The cognitive behavioural group training: 1. increases quality of life; 2. decreases direct costs due to health care utilization; 3. decreases indirect costs due to productivity loss; 4. decreases overall psychological distress.
ID
Bron
Verkorte titel
Aandoening
1. Unexplained Physical Symptoms
2. Undifferentiatied Somatoform Disorder
3. Chronic Pain Disorder
4. Somatoform Disorders
Onverklaarde Lichamelijke Klachten
Ongedifferentieerde Somatoforme Stoornis
Pijnstoornis
Somatoforme Stoornissen
Ondersteuning
Riagg Rijnmond
Westhavenkade 85
3133 AV Vlaardingen
The Netherlands
Prof. dr. J. Passchier, supervisor of the Ph.D.student
Erasmus MC
Department of Medical Psychology and Psychotherapy
PO Box 2040
3000 CA Rotterdam
The Netherlands
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary outcome is effectiveness of the group training. This effectiveness is operationalised with quality of life. Quality of life is measured with the 36-item Short Form Health Survey (SF-36), which is administered at baseline, after the group therapy/waiting list, 3 months after the group training and one year after the group training.
Achtergrond van het onderzoek
After medical examination, physicians classify 20 to 74% of patients’ symptoms as Unexplained Physical Symptoms (UPS). When UPS persists, cognitive-behavioural therapy may be considered. The cognitive-behavioural therapy based on the consequences model, in which various forms of psychosocial stress are labelled as consequences rather than causes of UPS, has shown to be more acceptable for patients than a therapy based on a causal model. Eighty percent of the patients with UPS accepted an individual therapy based on this model and effectiveness has been shown when applied in secondary medical care, while only 10% of the mental health referrals leads to treatment. However, when the applicability of this model is examined in primary medical care, the high acceptance showed a drastic drop. We modified the implementation of the consequences model into a standardized training program conducted by Riagg Rijnmond, a mental health institution. In this modified program, we standardised the protocol for the individual therapy suitable for patients’ personal needs into a group training, in which the consequences model is used bottom-up instead of top-down. We assume that this innovative implementation is acceptable to patients, as it legitimates the existence of consequences, in other words, the patients are exonerated. The objective of this randomised controlled study is to assess applicability and (cost-)effectiveness of this particular cognitive behavioural group training. If we show that this group training is applicable and (cost-)effective, more patients with UPS could be served on a (cost-)effective basis.
Doel van het onderzoek
The cognitive behavioural group training:
1. increases quality of life;
2. decreases direct costs due to health care utilization;
3. decreases indirect costs due to productivity loss;
4. decreases overall psychological distress.
Onderzoeksopzet
T1: baseline assessment;
(inclusion: up to September 2008);
T2: assessment after training/waiting list;
T3: assessment three month after training;
T4: assessement one year after training.
Onderzoeksproduct en/of interventie
The experimental condition is a cognitive behavioural group training consisting of thirteen ad verbatim protocollised weekly sessions of two hours each.
The control condition is a waiting list.
Algemeen / deelnemers
Westhavenkade 85
3133 AV Vlaardingen
The Netherlands)
Erasmus MC
Department of Medical Psychology and Psychotherapy
PO Box 2040
Lyonne Zonneveld
Rotterdam 3000 CA
The Netherlands
(+31) 10 4453426
LZonneveld@riaggrijnmond.nl
Wetenschappers
Westhavenkade 85
3133 AV Vlaardingen
The Netherlands)
Erasmus MC
Department of Medical Psychology and Psychotherapy
PO Box 2040
Lyonne Zonneveld
Rotterdam 3000 CA
The Netherlands
(+31) 10 4453426
LZonneveld@riaggrijnmond.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age between 18 and 65 years;
2. being able to speak, read and write Dutch;
3. at least 6 months duration of the Unexplained Physical Symptoms (UPS);
4. UPS can be classified as DSM-IV-TR Undifferentiated Somatoform Disorder or Pain Disorder;
5. written informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Undifferentiated Somatoform Disorder or Chronic Pain Disorder is not the principal DSM-IV-TR classification;
2. UPS is not the principal somatic disease;
3. handicaps like cognitive mental impairment and blindness hinder the patient to participate in the training.
Opzet
Deelname
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In overige registers
Register | ID |
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NTR-new | NL1538 |
NTR-old | NTR1609 |
Ander register | METC Erasmus MC : MEC-2004-191 |
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