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Completed

NCT Number: NCT01208428

Cognitive Behavioral Treatments for Depression in Chronic Illness

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.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Glendale Adventist Medical Center, Glendale, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Conventional cognitive behavioral therapy

Behavioral

Conventional cognitive behavioral therapy is a standard treatment for depression. There will be ten 50-minute sessions delivered.

Religious cognitive behavioral therapy

Behavioral

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 outcomes

  1. Beck Depression Inventory

    Time frame: Baseline

    Quantitative assessment of depressive symptoms

  2. Beck Depression Inventory

    Time frame: 4 weeks

    Quantitative assessment of depressive symptoms

  3. Beck Depression Inventory

    Time frame: 8 weeks

    Quantitative assessment of depressive symptoms

  4. Beck Depression Inventory

    Time frame: 12 weeks

    Quantitative assessment of depressive symptoms

  5. Beck Depression Inventory

    Time frame: 24 weeks

    Quantitative assessment of depressive symptoms

Secondary outcomes

  1. Duke Social Support Index (abbreviated)

    Time frame: Baseline

    Measures amount of social support and satisfaction with it.

  2. Duke Social Support Index (abbreviated)

    Time frame: 12 weeks

    Measures amount of social support and satisfaction with it

  3. Duke Social Support Index

    Time frame: 24 weeks

    Measures amount of social support and satisfaction with it.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

Cognitive Behavioral Treatments for Depression in Patients With Chronic Illness

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Sep 24, 2010
Registry last updated
Mar 17, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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