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NCT01849627Completed

Eat Well for Life: A Weight Loss Maintenance Study

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

A study to investigate the effect of a low-ED prescription (consume ≥10 foods ≤ 1.0 kcal/g and ≤ 2 foods ≥ 3.0 kcal/g per day) versus an energy balance prescription (consume a daily energy intake at estimated energy needs for maintenance) on weight loss maintenance.

Status (registry)
Completed
Study type
Interventional
Enrollment
345 (estimated)
First submitted
30 Apr 2013
Start date
Aug 2014
Primary completion date
31 Dec 2024
Lead sponsor
The University of Tennessee, Knoxville
Diseases
Obesity
NCT number
NCT01849627

What you commit to

  • Study type: Interventional
  • Planned participants: 345
  • From Aug 2014 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Are 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
  • Have had bariatric surgery for weight loss or are planning to have bariatric surgery in the next 22 months

Other illness

  • Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire
  • 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 major psychiatric diseases or organic brain syndromes.

Other

  • Report being unable to walk for 2 blocks (1/4 mile) without stopping
  • Intend to move outside of the metropolitan area within the time frame of the investigation
  • Are pregnant, lactating, \< 6 months post-partum, or plan to become pregnant during the investigation
  • Report not being able to consume meal replacements
    • To participate in the weight loss maintenance phase, participants will need to lose equal to or greater than 8% of their body weight from the baseline measure at the conclusion of the 4-month weight loss phase.

Who the study is looking for

  • Age between 18 and 70 years
  • Body mass index (BMI) between 27 and 45 kg/m2

Age in the registry: 18 years to 70 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Tennessee
Coordinator of this site? Confirm its status
KnoxvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.