technology-Assisted Home-Based Exercise Program
Timeframe: Week 13 (end of intervention and final assessment)
Trial details
NCT IDNCT07416799
SponsorThe University of Texas Medical Branch, Galveston