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Eat Well for Life: A Weight Loss Maintenance Study

Eat Well for Life: A Weight Loss Maintenance Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01849627
Enrollment
345
Registered
2013-05-08
Start date
2014-08-01
Completion date
2025-12-31
Last updated
2026-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

weight loss maintenance

Brief summary

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.

Detailed description

Obesity increases the risk of several health conditions. Weight loss of 5-10% of initial weight reduces the risk of several diseases. This degree of weight loss is achievable in behavioral obesity programs. However, about 33% of initial weight loss is regained within one year and very little weight loss is maintained within three to five years. Thus, new strategies improving long-term weight loss maintenance are needed. One dietary strategy that increases self-reported satiation and satiety is consuming a low energy density (ED) diet. A low-ED diet allows a greater weight of food relative to total energy to be consumed, which is the proposed mechanism for the enhanced self-reported satiation and satiety found with low-ED meals. Research has shown that when participants are served low-ED meals, while total weight of food consumed does not change, meal energy intake decreases. Importantly, when low-ED meals are consumed across several days, reduced energy intake continues to occur, showing no degree of energy intake compensation. To address the gaps regarding the relationship between dietary ED and weight loss maintenance, we propose to conduct a randomized controlled trial (RCT) examining the effect of a low-ED prescription and its proposed mechanisms on weight loss maintenance. The primary hypotheses are: 1. Low-ED will have less weight regain than Energy Balance at 22 months. a. Weight regain at 10, 16, and 22 months will be examined to determine if differences occur between conditions. 2. Low-ED will consume a lower ED diet, less energy and percent energy from fat, and greater grams from solid food and fiber than Energy Balance at 10, 16, and 22 months. The secondary hypotheses are: 3. Identify mechanisms (mediators) by which reducing ED improves long-term lower energy intake, thus: 1. Low-ED will self-report lower hunger and greater satiation and satiety during EMA than Energy Balance at 10, 16, and 22 months.

Interventions

BEHAVIORALLow-ED

This condition will be instructed to make food consumption decisions based solely upon the ED of a food. The goal of the ED condition will be to consume at least 10 foods ≤ 1.0 kcal/g (i.e., fruits and vegetables, broth based soups, non-fat yogurts, some legumes, egg substitutes, some white fish, etc.) and no more than 2 foods ≥ 3.0 kcal/g (i.e., crackers, chips, cookies, hard cheeses, hot dogs, salad dressings, etc.) per day.

BEHAVIORALEnergy Balance

Energy Balance will receive an individualized daily energy goal which will be their measured resting metabolic rate multiplied by a physical activity level (PAL) of 1.12 (men) or 1.14 (women) (low active).

Sponsors

The University of Tennessee, Knoxville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

* 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 being unable to walk for 2 blocks (1/4 mile) without stopping * Report major psychiatric diseases or organic brain syndromes. * 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 * 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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Anthropometrics from Baseline at 4, 10, 16, and 22 months0, 4, 10, 16, and 22 monthsHeight, weight, and BMI will be assessed.
Changes in diet from baseline at 4, 10, 16, and 22 months0, 4, 10, 16, and 22 monthsThree day food records will be used to assess energy, grams, energy density, macronutrients, fiber, and food group servings.

Secondary

MeasureTime frameDescription
Changes in hunger, satiation, and satiety from baseline at 4, 10, 16, and 22 months0, 4, 10, 16, and 22 monthsChanges in EMA measures on hunger, satiation, and satiety will be assessed.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORHollie A Raynor, PhD, RD, LDN

University of Tennessee

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026