ClinicalTrials.Veeva

Menu

Promoting Long-term Behavior Change to Reduce CVD Risk

Stanford University logo

Stanford University

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Behavioral lifestyle/weight-loss intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00227006
R29HL060154 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Once intervention class or staff contact is removed, obese adults participating in behavioral weight-loss programs often give up healthy eating habits and regain weight. We examined whether taste-based goal setting, which minimizes perceived deprivation by promoting taste and moderation, would sustain long-term reductions in saturated fat and body mass index (BMI).

Full description

Once intervention class or staff contact is removed, obese adults participating in behavioral weight-loss programs often give up healthy eating habits and regain weight. We examined whether taste-based goal setting, which minimizes perceived deprivation by promoting taste and moderation, would sustain long-term reductions in saturated fat and body mass index (BMI). Participants were randomized to Taste-Based Choices (taste-based goal setting + a standard 6-month behavioral weight-loss intervention), Smart Consumers (a standard 6-month intervention alone) or Community Access (access to commercial/community-based behavioral weight-loss programs) and followed over 18 months. To test our hypotheses, we examined a set of orthogonal contrasts (TBC and SC vs. CA; TBC vs. SC) on reductions in saturated fat (Block FFQ) and clinic-measured BMI.

Enrollment

163 patients

Sex

All

Ages

25+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:- Body mass index between 27-37

  • Physically inactive
  • Able to participate in physical activity
  • Percentage of daily calories from total fat 30% or more
  • Free of diagnosed heart disease
  • Stable on medications for 3 months or more Exclusion Criteria:- Diabetic
  • Dysphoric (Beck Depression Inventory score greater than 18)
  • Binge eating or bulimic (Eating Disorder Diagnostic Scale)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

163 participants in 3 patient groups

Taste-Based Goal Setting
Experimental group
Description:
6-month intervention (14 lifestyle counseling classes)
Treatment:
Behavioral: Behavioral lifestyle/weight-loss intervention
Smart Consumers
Active Comparator group
Description:
6-month intervention (14 lifestyle counseling classes)
Treatment:
Behavioral: Behavioral lifestyle/weight-loss intervention
Community Access
Active Comparator group
Description:
Can enroll in behavioral treatment programs available in the community that do not include medication or very-low calorie diets
Treatment:
Behavioral: Behavioral lifestyle/weight-loss intervention

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems