Effectiveness of Behavioral Treatments for Obesity and Major Depression in Women
Primary Purpose
Depression, Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Weight loss treatment
Behavior therapy for depression
Health education counseling
Sponsored by

About this trial
This is an interventional treatment trial for Depression focused on measuring Depressive Disorder, Weight Loss, Behavioral Treatment, Behavior Therapy, Randomized Clinical Trial
Eligibility Criteria
Inclusion Criteria:
- Meets DSM-IV criteria for major depressive disorder
- Score of 12 to 24 on Hamilton Depression Rating Scale (HDRS)
- Body mass index (BMI) of 30 to 40 kg
Exclusion Criteria:
- Plans to move out of the area during the study
- Current smoker
- Diagnosis of bipolar disorder, a psychotic disorder, bulimia, or post-traumatic stress disorder
- Meets criteria for severe depression (HDRS score greater than 24)
- Diagnosis of type 1 or 2 diabetes
- Plans to have bariatric surgery during the study
- No access to a telephone
- Unable to walk unaided or unable to walk 1/4 mile without stopping
- Does not have written clearance from primary care physician for physical activity
- Presence of a condition that precludes dietary changes (e.g., ulcerative colitis, Crohn's disease, active diverticulitis, renal disease)
- Presence of medical conditions likely to limit lifespan
- Taking prescription weight loss medications
- Initiation of anti-depressant medication within the 3 months prior to study entry
- Taking mood stabilizers, antipsychotic medication, or medications known to affect appetite and/or weight (e.g., corticosteroids)
- Reports active suicidal ideation via SCID interview, a score of 3 on item 24 of the HDRS (active suicidal ideation), or determined to have suicidal potential by clinical staff
- Psychiatric hospitalization in the 12 months prior to study entry
- Currently receiving psychotherapy
Sites / Locations
- University of Massachusetts Medical School
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
1
2
Arm Description
Evidence-based behavioral weight loss treatment with health education counseling
Evidence-based behavioral weight loss treatment with brief behavior therapy for depression
Outcomes
Primary Outcome Measures
Change in body weight and the trend in body weight over time
Secondary Outcome Measures
Change in depression, physical activity, diet (daily caloric intake), psychosocial variables (anhedonia, exercise self-efficacy, disinhibited eating, quality of life), and cardiovascular risk factors (blood pressure, serum lipids, C-reactive protein)
Effect of potential mediators (adherence, depression, general and physical activity, caloric intake) on weight change
Full Information
NCT ID
NCT00572520
First Posted
December 11, 2007
Last Updated
July 2, 2018
Sponsor
University of Massachusetts, Worcester
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT00572520
Brief Title
Effectiveness of Behavioral Treatments for Obesity and Major Depression in Women
Official Title
Treating Co-morbid Obesity and Major Depressive Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
July 2007 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Massachusetts, Worcester
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will compare the effectiveness of two weight loss programs, one supplemented with health education and the other supplemented with behavioral counseling, in treating women who are depressed and overweight.
Detailed Description
Obesity is one of the most alarming current health problems in the United States, with 31% percent of the population considered obese. Previous studies have shown that there is a higher incidence of depression in people who are overweight. It is not known whether depression causes obesity or vice versa, but the association may stem from the stigma of obesity or from the appetite and weight gain caused by depressive symptoms. With the increased risk of cardiovascular and other life-threatening diseases from obesity, promotion of healthful habits is important. Providing the motivational skills to adhere to these habits is also crucial, especially in people who are both overweight and depressed. This study will compare the effectiveness of two weight loss programs, one supplemented with health education and the other supplemented with behavioral counseling, in treating women who are depressed and overweight.
