Make Better Choices Study

NCT ID: NCT00113672

Last Updated: 2013-04-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 204 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-08-31
• Study Completion Date: 2010-06-30

Brief Summary

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

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.

Conditions

Cardiovascular Diseases; Heart Diseases

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

A

Increase healthy eating and increase healthy activity

Group Type: EXPERIMENTAL

Increase healthy activity and increase healthy eating

Intervention Type: BEHAVIORAL

Increase participants to 60 minutes of activity per day and 5 fruits and vegetables per day over a 3 week prescription phase

B

Increase healthy eating and decrease unhealthy activity

Group Type: EXPERIMENTAL

Decrease unhealthy activity and increase healthy eating

Intervention Type: BEHAVIORAL

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

C

Decrease unhealthy eating and increase healthy activity

Group Type: EXPERIMENTAL

Increase physical activity and decrease unhealthy eating

Intervention Type: BEHAVIORAL

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

D

Decrease unhealthy activity and decrease unhealthy eating

Group Type: EXPERIMENTAL

Decrease sedentary activity and decrease unhealthy eating

Intervention Type: BEHAVIORAL

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

Interventions

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

Intervention Type: 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

Intervention Type: 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

Intervention Type: 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

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Sedentary community dwelling adults with a suboptimal diet
• Motivated to make changes in diet and activity level

Exclusion Criteria

• 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.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role: collaborator

Northwestern University

OTHER

Sponsor Role: lead

Responsible Party

Bonnie Spring

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Bonnie Spring, PhD

Role: PRINCIPAL_INVESTIGATOR

Northwestern University

Locations

Northwestern University

Chicago, Illinois, United States

Countries

United States

References

Welch WA, Groth CP, Phillips SM, Spring B, Siddique J. Comparing Accelerometer and Self-Reported Treatment Effects in a Technology-Supported Physical Activity Intervention. Health Educ Behav. 2021 Feb;48(1):34-41. doi: 10.1177/1090198120971194. Epub 2020 Nov 13.

Reference Type: DERIVED

PMID: 33185131 (View on PubMed)

Spring B, Schneider K, McFadden HG, Vaughn J, Kozak AT, Smith M, Moller AC, Epstein L, Russell SW, DeMott A, Hedeker D. Make Better Choices (MBC): study design of a randomized controlled trial testing optimal technology-supported change in multiple diet and physical activity risk behaviors. BMC Public Health. 2010 Sep 29;10:586. doi: 10.1186/1471-2458-10-586.

Reference Type: DERIVED

PMID: 20920275 (View on PubMed)

Other Identifiers

R01HL075451

Identifier Type: NIH

Identifier Source: secondary_id

View Link

182

Identifier Type: -

Identifier Source: org_study_id