search
Back to results

Addressing Emotional and Cognitive Factors in Behavioral Weight Loss Treatment (Part 2)

Primary Purpose

Overweight, Obesity

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standard Behavioral Weight Loss Treatment with Affective and Cognitive Skills Training
Standard Behavioral Weight Loss Treatment
Sponsored by
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight focused on measuring Weight loss

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 21 and 70 years
  • Body mass index between 27 and 40
  • Score 5 or above on the internal disinhibition scale of the Eating Inventory

Exclusion Criteria:

  • Are currently participating in a weight loss program and/or are taking a weight loss medication or lost greater than or equal to 5% of body weight during the past six months
  • Are pregnant, lactating, less than 6 months postpartum or plan to become pregnant during the time frame of the investigation
  • Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals endorsing joint problems, prescription medication usage, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.

Sites / Locations

  • The Weight Control and Diabetes Research Center, The Miriam Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Standard behavioral weight loss treatment with cognitive and affective skills training

Standard behavioral weight loss treatment

Outcomes

Primary Outcome Measures

Weight Loss

Secondary Outcome Measures

Internal disinhibition as measured by the Eating Inventory
Physical activity as measured by the Paffenbarger
Dietary intake as measured by the Block Food Frequency Questionnaire

Full Information

First Posted
November 13, 2007
Last Updated
March 12, 2018
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
search

1. Study Identification

Unique Protocol Identification Number
NCT00558194
Brief Title
Addressing Emotional and Cognitive Factors in Behavioral Weight Loss Treatment (Part 2)
Official Title
Addressing Emotional and Cognitive Factors in Behavioral Weight Loss Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of funds
Study Start Date
August 2009 (undefined)
Primary Completion Date
January 2011 (Anticipated)
Study Completion Date
January 2011 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Behavioral weight loss, the current treatment of choice for moderate obesity, achieves impressive short term results, however, weight regain following treatment is a major problem. Over 50% of participants in behavioral weight loss programs report difficulty with internal antecedents to unhealthy weight control behaviors and this difficulty is associated with weight regain following treatment. Current treatment approaches do not adequately address these antecedents. The aim of this series of studies is to develop, implement, and evaluate a behavioral weight loss program modified to provide participants with skills to deal effectively with affective and cognitive difficulties. The study targets men and women with BMI of 27-40 who self-report difficulty with emotional and/or cognitive antecedents to unhealthy weight control behaviors. The study will randomize 120 participants to receive 12 months of standard behavioral therapy for weight loss or standard behavioral treatment plus affective and cognitive skills training. The long-term goal of this research is to improve the weight loss maintenance outcomes of behavioral weight loss programs by addressing affective and cognitive antecedents to unhealthy weight control behaviors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight, Obesity
Keywords
Weight loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Standard behavioral weight loss treatment with cognitive and affective skills training
Arm Title
2
Arm Type
Active Comparator
Arm Description
Standard behavioral weight loss treatment
Intervention Type
Behavioral
Intervention Name(s)
Standard Behavioral Weight Loss Treatment with Affective and Cognitive Skills Training
Intervention Description
12-month (6-month weekly, 3-month biweekly, 3-month monthly) group treatment
Intervention Type
Behavioral
Intervention Name(s)
Standard Behavioral Weight Loss Treatment
Intervention Description
12-month (6-month weekly, 3-month biweekly, 3-month monthly) group treatment
Primary Outcome Measure Information:
Title
Weight Loss
Time Frame
12 Months
Secondary Outcome Measure Information:
Title
Internal disinhibition as measured by the Eating Inventory
Time Frame
12 Months
Title
Physical activity as measured by the Paffenbarger
Time Frame
12 months
Title
Dietary intake as measured by the Block Food Frequency Questionnaire
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 21 and 70 years Body mass index between 27 and 40 Score 5 or above on the internal disinhibition scale of the Eating Inventory Exclusion Criteria: Are currently participating in a weight loss program and/or are taking a weight loss medication or lost greater than or equal to 5% of body weight during the past six months Are pregnant, lactating, less than 6 months postpartum or plan to become pregnant during the time frame of the investigation Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals endorsing joint problems, prescription medication usage, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heather M. Niemeier, Ph.D.
Organizational Affiliation
The Miriam Hospital/The Warren Alpert Medical School of Brown U niversity
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Weight Control and Diabetes Research Center, The Miriam Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Addressing Emotional and Cognitive Factors in Behavioral Weight Loss Treatment (Part 2)

We'll reach out to this number within 24 hrs