MBC: Make Better Choices Study

Sponsor
Northwestern University (Other)
Overall Status
Completed
CT.gov ID
NCT00113672
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
204
1
4
70
2.9

Study Details

Study Description

Brief Summary

The purpose of this study is to examine the impact of diet and exercise on an individual's health.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Increase healthy activity and increase healthy eating
  • Behavioral: Decrease unhealthy activity and increase healthy eating
  • Behavioral: Increase physical activity and decrease unhealthy eating
  • Behavioral: Decrease sedentary activity and decrease unhealthy eating
N/A

Detailed Description

BACKGROUND:

The majority of adult Americans consume a high saturated fat diet, have a low fruit and vegetable (F/V) intake, and lead a sedentary lifestyle. This unhealthy lifestyle heightens their risk for cardiovascular disease and cancer. Improving diet and activity can reduce risk, but the best prescription to promote a healthier diet and a more active lifestyle remains unknown. This study will randomly assign participants to 4 groups, which will include all combinations of increasing healthy eating and activity and decreasing unhealthy eating and activity. The Familiarity Hypothesis predicts that the most familiar dieting prescription (decrease fat, increase physical activity) will maximize healthy behavior change. The Optimal Substitution Hypothesis, based on Behavioral Economic Theory, predicts that increasing F/V intake while decreasing sedentary behavior will surpass alternative methods by maximizing behavioral substitution of healthful eating and activity for unhealthful eating and activity. The Low Inhibitory Demand Hypothesis, based on Self-Control Theory, predicts that increasing F/Vs while increasing physical activity will be most successful because this prescription places the fewest demands on self-control resources.

DESIGN NARRATIVE:

The study will randomize 200 sedentary community-dwelling adults with a suboptimal diet to 1 of 4 groups including: 1) increase healthy eating and activity; 2) decrease unhealthy eating and activity; 3) increase healthy eating and decrease unhealthy activity; and 4) decrease unhealthy eating and increase healthy physical activity. Subjects will self-monitor diet, physical activity, and mood via PDAs during a 2-week baseline period, a 3-week prescription period (when payment is contingent upon changing eating and activity simultaneously to targeted standards), and a 4-month maintenance period. Targeted and collateral diet and activity changes will be measured by self report, accelerometer, and grocery receipts. Bogus pipeline urinary testing will encourage adherence. Laboratory testing will measure behavioral choices, craving, and attentional allocation to restricted foods and activities in a permissive context in order to shed light on behavioral and psychological processes that mediate healthy lifestyle change. Findings will help to fill an important gap in clinical knowledge about how to optimize healthy simultaneous change in diet and activity among adults.

Study Design

Study Type:
Interventional
Actual Enrollment :
204 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Multiple Behavior Change in Diet and Activity
Study Start Date :
Aug 1, 2004
Actual Primary Completion Date :
Jun 1, 2010
Actual Study Completion Date :
Jun 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: A

Increase healthy eating and increase healthy activity

Behavioral: Increase healthy activity and increase healthy eating
Increase participants to 60 minutes of activity per day and 5 fruits and vegetables per day over a 3 week prescription phase

Experimental: B

Increase healthy eating and decrease unhealthy activity

Behavioral: Decrease unhealthy activity and increase healthy eating
Decrease sedentary activity by 90 minutes per day and increase fruits and vegetables to 5 servings per day over the course of a 3 week prescription phase

Experimental: C

Decrease unhealthy eating and increase healthy activity

Behavioral: Increase physical activity and decrease unhealthy eating
Increase physical activity up to 60 minutes per day and decrease saturated fat to an average of 8% per day over the course of a 3 week prescription phase

Experimental: D

Decrease unhealthy activity and decrease unhealthy eating

Behavioral: Decrease sedentary activity and decrease unhealthy eating
Decrease sedentary activity by 90 minutes per day and decrease saturated fat to and average of 8% per day over the course of a 3 week prescription phase

Outcome Measures

Primary Outcome Measures

  1. Daily diet and activity (measured at Week 1 and 3, and Month 1, 2, 3, 4, 5, and 6) [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Sedentary community dwelling adults with a suboptimal diet

  • Motivated to make changes in diet and activity level

Exclusion Criteria:
  • Few exclusion criteria will be implemented in order to enhance generalizability

  • For safety, participants with unstable medical conditions (uncontrolled hypertension, diabetes, recent myocardial infarction) will be excluded. Those with stable medical conditions will require physician approval to participate but will not be excluded because the prescribed changes in diet and activity match healthy, attainable guidelines for all Americans.

  • Cannot read the study questionnaires

  • Committed to following an incompatible dietary regimen

  • Pregnant, trying to get pregnant, or breastfeeding

  • People with anorexia, bulimia, or report active suicidal ideation will not be enrolled because they might practice overly severe dietary restrictions

  • Binge eating disorder

  • Current substance abuse or dependence, other than nicotine dependence will be excluded because of concern about their ability to maintain accurate records of intake and activity. Smokers will be accepted and during recreational laboratory sessions will be able to smoke cigarettes in an adjoining room that is used as a smoking laboratory.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northwestern University Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University
  • National Heart, Lung, and Blood Institute (NHLBI)

Investigators

  • Principal Investigator: Bonnie Spring, PhD, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Bonnie Spring, Professor, Northwestern University
ClinicalTrials.gov Identifier:
NCT00113672
Other Study ID Numbers:
  • 182
  • R01HL075451
First Posted:
Jun 10, 2005
Last Update Posted:
Apr 4, 2013
Last Verified:
Apr 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 4, 2013