Actively Recruiting

Phase Not Applicable
Age: 25Years - 60Years
All Genders
NCT06455995

Daily Eating Patterns for Total Health Study

Led by The University of Tennessee, Knoxville · Updated on 2024-11-27

174

Participants Needed

1

Research Sites

228 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this randomized controlled trial is to learn how the time of day when calories are eaten affects weight loss in the long-term (12 months). The main aims are to learn: 1. The influence of time-based energy intake goals on longer-term weight loss. 2. The influence of time-based energy intake goals on eating temporal patterns, sleep regularity, and appetite regulation. Researchers will compare whether goals to eat most of a person's calories in the morning or evening work to treat obesity. Participants will: 1. Eat a reduced-calorie, low-fat diet (some participants will have goals to eat their calories at certain times of day based on their group) 2. Be physically active at least 200 minutes 3. Receive a cognitive behavioral intervention

CONDITIONS

Official Title

Daily Eating Patterns for Total Health Study

Who Can Participate

Age: 25Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Body mass index (BMI) between 27 and 45 kg/m2.
Not Eligible

You will not qualify if you...

  • Not regularly consuming energy (\u2265 100 kcal) before 12 pm at least 5 days per week, or not able to consume energy (\u2265 50 kcal) daily within one hour of waking.
  • Taking sleep medication or not regularly getting at least 6 hours of total sleep at least 5 nights per week.
  • Working shift or alternative shifts outside 7 am to 7 pm.
  • Diagnosed with type 1 or type 2 diabetes and taking medication requiring eating at specific times.
  • Having a heart condition, chest pain during activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire.
  • Joint problems, prescription medication use, or medical conditions limiting exercise without physician consent.
  • Unable to walk 2 blocks (1/4 mile) without stopping.
  • Major psychiatric diseases or organic brain syndromes.
  • Currently participating in a weight loss program, taking weight loss or appetite-regulating medication, or lost 5% or more of body weight in past 6 months.
  • Had or planning bariatric surgery within the next 12 months.
  • Pregnant, lactating, less than 6 months postpartum, or planning pregnancy within 12 months.
  • Planning to move outside the metropolitan area during the study period.
  • No daily access to a PC with internet or smartphones needed for self-monitoring.

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

Healthy Eating and Activity Laboratory

Knoxville, Tennessee, United States, 37996

Actively Recruiting

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Research Team

H

Hollie A Raynor, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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