Home › Mild Cognitive Impairment › NCT05858008
Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
Recruiting
Who can join
Ages 45 to 95 · Women
Full eligibility criteria
Inclusion Criteria: * Postmenopausal Women * Age 45-95 * Diagnosis of mild cognitive impairment Exclusion Criteria: * Individuals prone to hypoglycemia * Liver disease * Taking medications that affect eating behaviors * Alcohol consumption of \>2 drinks per day * Significant circadian disruption * Having care-taking responsibilities that significantly affect sleep * Shift work or irregular lifestyle * Diagnosed clinical eating disorder * Participating in a formal weight loss program
About the study
This study will investigate the feasibility of implementing a time-restricted eating intervention in females with mild cognitive impairment. Targeted therapeutic interventions that improve cognitive impairment and delay onset of ADRD are particularly important for females, who have twice the lifetime risk of developing AD, compared to males.
What is being tested
- Time-restricted eating (behavioral)
Sponsor: Julie Pendergast · Participants: 15 · Started: Apr 1, 2024
Contact the study team
- Matt Thomas, PhD · Phone: (859) 218-6770
- Julie S Pendergast, PhD · Phone: (859) 218-6770
Official record on ClinicalTrials.gov — NCT05858008
Locations in the U.S.
| Kentucky | University of Kentucky, Lexington |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.