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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55-80
SponsorThe University of Texas Medical Branch, Galveston

About this trial

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 criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Progressive Exercise Program (12 Weeks)

Treatment groups

20 Participants
are divided into 1 treatment group