Somatization Disorder Clinical Trial
Official title:
Treatment of Patients With Chronic Functional Disorders. A Randomized Controlled Trial of Specialized Treatment Compared to Usual Care.
The purpose of this study is to determine the effect of specialized treatment (including cognitive therapy, social counselling and a recommendation letter to the patients' primary care physician) on the functional level, emotional problems, and use of health care in patients with chronic medically unexplained symptoms.
Status | Completed |
Enrollment | 120 |
Est. completion date | September 2008 |
Est. primary completion date | September 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Multiple somatic symptoms from several organ systems, without adequate medical explanation. - Moderate to severe influence on daily life. - The disorder's functional component can easily be separated from a possible well-defined chronic somatic illness. - No lifetime-diagnosis of psychoses, bipolar affective disorder or depression with psychotic symptoms (International Classification of Diseases [ICD-10]: F20-29, F30-31, F32.3, F33.3) - The condition must have been present for at least 2 years. - Patients of Scandinavian origin who understand, read, write and speak Danish. Exclusion Criteria: - No informed consent. - An acute psychiatric disorder that demands other treatment, or if the patient is suicidal. - Abuse of narcotics or alcohol and (non-prescribed) medicine. - Pregnancy. - Current industrial injury case or other action for damages. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Denmark | Per Fink | Aarhus C |
Lead Sponsor | Collaborator |
---|---|
University of Aarhus | Aarhus County, Denmark, Aarhus University Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Physical health measured with The Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) (aggregate score of the scales physical functioning, bodily pain and vitality) | Measured at baseline and months 4 (end of treatment), 10 and 16 | No | |
Secondary | Psychosocial effect measures: Social level of functioning, emotional disorders, coping strategies measured with relevant sub-scales from the SF-36, WHO-DAS II, CSQ, Symptom Checklist SCL, Whiteley-7 | Measured at baseline and months 4 (end of treatment), 10 and 16 | No | |
Secondary | Use of health care measured by information from the National Patient Register, the Psychiatric Central Register, the National Health Service Register and The Danish Medicines Agency | Measured for a period of one year prior to referral (baseline) and a period of one year after treatment | No |
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