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NCT06491537 · ClinicalTrials.gov registry record · NA
Time-restricted Eating for Postpartum Weight Loss
A NA study of Overweight and Obesity and Postpartum Weight Retention, sponsored by University of Alabama at Birmingham.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT06491537: Recruiting NA study of Overweight and Obesity and Postpartum Weight Retention, sponsored by University of Alabama at Birmingham.
NCT06491537 is a NA study of Overweight and Obesity and Postpartum Weight Retention that is actively recruiting participants, run by University of Alabama at Birmingham. The registered enrollment target is 60 participants, below the 228-participant average among 115 other Overweight and Obesity trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06491537, a NA study of Overweight and Obesity and Postpartum Weight Retention, is actively recruiting participants, sponsored by University of Alabama at Birmingham.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is being done to assess the feasibility and acceptability of a time-restricted eating intervention among postpartum women with overweight/obesity.
Primary Outcome
Percentage of eligible subjects who agreed to participate out of those who were screened.
Conditions Studied
Interventions
- BEHAVIORAL Control
- BEHAVIORAL Early Time-Restricted Eating (eTRE)
Study Locations (1)
Alabama
- University of Alabama at Birmingham - Birmingham
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2025-05-22 |
| Est. Completion | 2029-02-01 |
| Phase | NA |
What NCT06491537 shows while recruiting
NCT06491537 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 228-participant average among 115 other Overweight and Obesity trials with a reported enrollment target (74% lower).
The record links to 2 conditions, with Overweight and Obesity appearing as the primary indexed condition, and to 2 interventions - of which Control is the first listed.
NCT06491537 reports a single indexed study location in Alabama.
Frequently Asked Questions
What is clinical trial NCT06491537 about?
NCT06491537 is a clinical study titled "Time-restricted Eating for Postpartum Weight Loss". This study is being done to assess the feasibility and acceptability of a time-restricted eating intervention among postpartum women with overweight/obesity.
What is the current status of trial NCT06491537?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2025-05-22. Estimated completion is 2029-02-01.
What conditions does trial NCT06491537 study?
This clinical trial studies the following conditions: Overweight and Obesity, Postpartum Weight Retention.
What interventions are being tested in trial NCT06491537?
The interventions under investigation include: Control (BEHAVIORAL), Early Time-Restricted Eating (eTRE) (BEHAVIORAL).
Who is sponsoring clinical trial NCT06491537?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06491537 being conducted?
This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06491537's enrollment target sits among peer trials
60 79th of 115 higher than 34 of 115 other Overweight and Obesity trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Overweight and Obesity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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