Cognitive Behavioral Treatments for Depression in Chronic Illness
Primary Purpose
Major Depression
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Conventional cognitive behavioral therapy
Religious cognitive behavioral therapy
Sponsored by
About this trial
This is an interventional treatment trial for Major Depression focused on measuring Depression
Eligibility Criteria
Inclusion Criteria:
- chronic disabling medical illness
- religion at least somewhat important to patient
- major depressive disorder by MINI neuropsychiatric interview
- Beck Depression Inventory scores of 16-28 (moderately severe depression)
- live near Durham, North Carolina, or near Glendale, in Southern California
Exclusion Criteria:
- significant cognitive impairment
- significant suicidal thoughts or risk
- no access to telephone
Sites / Locations
- Glendale Adventist Medical Center
- Duke University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Conventional cognitive behavioral therapy
Religious cognitive behavioral therapy
Arm Description
Subjects randomized to this arm will receive conventional cognitive behavioral therapy for the treatment of major depression
Subjects randomized to this arm will receive conventional cognitive behavioral therapy, but their religious beliefs will be utilized as a resource in the therapy
Outcomes
Primary Outcome Measures
Beck Depression Inventory
Quantitative assessment of depressive symptoms
Beck Depression Inventory
Quantitative assessment of depressive symptoms
Beck Depression Inventory
Quantitative assessment of depressive symptoms
Beck Depression Inventory
Quantitative assessment of depressive symptoms
Beck Depression Inventory
Quantitative assessment of depressive symptoms
Secondary Outcome Measures
Duke Social Support Index (abbreviated)
Measures amount of social support and satisfaction with it.
Duke Social Support Index (abbreviated)
Measures amount of social support and satisfaction with it
Duke Social Support Index
Measures amount of social support and satisfaction with it.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01208428
Brief Title
Cognitive Behavioral Treatments for Depression in Chronic Illness
Official Title
Cognitive Behavioral Treatments for Depression in Patients With Chronic Illness
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
August 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Duke University Medical Center in collaboration with Glendale Adventist Medical Center propose a randomized clinical trial of conventional cognitive behavior therapy (CCBT) vs. religious cognitive behavior therapy (RCBT) for major depression in medical patients with chronic disabling illness. Therapists will deliver the treatment in real time over the Internet and/or by telephone to increase treatment access. This planning grant seeks support for a two-site study (North Carolina and California) that consists of two phases. In Phase I (Rounsaville 1a) the investigators will conduct an open trial of 30 patients to assess subject recruitment, refine RCBT and CCBT manuals and protocol, assess compliance with treatment, acceptability of treatment and delivery system (online vs. telephone), and allow therapists gain experience with delivery system and RCBT.
In Phase II (Rounsaville 1b) the investigators will conduct a randomized proof of concept comparison of CCBT vs. RCBT that will demonstrate feasibility and confirm the expected clinically meaningful difference for a definitive R01 application. In Phase II, 70 religious patients ages 18-85 with a new episode of major depression (MINI), scores of 16-35 on the Beck Depression Inventory (BDI), and at least one chronic disabling medical illness will be randomized to either CCBT or RCBT. The trial will consist of ten 50 min sessions administered by master's level therapists and delivered over 12 weeks. The primary endpoint will be BDI score at baseline, 4, 8, 12, and 24-week follow-up. Christian, Jewish, Hindu, Buddhist, and Muslim versions of the RCBT manual will be developed, and CBT experts in each of these traditions will supervise therapists delivering the intervention to patients from these faith traditions.
The purpose of this study is to determine feasibility and effect sizes for a future, fully powered treatment study. The importance is that results will be relevant to therapists well beyond those who explicitly practice pastoral counseling, extending to many secular therapists as well. If 65% of Americans indicate that religion is an important part of daily life and the vast majority of chronically ill medical patients wish to include it in their therapy, then all therapists (whether they have explicit training in pastoral counseling or not) are likely to encounter patients in which this approach would be applicable.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression
Keywords
Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
132 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Conventional cognitive behavioral therapy
Arm Type
Active Comparator
Arm Description
Subjects randomized to this arm will receive conventional cognitive behavioral therapy for the treatment of major depression
Arm Title
Religious cognitive behavioral therapy
Arm Type
Experimental
Arm Description
Subjects randomized to this arm will receive conventional cognitive behavioral therapy, but their religious beliefs will be utilized as a resource in the therapy
Intervention Type
Behavioral
Intervention Name(s)
Conventional cognitive behavioral therapy
Intervention Description
Conventional cognitive behavioral therapy is a standard treatment for depression. There will be ten 50-minute sessions delivered.
Intervention Type
Behavioral
Intervention Name(s)
Religious cognitive behavioral therapy
Intervention Description
Religious cognitive behavioral therapy is conventional cognitive behavioral therapy that includes consideration of the patient's religious beliefs in therapy. Subjects will receive ten 50-min sessions of therapy
Primary Outcome Measure Information:
Title
Beck Depression Inventory
Description
Quantitative assessment of depressive symptoms
Time Frame
Baseline
Title
Beck Depression Inventory
Description
Quantitative assessment of depressive symptoms
Time Frame
4 weeks
Title
Beck Depression Inventory
Description
Quantitative assessment of depressive symptoms
Time Frame
8 weeks
Title
Beck Depression Inventory
Description
Quantitative assessment of depressive symptoms
Time Frame
12 weeks
Title
Beck Depression Inventory
Description
Quantitative assessment of depressive symptoms
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Duke Social Support Index (abbreviated)
Description
Measures amount of social support and satisfaction with it.
Time Frame
Baseline
Title
Duke Social Support Index (abbreviated)
Description
Measures amount of social support and satisfaction with it
Time Frame
12 weeks
Title
Duke Social Support Index
Description
Measures amount of social support and satisfaction with it.
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
chronic disabling medical illness
religion at least somewhat important to patient
major depressive disorder by MINI neuropsychiatric interview
Beck Depression Inventory scores of 16-28 (moderately severe depression)
live near Durham, North Carolina, or near Glendale, in Southern California
Exclusion Criteria:
significant cognitive impairment
significant suicidal thoughts or risk
no access to telephone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harold G Koenig, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Glendale Adventist Medical Center
City
Glendale
State/Province
California
ZIP/Postal Code
91201
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
1556292
Citation
Propst LR, Ostrom R, Watkins P, Dean T, Mashburn D. Comparative efficacy of religious and nonreligious cognitive-behavioral therapy for the treatment of clinical depression in religious individuals. J Consult Clin Psychol. 1992 Feb;60(1):94-103. doi: 10.1037//0022-006x.60.1.94.
Results Reference
background
PubMed Identifier
17502804
Citation
Koenig HG. Religion and remission of depression in medical inpatients with heart failure/pulmonary disease. J Nerv Ment Dis. 2007 May;195(5):389-95. doi: 10.1097/NMD.0b013e31802f58e3.
Results Reference
background
PubMed Identifier
9546001
Citation
Koenig HG, George LK, Peterson BL. Religiosity and remission of depression in medically ill older patients. Am J Psychiatry. 1998 Apr;155(4):536-42. doi: 10.1176/ajp.155.4.536.
Results Reference
background
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Cognitive Behavioral Treatments for Depression in Chronic Illness
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