20 Participants NeededMy employer runs this trial

Exercise Program for Diabetes and Mild Cognitive Impairment

LD
Overseen ByLiza Durgens
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of 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.

Who Is on the Research Team?

MS

Mandeep Sandhu, PhD, PT

Principal Investigator

University of Texas Medial Branch

Are You a Good Fit for This Trial?

Inclusion Criteria

4. Medication Stability: Stable medication regimen for at least 3 months
I have had type 2 diabetes for at least 5 years.
3. Cognitive Status: Mild cognitive impairment as defined by Petersen criteria and confirmed by Montreal Cognitive Assessment (MoCA) scores of 18-25
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants complete a 12-week progressive exercise program with 50-minute sessions three times per week, transitioning from supervised to unsupervised sessions

12 weeks
Weekly check-ins, final assessment at Week 13

Follow-up

Participants are monitored for changes in physical function, cognitive function, and glycemic control

1 week
Final assessment at Week 13

What Are the Treatments Tested in This Trial?

Interventions

  • Progressive Exercise Program

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Exercise ProgramExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

The University of Texas Medical Branch, Galveston

Lead Sponsor

Trials
263
Recruited
55,400+