Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
Recruiting
N/A
Interventional Study
Mild Cognitive Impairment
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 45 – 95
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 15 (estimated)
- Sponsor
- Julie Pendergast · Other
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About This Trial
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.
Trial Locations
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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
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Contacts