Actively Recruiting
Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
Led by Julie Pendergast · Updated on 2025-12-29
15
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
Sponsors
J
Julie Pendergast
Lead Sponsor
N
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postmenopausal women
- Age between 45 and 95 years
- Diagnosis of mild cognitive impairment
You will not qualify if you...
- Individuals prone to hypoglycemia
- Liver disease
- Taking medications that affect eating behaviors
- Alcohol consumption of more than 2 drinks per day
- Significant circadian disruption
- Care-taking responsibilities that significantly affect sleep
- Shift work or irregular lifestyle
- Diagnosed clinical eating disorder
- Participating in a formal weight loss program
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Kentucky
Lexington, Kentucky, United States, 40536
Actively Recruiting
Research Team
M
Matt Thomas, PhD
CONTACT
J
Julie S Pendergast, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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