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Behavioral Self-Regulation

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
The Miriam Hospital
ClinicalTrials.gov Identifier:
NCT00488228
First received: June 18, 2007
Last updated: April 12, 2012
Last verified: January 2008

June 18, 2007
April 12, 2012
April 2007
November 2007   (final data collection date for primary outcome measure)
weight change [ Time Frame: 10 weeks and 20 weeks ] [ Designated as safety issue: No ]
weight change [ Time Frame: 10 weeks and 20 weeks ]
Complete list of historical versions of study NCT00488228 on ClinicalTrials.gov Archive Site
eating disorder symptoms, physical activity, body image, mood symptoms, and self-efficacy about eating behavior [ Time Frame: 10 weeks and 20 weeks ] [ Designated as safety issue: No ]
eating disorder symptoms, physical activity, body image, moos symptoms, and self-efficacy about eating behavior [ Time Frame: 10 weeks and 20 weeks ]
Not Provided
Not Provided
 
Behavioral Self-Regulation
Behavioral Self-Regulation for Weight Loss in Young Adults

The purpose of this pilot study is to determine whether incorporating self-regulation training using daily weighing is efficacious within a behavioral weight loss program specifically targeting young adults.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Obesity
Behavioral: self-regulation
The current study involves a behavioral weight loss intervention tailored specifically to young adults. All participants receive calorie and activity prescriptions as well as training in behavior modification. In addition, one group receives training in self-regulation techniques using daily weighing.
  • Experimental: 1
    Participants in the behavioral self-regulation intervention will receive a modified standard treatment that incorporates daily weighing and training in self-regulation methods for weight loss. All treatment modules are adapted for a young adult age group.
    Intervention: Behavioral: self-regulation
  • Experimental: 2
    Participants in the Standard group will receive a brief version of standard behavioral weight loss treatment with treatment modules tailored to better meet the needs of young adults.
    Intervention: Behavioral: self-regulation
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
41
November 2007
November 2007   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • body mass index between 27 and 40
  • age between 21 and 35

Exclusion Criteria:

  • report a history of eating disorder or a current eating disorder
  • report a heart condition or other medical condition that would limit ability to participate in an exercise program without direct supervision from physician
  • report major psychiatric diseases or organic brain syndromes
  • currently participating in another weight loss program, are taking a weight loss medication, or have lost more than 5% of body weight curing last 6 months
  • pregnant, lactating, or less than 6 months post-partum
  • intend to move out of city within the time frame of the investigation or will miss multiple meetings during the study time frame
Both
18 Years to 35 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00488228
CMTT# 2096-07
Not Provided
The Miriam Hospital
The Miriam Hospital
Not Provided
Study Director: Jessica G LaRose, Ph.D. The Miriam Hospital
Principal Investigator: Rena R Wing, PhD The Miriam Hospital
The Miriam Hospital
January 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP