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Effectiveness of Cognitive-Affective Behavior Therapy for the Treatment of Somatization Disorder

Primary Purpose

Somatization Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Augmented Standard Medical Care
Cognitive-Affective Behavior Therapy
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Somatization Disorder focused on measuring Cognitive Behavior Therapy, Treatment Outcome, Health Care Utilization, Somatization Disorder, Somatoform Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meets DSM-IV criteria for somatization disorder Available for follow-up over the ensuing 18 months English-speaking Exclusion Criteria: Meets DSM-IV criteria for a psychotic disorder, organic brain syndrome, or psychoactive substance dependence (Other psychiatric comorbidity is not exclusionary) Active suicidal ideation Unstable major medical condition Plans to engage in additional psychotherapy during the first 6 months after enrollment Current use of any medication that has not been stabilized for the previous 2 months

Sites / Locations

  • Department of Psychiatry, Robert Wood Johnson Medical School

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Augmented Standard Medical Care

Cognitive-Affective Behavior Therapy

Arm Description

Participants will receive standard medical care augmented by a psychiatric consultation letter sent to the participants' primary care physician.

Participants will receive individually administered cognitive-affective behavior therapy as well as augmented standard medical care.

Outcomes

Primary Outcome Measures

Clinical Global Impression Scale for Somatization Disorder

Secondary Outcome Measures

Physical functioning
Health care utilization

Full Information

First Posted
September 6, 2005
Last Updated
February 19, 2014
Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00149760
Brief Title
Effectiveness of Cognitive-Affective Behavior Therapy for the Treatment of Somatization Disorder
Official Title
Cognitive Affective Behavior Therapy for Somatization
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
August 2003 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
February 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the long-term effect of cognitive-affective behavior therapy on the physical symptoms, functioning, and health care utilization of people with somatization disorder.
Detailed Description
Somatization disorder is a syndrome characterized by the presence of multiple medically unexplained physical symptoms. It often results in substantial functional impairment and the need for extensive medical treatment. Neither pharmacological nor psychosocial treatments for the disease have demonstrated clinical success. People with somatization disorder may benefit from a treatment that integrates emotion-centered strategies into cognitive behavioral therapy. The long-term effectiveness of this treatment has not been established, however. This study will examine the long-term effect of cognitive-affective behavior therapy on the physical symptoms, functioning, and health care utilization of people with somatization disorder. Participants in this open-label study will be randomly assigned to receive either cognitive-affective behavior therapy (CABT) or standard medical care that is augmented by a psychiatric consultation. Treatment will last 4 months. Assessments of somatic symptomatology, functional impairment, and health care costs will occur at screening, baseline (1 to 2 weeks after screening), and 4, 10, and 16 months after baseline. The visits at 10 and 16 months post-baseline will assess specifically the long-term efficacy of the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Somatization Disorder
Keywords
Cognitive Behavior Therapy, Treatment Outcome, Health Care Utilization, Somatization Disorder, Somatoform Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
88 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Augmented Standard Medical Care
Arm Type
Active Comparator
Arm Description
Participants will receive standard medical care augmented by a psychiatric consultation letter sent to the participants' primary care physician.
Arm Title
Cognitive-Affective Behavior Therapy
Arm Type
Experimental
Arm Description
Participants will receive individually administered cognitive-affective behavior therapy as well as augmented standard medical care.
Intervention Type
Behavioral
Intervention Name(s)
Augmented Standard Medical Care
Other Intervention Name(s)
Psychiatric consultation letter sent to primary physician
Intervention Description
Participants' physicians will receive a letter making specific treatment recommendations for primary care treatment.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Affective Behavior Therapy
Other Intervention Name(s)
Emotionally-Focused Cognitive-Behavioral Therapy
Intervention Description
Individually-administered cognitive-behavioral therapy with an emotional focus in addition to augmented standard medical care
Primary Outcome Measure Information:
Title
Clinical Global Impression Scale for Somatization Disorder
Time Frame
Measured at baseline and Months 4, 10, and 16
Secondary Outcome Measure Information:
Title
Physical functioning
Time Frame
Measured at baseline and Months 4, 10, and 16
Title
Health care utilization
Time Frame
Measured between Months 4 and 16

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV criteria for somatization disorder Available for follow-up over the ensuing 18 months English-speaking Exclusion Criteria: Meets DSM-IV criteria for a psychotic disorder, organic brain syndrome, or psychoactive substance dependence (Other psychiatric comorbidity is not exclusionary) Active suicidal ideation Unstable major medical condition Plans to engage in additional psychotherapy during the first 6 months after enrollment Current use of any medication that has not been stabilized for the previous 2 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lesley A. Allen, PhD
Organizational Affiliation
Department of Psychiatry, Robert Wood Johnson Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychiatry, Robert Wood Johnson Medical School
City
Piscataway
State/Province
New Jersey
ZIP/Postal Code
08854
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11764061
Citation
Allen LA, Woolfolk RL, Lehrer PM, Gara MA, Escobar JI. Cognitive behavior therapy for somatization disorder: a preliminary investigation. J Behav Ther Exp Psychiatry. 2001 Jun;32(2):53-62. doi: 10.1016/s0005-7916(01)00020-9.
Results Reference
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PubMed Identifier
12461199
Citation
Allen LA, Escobar JI, Lehrer PM, Gara MA, Woolfolk RL. Psychosocial treatments for multiple unexplained physical symptoms: a review of the literature. Psychosom Med. 2002 Nov-Dec;64(6):939-50. doi: 10.1097/01.psy.0000024231.11538.8f.
Results Reference
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Citation
Allen, Lesley A. Short-term therapy for somatization disorder: A cognitive behavioral approach. Journal of Cognitive Psychotherapy. Vol 14(4) Win 2000, 373-380.
Results Reference
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PubMed Identifier
16864762
Citation
Allen LA, Woolfolk RL, Escobar JI, Gara MA, Hamer RM. Cognitive-behavioral therapy for somatization disorder: a randomized controlled trial. Arch Intern Med. 2006 Jul 24;166(14):1512-8. doi: 10.1001/archinte.166.14.1512.
Results Reference
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Effectiveness of Cognitive-Affective Behavior Therapy for the Treatment of Somatization Disorder

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