Evidence map›Paper›PMID 28659038›Full record

Trial reportThe American journal of psychiatry2017

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

Brian A Fallon, David K Ahern, Martina Pavlicova, Iordan Slavov, Natalia Skritskya, Arthur J Barsky

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in The American journal of psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 65 citations in OpenAlex.

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  15. Why health anxiety needs to be recognised in hospital practice.Clinical medicine (London, England) · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Brian A FallonFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
David K AhernFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
Martina PavlicovaFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
Iordan SlavovFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
Natalia SkritskyaFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
Arthur J BarskyFrom the New York State Psychiatric Institute, New York; and Brigham and Women's Hospital, Boston.
Brigham and Women's Hospital · US

Funding

Treatment of Hypochondriasis with CBT &/or SSRIR01MH071456 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI FALLON, BRIAN A. · 2006 to 2010
$2.4M
Treatment of Hypochondriasis with CBT and/or SSRIR01MH071688 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI BARSKY, ARTHUR JOSEPH · 2006 to 2010
$2.3M
NIMH NIH HHS R01 MH071456NIMH NIH HHS R01 MH071688
6 · The paper itself

Abstract

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

methodPatients 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.

resultsThe 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.

conclusionsThis 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.

Indexed as

AdultAgedCognitive Behavioral TherapyCombined Modality TherapyFemaleFluoxetineHumansHypochondriasisMaleMiddle AgedQuality of LifeYoung AdultFluoxetineClinical Drug StudiesDrug-Psychotherapy CombinationSomatoform Disorders

Identifiers

PMID28659038
PMCPMC5957509
OpenAlexW2731875168

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.