Participants in this 2-year study will be divided into one of two treatment groups: one group will address weight loss and depression via nutrition, exercise, and health education and the other group will address weight loss and depression via nutrition, exercise, and behavioral counseling. Participants receiving health education will learn about women's health topics and receive tips on staying healthy and preventing disease. Participants receiving behavioral counseling will learn about depression and links between activity and mood. They will also be asked to keep a diary of moods and activities. Participants in both treatment groups will undergo the same schedule of study visits and assessments. A baseline visit will include blood tests; measurements of height, weight, waist size, and blood pressure; and completion of questionnaires about depression, eating habits, and physical activity. Next, over a 3-week period, participants will receive three phone calls asking about food intake from the previous day. In the first 6 months of the study, there will be a total of 26 weekly treatment visits. These visits will consist of ten 1-hour sessions with a counselor and sixteen 90-minute sessions with a dietician. During the next 6 months, participants will continue to meet with their dieticians monthly for a total of 6 visits and will receive monthly phone calls from their counselor. Quaterly phone calls with their counselor will continue in the second year of the study. There will be three check-in appointments similar to the baseline assessment, occurring at Month 6 and Years 1 and 2.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Obesity
Keywords
Depressive Disorder, Weight Loss, Behavioral Treatment, Behavior Therapy, Randomized Clinical Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
161 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Evidence-based behavioral weight loss treatment with health education counseling
Arm Title
2
Arm Type
Experimental
Arm Description
Evidence-based behavioral weight loss treatment with brief behavior therapy for depression
Intervention Type
Behavioral
Intervention Name(s)
Weight loss treatment
Intervention Description
Over 2 years, this treatment involves a total of 26 group visits and 10 individual visits with a health education counselor. Group visits, led by a registered dietitian and a licensed exercise physiologist, will target diet and physical activity.
Intervention Type
Behavioral
Intervention Name(s)
Behavior therapy for depression
Intervention Description
Behavior therapy for depression will be delivered by a trained behavior therapist. Participants receiving behavioral counseling will learn about depression, links between activity and mood, and will be asked to keep a diary of moods and activities.
Intervention Type
Behavioral
Intervention Name(s)
Health education counseling
Intervention Description
Health education counseling will be delivered by a trained health education counselor. Participants receiving health education will learn about women's health topics and receive tips on staying healthy and preventing disease.
Primary Outcome Measure Information:
Title
Change in body weight and the trend in body weight over time
Time Frame
Measured at Month 6 and Years 1 and 2
Secondary Outcome Measure Information:
Title
Change in depression, physical activity, diet (daily caloric intake), psychosocial variables (anhedonia, exercise self-efficacy, disinhibited eating, quality of life), and cardiovascular risk factors (blood pressure, serum lipids, C-reactive protein)
Time Frame
Measured at Year 2
Title
Effect of potential mediators (adherence, depression, general and physical activity, caloric intake) on weight change
Time Frame
Measured at Year 2
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Meets DSM-IV criteria for major depressive disorder
Score of 12 to 24 on Hamilton Depression Rating Scale (HDRS)
Body mass index (BMI) of 30 to 40 kg
Exclusion Criteria:
Plans to move out of the area during the study
Current smoker
Diagnosis of bipolar disorder, a psychotic disorder, bulimia, or post-traumatic stress disorder
Meets criteria for severe depression (HDRS score greater than 24)
Diagnosis of type 1 or 2 diabetes
Plans to have bariatric surgery during the study
No access to a telephone
Unable to walk unaided or unable to walk 1/4 mile without stopping
Does not have written clearance from primary care physician for physical activity
Presence of a condition that precludes dietary changes (e.g., ulcerative colitis, Crohn's disease, active diverticulitis, renal disease)
Presence of medical conditions likely to limit lifespan
Taking prescription weight loss medications
Initiation of anti-depressant medication within the 3 months prior to study entry
Taking mood stabilizers, antipsychotic medication, or medications known to affect appetite and/or weight (e.g., corticosteroids)
Reports active suicidal ideation via SCID interview, a score of 3 on item 24 of the HDRS (active suicidal ideation), or determined to have suicidal potential by clinical staff
Psychiatric hospitalization in the 12 months prior to study entry
Currently receiving psychotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sherry L. Pagoto, PhD
Organizational Affiliation
University of Massachusetts, Worcester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Medical School
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
18793398
Citation
Schneider KL, Bodenlos JS, Ma Y, Olendzki B, Oleski J, Merriam P, Crawford S, Ockene IS, Pagoto SL. Design and methods for a randomized clinical trial treating comorbid obesity and major depressive disorder. BMC Psychiatry. 2008 Sep 15;8:77. doi: 10.1186/1471-244X-8-77.
Results Reference
derived
Learn more about this trial
Effectiveness of Behavioral Treatments for Obesity and Major Depression in Women
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