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Search / Trial NCT06455995

Daily Eating Patterns for Total Health Study

Launched by THE UNIVERSITY OF TENNESSEE, KNOXVILLE · Jun 6, 2024

Trial Information

Current as of August 20, 2025

Recruiting

Keywords

ClinConnect Summary

The Daily Eating Patterns for Total Health Study is a clinical trial aimed at understanding how the timing of meals can affect long-term weight loss, particularly in people with obesity. The researchers want to see if eating most calories in the morning or evening makes a difference in how much weight participants lose over a year. They will also look at how these eating patterns affect sleep, appetite, and overall eating habits.

To participate, individuals need to have a body mass index (BMI) between 27 and 45. Participants will follow a reduced-calorie, low-fat diet, try to be physically active for at least 200 minutes a week, and receive support through a behavioral program. It's important to note that certain health conditions or medications that affect eating or sleep might prevent someone from joining the study. Participants will be recruited from a wide age range, and everyone will have the chance to contribute to valuable research on weight management.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Body mass index (BMI) between 27 and 45 kg/m2.
  • Exclusion Criteria:
  • Report not regularly (\>/= 5 days/wk) consuming energy (\>/= 100 kcal) prior to 12 pm, and not being able to consume energy every day (\>/= 50 kcal) within one hour of awakening.
  • Report taking sleep medication or not regularly (\>/= 5 nights/wk) getting at least 6 hrs of total sleep.
  • Report being a shift workers/alternative shift workers that work outside of 7 am and 7 pm.
  • Report being diagnosed with type 1, or type 2 diabetes and taking medication that requires eating to occur at certain time periods.
  • Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals reporting joint problems, prescription medication usage, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.
  • Report being unable to walk for 2 blocks (1/4 mile) without stopping.
  • Report major psychiatric diseases or organic brain syndromes.
  • Report currently participating in a weight loss program and/or taking weight loss or appetite regulation medication or lost \>/= 5% of body weight during the past 6 months.
  • Report having bariatric surgery for weight loss/planning to have bariatric surgery in the next 12 months.
  • Report being pregnant, lactating, \< 6 months post-partum or plan to become pregnant (next 12 months).
  • Report planning to move outside of the metropolitan area within the time frame of the investigation.
  • Do not have daily access to PC with internet or smartphones (needed for self-monitoring).

About The University Of Tennessee, Knoxville

The University of Tennessee, Knoxville, is a prestigious public research institution dedicated to advancing knowledge and innovation in various fields, including health sciences. With a strong emphasis on interdisciplinary collaboration, the university conducts cutting-edge clinical trials aimed at improving patient outcomes and contributing to the scientific community. Its state-of-the-art facilities and commitment to ethical research practices ensure rigorous study design and execution, positioning the university as a leader in clinical research and a valuable partner in the quest for medical advancements.

Locations

Knoxville, Tennessee, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported