Applying Social Comparison Theory to Behavioral Weight Loss: Does Modifying Group Membership Improve Outcome? - Full Text View

Sponsored by:	The Miriam Hospital
Information provided by:	The Miriam Hospital
ClinicalTrials.gov Identifier:	NCT00716027

Purpose

The purpose of this study is to determine whether a modified behavioral treatment for weight loss that includes one-on-one treatment for individuals struggling to lose weight is associated with more weight loss than a standard behavioral treatment.

Condition	Intervention
Obesity	Behavioral: Standard behavioral treatment for weight loss Behavioral: Modified behavioral treatment for weight loss

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:	Applying Social Comparison Theory to Behavioral Weight Loss: Does Modifying Group Membership Improve Outcome?

Resource links provided by NLM:

MedlinePlus related topics: Obesity Weight Control

U.S. FDA Resources

Further study details as provided by The Miriam Hospital:

Primary Outcome Measures:

weight [ Time Frame: weekly for 24-weeks ] [ Designated as safety issue: No ]

Estimated Enrollment:	80
Study Start Date:	July 2008
Estimated Primary Completion Date:	February 2009 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
1: Active Comparator A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.	Behavioral: Standard behavioral treatment for weight loss A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.
2: Experimental A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.	Behavioral: Modified behavioral treatment for weight loss A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.

Arms

Assigned Interventions

1: Active Comparator

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.

Behavioral: Standard behavioral treatment for weight loss

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.

2: Experimental

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.

Behavioral: Modified behavioral treatment for weight loss

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.

Eligibility

Ages Eligible for Study:	21 Years to 70 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

BMI between 27 and 45 kg/m2

Exclusion Criteria:

participating in a weight loss program or taking a weight loss medication
currently pregnant, lactating, or less than 6-months post-partum or plan to become pregnant during the time of the intervention.
report a heart condition, chest pain during periods of activity or rest, or loss of consciousness
report conditions that would render the participant unlikely to follow the study protocol (e.g., terminal illness, relocation, substance abuse, sever psychiatric condition, dementia).

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00716027

Contacts

Contact: Tricia M Leahey, PhD

4017938947

TLeahey@Lifespan.org

Locations

United States, Rhode Island
The Miriam Hospital
Providence, Rhode Island, United States, 02903

Sponsors and Collaborators

The Miriam Hospital

Investigators

Principal Investigator:

Rena R Wing, PhD

The Miriam Hospital

More Information

No publications provided

Responsible Party:	The Miriam Hospital ( Rena R. Wing, PhD )
Study ID Numbers:	2034-08
Study First Received:	July 15, 2008
Last Updated:	July 15, 2008
ClinicalTrials.gov Identifier:	NCT00716027 History of Changes
Health Authority:	United States: Institutional Review Board

Study placed in the following topic categories:

Body Weight
Signs and Symptoms
Obesity
Weight Loss

Body Weight Changes
Nutrition Disorders
Overweight
Overnutrition

Additional relevant MeSH terms:

Body Weight
Signs and Symptoms
Obesity
Weight Loss

Body Weight Changes
Nutrition Disorders
Overweight
Overnutrition

ClinicalTrials.gov processed this record on September 10, 2009