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Published Online: 29 June 2017

A Randomized Controlled Trial of Medication and Cognitive-Behavioral Therapy for Hypochondriasis

Abstract

Objective:

Prior studies of hypochondriasis demonstrated benefits for pharmacotherapy and for cognitive-behavioral therapy (CBT). This study examined whether joint treatment offers additional benefit.

Method:

Patients with DSM-IV hypochondriasis (N=195) were randomly assigned to one of four treatments—placebo, CBT, fluoxetine, or joint treatment with both fluoxetine and CBT. Evaluations assessed hypochondriasis, other psychopathology, adverse events, functional status, and quality of life. The primary analysis assessed outcome at week 24 among the intent-to-treat sample, with responders defined as having a 25% or greater improvement over baseline on both the Whiteley Index and a modified version of the Yale-Brown Obsessive Compulsive Scale for hypochondriasis (H-YBOCS-M). The Cochran-Armitage trend test assessed the hypothesized pattern of response: joint treatment > CBT or fluoxetine treatment > placebo treatment.

Results:

The predicted pattern of response was statistically significant, as shown by the following responder rates: joint treatment group, 47.2%; single active treatment group, 41.8%; and placebo group, 29.6%. Responder rates for each active treatment were not significantly different from the rate for placebo. Secondary analyses of the Whiteley Index as a continuous measure revealed that, compared with placebo, fluoxetine (but not CBT) was significantly more effective at week 24 in reducing hypochondriasis and had a significantly faster rate of improvement over 24 weeks. Fluoxetine also resulted in significantly less anxiety and better quality of life than placebo. Dropout rates did not differ between groups, and treatment-emergent adverse events were evenly distributed.

Conclusions:

This study supports the safety, tolerance, and efficacy of fluoxetine for hypochondriasis. Joint treatment provided a small incremental benefit. Because approximately 50% of patients did not respond to the study treatments, new or more intensive approaches are needed.

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Supplementary Material

File (appi.ajp.2017.16020189.ds001.pdf)

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 756 - 764
PubMed: 28659038

History

Received: 13 February 2016
Revision received: 6 September 2016
Revision received: 4 February 2017
Revision received: 20 March 2017
Accepted: 10 April 2017
Published online: 29 June 2017
Published in print: August 01, 2017

Keywords

  1. Somatoform Disorders
  2. Clinical Drug Studies
  3. Drug-Psychotherapy Combination

Authors

Affiliations

Brian A. Fallon, M.D. [email protected]
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.
David K. Ahern, Ph.D.
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.
Martina Pavlicova, Ph.D.
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.
Iordan Slavov, Ph.D.
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.
Natalia Skritskya, Ph.D.
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.
Arthur J. Barsky, M.D.
From the New York State Psychiatric Institute, New York; and Brigham and Women’s Hospital, Boston.

Notes

Address correspondence to Dr. Fallon ([email protected]).
Presented at the 60th Annual Meeting of the Academy of Psychosomatic Medicine, Tucson, Nov. 13–16, 2013.

Competing Interests

The authors report no financial relationships with commercial interests.

Funding Information

National Institute of Mental Health10.13039/100000025: RO1 MH071456, RO1 MH071688
Supported by NIMH grants to Dr. Fallon (RO1 MH071456) and Dr. Barsky (RO1 MH071688).

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