← Eichor
Study identifier: NCT07481513 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Impact of Intermittent Fasting on the Mental Health of Perimenopausal Women

Condition: Mental Health · Perimenopause · Intermittent Fasting  ·  Sponsor: American University of Beirut Medical Center

PhaseNA
Planned participants140
Who can joinFemale, 45 Years to 55 Years
Healthy volunteersYes

About this study

This study will explore how intermittent fasting (specifically the 16/8 method) affects the mental health of women who are in the perimenopause stage. This life stage often brings hormonal changes that can impact emotional and physical well-being. The study will include 98 women aged 45-55, who will be randomly divided into two groups. The study will compare the mental health outcomes of those who follow intermittent fasting with those who do not, using independent t-tests to analyze the results. The goal is to better understand if intermittent fasting can help improve mental health during perimenopause.

This description comes directly from the study's public registry record.

Talk to the study team

Nadia T Dandan, PsyD  ·  +9613795428  ·  nd55@aub.edu.lb

Sara El Hajj, BA  ·  +96181727230  ·  se148@aub.edu.lb

Always discuss trial participation with your own doctor first.

Locations (1)

American University of Beirut Medical CenterBeirut, LebanonRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07481513