RECRUITING

Early vs. Late Time-Restricted Eating in Adolescents With Obesity (EL TREA)

Conditions

Pediatric Obesity Time Restricted Feeding Time Restricted Eating Obesity Intermitted-fasting Time Limited Eating

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Determine the effectiveness of how limiting the time you eat within an early or late eating window and fasting for remainder of the day will impact weight loss and body mass index (BMI).

Official Title

Early vs. Late Time-Restricted Eating in Adolescents With Obesity (EL TREA)

Quick Facts

Study Start:2023-03-27

Study Completion:2027-01-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05740254

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 21 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT

Inclusion Criteria	Exclusion Criteria
* 12-21 years with obesity (BMI\>95th percentile) * participant must be willing and able to adhere to the assessments, visit schedules, and eating/fasting periods * baseline eating window greater than 12 hours.	* diagnosis of Prader-Willi Syndrome, brain tumor, or diabetes serious intellectual disability * previous diagnosis or subthreshold symptoms of an eating disorder (anorexia nervosa, bulimia nervosa, binge-eating disorder) * parent/guardian-reported physical, mental of other inability to participate in the assessments * previous bariatric surgery * current participation in other interventional weight loss studies.

Inclusion Criteria

Exclusion Criteria

* 12-21 years with obesity (BMI\>95th percentile)
* participant must be willing and able to adhere to the assessments, visit schedules, and eating/fasting periods
* baseline eating window greater than 12 hours.

* diagnosis of Prader-Willi Syndrome, brain tumor, or diabetes serious intellectual disability
* previous diagnosis or subthreshold symptoms of an eating disorder (anorexia nervosa, bulimia nervosa, binge-eating disorder)
* parent/guardian-reported physical, mental of other inability to participate in the assessments
* previous bariatric surgery
* current participation in other interventional weight loss studies.

Contacts and Locations

Study Contact

Alaina Vidmar, MD

CONTACT

323-361-4606

avidmar@chla.usc.edu

Harvey Peralta

CONTACT

hperalta@chla.usc.edu

Principal Investigator

Alaina Vidmar, MD

PRINCIPAL_INVESTIGATOR

Children's Hospital Los Angeles

Study Locations (Sites)

Children's Hospital Los Angeles

Los Angeles, California, 90027

United States

Collaborators and Investigators

Sponsor: Children's Hospital Los Angeles

Alaina Vidmar, MD, PRINCIPAL_INVESTIGATOR, Children's Hospital Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-03-27

Study Completion Date2027-01-01

Study Record Updates

Study Start Date2023-03-27

Study Completion Date2027-01-01

Terms related to this study

Keywords Provided by Researchers

Obesity
Intermitted-fasting
Time Limited Eating

Additional Relevant MeSH Terms

Pediatric Obesity
Time Restricted Feeding
Time Restricted Eating