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Clinical Trials/NCT01682317
NCT01682317
Active, not recruiting
Not Applicable

Healthy Eating Patterns During a Lifestyle Intervention

The University of Tennessee, Knoxville1 site in 1 country30 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
The University of Tennessee, Knoxville
Enrollment
30
Locations
1
Primary Endpoint
Diet
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to address the gap in knowledge regarding the relationship between eating frequency and weight loss.

Detailed Description

Little intervention research has been conducted to examine the influence of eating frequency (EF) on weight loss. It has been hypothesized an increased EF improves appetite control, assisting with better regulation of energy intake, thus decreasing body mass index. Unfortunately, outcomes have not shown greater appetite control with increased EF. Instead, trends favor a lower EF reducing energy intake thereby producing greater weight loss than a higher eating frequency. Thus, a lower eating frequency may lower energy intake via behavioral mechanisms. At thit time no research has examined the behavioral mechanisms that may mediate the relationship between a lower eating frequency and superior adherence to an energy-restricted diet.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
December 31, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
The University of Tennessee, Knoxville
Responsible Party
Principal Investigator
Principal Investigator

Hollie Raynor

Professor

The University of Tennessee, Knoxville

Eligibility Criteria

Inclusion Criteria

  • age between 18 and 65 years
  • healthy overweight and obese men and women
  • body mass index (BMI) between 27 and 45 kg/m squared

Exclusion Criteria

  • report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR- Q)
  • report being unable to walk for 2 blocks (1/4 mile) without stopping
  • are currently participating in a weight loss program and/or taking weight loss medication or lost \> 5% of body weight during the past 6 months
  • diagnosed with type 1 or 2 diabetes
  • have had bariatric surgery or are planning to have bariatric surgery in the next 4 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

Outcomes

Primary Outcomes

Diet

Time Frame: 0 and 8 weeks

Diet (eating frequency, kilocalories, macronutrients)

Secondary Outcomes

  • Anthropometrics(0 and 8 weeks)
  • Binge Eating(0 and 8 weeks)
  • Physical Activity(0 and 8 weeks)
  • Ecological Momentary Assessment (EMA)(0 and 8 weeks)

Study Sites (1)

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