Acceptance and Commitment Group Therapy (ACT) for Patients With Health Anxiety (ACT)

April 12, 2013 updated by: University of Aarhus

Treatment of Patients With Health Anxiety. A Randomized Controlled Trial of Acceptance and Commitment Therapy (ACT) Group Treatment Compared to a Waiting List

The purpose of this study is to determine the effect of Acceptance and Commitment Therapy (ACT) in groups on functional level, emotional problems, and use of health care in patients with severe health anxiety in a randomized, controlled design.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Health anxiety disorder or Hypochondriasis is a prevalent somatoform disorder, but a rarely used diagnosis in clinical practice despite studies having reported prevalence between 0.8-9.5% in primary care (Fink et al, 2004). As a consequence, the disorder is rarely treated.

The lack of valid, reliable, and generally accepted diagnostic criteria has been a major obstacle in clinical practice and Hypochondriasis studies, which causes problems particularly in distinguishing Hypochondriasis patients from other patients presenting with medically unexplained symptoms or functional symptoms.

In 2004, the investigators introduced a radically revised definition of Hypochondriasis. Hypochondriasis is viewed as a stigmatizing label, and the designation health anxiety has been suggested as replacement. This new diagnosis is empirically established. The essential feature of health anxiety is that the patients present with cognitive symptoms such as unfounded worrying about their health. In contrast to other somatoform disorders, the patients are not necessarily plagued by physical symptoms.

The new diagnostic criteria include the symptom 'obsessive rumination about illness' plus at least one of the symptoms 'worry or preoccupation with fears of harboring an illness or with bodily functions', 'suggestibility or autosuggestibility', 'an unrealistic fear of being infected or contaminated', 'an excessive fascination with medical information', or 'fear of taking prescribed medication'.

In the current study, health anxiety is diagnosed by use of newly introduced empirically established positive criteria for Health anxiety (Fink et al, 2004).

Most patients with health anxiety disorder receive the majority of their care in primary care settings. They are often unhappy with the services they receive, and primary care providers often feel unprepared to address symptoms that primarily appear functional.

During the past 5 years, the investigators have treated patients suffering from severe functional disorder (i.e. Bodily distress syndrome or Somatization disorder) in randomized controlled trials (RCTs) - at the Research Clinic. The investigators reject many patients suffering from health anxiety, who have no other treatment opportunities, and there is an impending need for treatment opportunities. The investigators research group has done research in epidemiology, psychopathology and diagnostics of Health anxiety, and the investigators are part of international networks regarding the revision of the diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorders V (DSM-V) and the International Classification of Diseases 11 (ICD-11).

RCTs have shown that Cognitive Behavioral Therapy (CBT) has effect on health anxiety (Barsky & Ahern, 2004; Greeven et al., 2007), and one of the trials also showed effect of anti-depressant medication (Greeven et al., 2007).

In general, the treatment of health anxiety is sparsely investigated both as to psychotherapy and medical treatment.

The investigators wish to examine the effect of Acceptance and Commitment Therapy (ACT) in groups on functional level, emotional problems, and use of health care in patients with severe health anxiety in a randomized, controlled design.

Health anxiety disorder is a burden for the sufferers and costly for society due to lost working years because of early onset of the disorder and high health care costs. The development of evidence-based treatment offering these patients the same professional treatment as patients with other disorders may lead to better quality of life for the patients and reduction in health care costs.

Study Type

Interventional

Enrollment (Actual)

126

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Aarhus C, Denmark, 8000
        • The Research Clinic for Functional Disorders, Aarhus University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 58 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Whiteley-7 score on 21,4 or more (scale 0-100 score points).
  2. Severe health anxiety (diagnosed by SCAN interview).
  3. Age 20-60 years
  4. Patients of Scandinavian origin who understand, read, write and speak Danish.
  5. No lifetime-diagnosis of psychoses, bipolar affective disorder or depression with psychotic symptoms (ICD-10: F20-29, F30-31, F32.3, F33.3)
  6. In case of a co morbid functional or other psychiatric disorder health anxiety must be the dominating problem.

Exclusion criteria:

  1. Another severe psychiatric disorder or if the patient is suicidal.
  2. Abuse of narcotics or alcohol and (non-prescribed) medicine.
  3. Pregnancy.
  4. No informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: ACT group therapy

Third generation cognitive behavioral therapy

Group therapy (ACT) in groups of 9 patients in 9 weekly 3.5-hours sessions & 1 booster session 1 month after 9th session, a total of 35.5 hours

Group therapy (ACT) in groups of 9 patients in 9 weekly 3.5-hours sessions & 1 booster session 1 month after 9th session, a total of 35.5 hours
Other Names:
  • Third generation cognitive behavioral therapy
No Intervention: Control
Control group assigned to wait list (treatment as usual). After 9 months they are offered ACT group therapy, but not as part of the research project.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Health anxiety measured by the Whiteley-7 index
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)

Secondary Outcome Measures

Outcome Measure
Time Frame
Social level of functioning measured with Short Form health status questionnaire from the medical outcome status (SF-36)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Social level of functioning, emotional disorders measured with relevant sub-scales from Symptom Check List, 90 items (SCL 90)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Social level of functioning measured with an alcohol dependency questionnaire (CAGE)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Illness perception measured with Illness Perception Questionnaire (IPQ)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Physical symptoms measured with somatisation subscales from Symptom Check List, 90 items (SCL 90)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Health care use (National Patient Register & National Health Service Register (general practitioner (GP) contacts/consultations, specialists, physiotherapists, dentists, GPs' emergency service), The Danish Medicine Agency (medicine consumption)).
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
Sick days (the DREAM database - the register-based evaluation of the extent of marginalization)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
ACT process measures measured with Five Facet Mindfulness Questionnaire (FFMQ)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)
ACT process measures measured with Acceptance and Action Questionnaire - II (AAQ II)
Time Frame: 9 months (2nd follow-up)
9 months (2nd follow-up)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Per Fink, DMSc, The Research Clinic for Functional Disorders and Psychosomatics, Aarhus University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2010

Primary Completion (Actual)

April 1, 2013

Study Completion (Actual)

April 1, 2013

Study Registration Dates

First Submitted

February 16, 2010

First Submitted That Met QC Criteria

July 7, 2010

First Posted (Estimate)

July 8, 2010

Study Record Updates

Last Update Posted (Estimate)

April 15, 2013

Last Update Submitted That Met QC Criteria

April 12, 2013

Last Verified

April 1, 2013

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2001001

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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