Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06491537

Time-restricted Eating for Postpartum Weight Loss

Led by University of Alabama at Birmingham · Updated on 2025-06-12

60

Participants Needed

1

Research Sites

193 weeks

Total Duration

On this page

Sponsors

U

University of Alabama at Birmingham

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is being done to assess the feasibility and acceptability of a time-restricted eating intervention among postpartum women with overweight/obesity.

CONDITIONS

Official Title

Time-restricted Eating for Postpartum Weight Loss

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Experienced a healthy singleton pregnancy
  • 6-16 weeks postpartum at enrollment
  • Body mass index 25 at enrollment
  • Willing to consent
Not Eligible

You will not qualify if you...

  • Self-reported major health condition such as renal disease, cancer, or Type 1 or Type 2 diabetes
  • Current treatment for severe psychiatric disorder such as schizophrenia
  • Self-reported diagnosis of anorexia or bulimia
  • Current use of medication expected to significantly impact body weight
  • Current substance abuse
  • Participation in another dietary and/or weight management intervention postpartum
  • Performing overnight shiftwork more than once per week
  • Regularly fasting 14 hours or more per day or completing twelve or more 24-hour fasts within the past year
  • Unable to understand and communicate in English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294

Actively Recruiting

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Research Team

C

Camille S Worthington, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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