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Lifestyle, Eating, and Activity Patterns

Eating Frequency Prescription for a Behavioral Weigh Loss Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00944099
Acronym
LEAP
Enrollment
50
Registered
2009-07-23
Start date
2010-01-31
Completion date
2011-12-31
Last updated
2018-04-05

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

Conditions

Obesity, Overweight

Keywords

intervention studies, feeding behavior, eating frequency, weight loss, dietary intake

Brief summary

The purpose of this research is to test the effect of manipulating eating frequency on hunger and the reinforcing value of food in 50 overweight/obese adults participating in a 6-month behavioral weight loss intervention.

Detailed description

Previous observational and experimental research suggests that increased eating frequency is related to lower weight, body mass index (BMI)and body fatness. It is proposed that eating frequently during the day reduces overall energy consumed by preventing the development of excessive hunger. As elevated hunger increases the reinforcing value of food, and greater intake occurs when the reinforcing value of food increases, eating frequently during the day may be a dietary strategy that can aid with reducing energy intake and improving weight loss during a behavioral weight control program. Therefore, the purpose of this proposed research is to test the effect of manipulating eating frequency on hunger and the reinforcing value of food in 50 overweight/obese adults participating in a 6-month behavioral weight loss intervention. Participants will be randomized to 1 of 2 conditions: 1) a condition in which participants will be given an eating frequency prescription to eat every 2 to 3 hours (Grazing); or 2) a condition in which participants will be given an eating frequency prescription of eating 3 meals per day (Three Meals). Both conditions will receive an identical dietary prescription, a low-calorie (1200 to 1500 kcals/d), low-fat (≤ 30% kcals from fat) diet and an identical physical activity goal of 200 minutes of moderate-intense physical activity per week. Additionally, both conditions will receive an identical state-of-the-art, 6-month, behavioral weight loss program.

Interventions

both conditions will receive an identical dietary prescription, low-calorie and less than 30% calories from fat and an identical physical activity goal of 200 minutes of moderate-intense physical activity per week during a 6 month behavioral weight loss program

Sponsors

American Heart Association
CollaboratorOTHER
The University of Tennessee, Knoxville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 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 * report being unable to walk 1/4 mile without stopping * report major psychological disease or organic brain syndromes * report a diagnosis of type I or type II diabetes * are currently participating in a weight loss program, are taking weight loss medication, have had surgery for weight loss, or have lost \> 5% of their body weight in the past 6 months * are currently participating in a program that manipulates their eating habits * intent to move outside of the East Tennessee area within the time frame of the intervention * are pregnant, lactating, less than 6 months post-partum, or plan to become pregnant during the time frame of the intervention * are unwilling to attend group intervention meetings, assessments, or complete a food diary for the duration of the study

Design outcomes

Primary

MeasureTime frame
eating occasions per day0, 3, and 6 months
hunger and reinforcing value of food0, 3, and 6 months

Secondary

MeasureTime frame
energy and percent calories from fat intake0, 3, and 6 months
body weight, percent body fat, percent fat free mass0, 3, and 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026