Effective group training for patients with unexplained physical symptoms: a randomized controlled trial with a non-randomized one-year follow-up
- PMID: 22880056
- PMCID: PMC3413637
- DOI: 10.1371/journal.pone.0042629
Effective group training for patients with unexplained physical symptoms: a randomized controlled trial with a non-randomized one-year follow-up
Erratum in
- PLoS One. 2013;8(5). doi:10.1371/annotation/9cefaaa9-c367-4f2d-a927-0a0b304ae21f
Abstract
Background: Although cognitive-behavioral therapy for Unexplained Physical Symptoms (UPS) is effective in secondary care, studies done in primary care produced implementation problems and conflicting results. We evaluated the effectiveness of a cognitive-behavioral group training tailored to primary care patients and provided by a secondary community mental-health service reaching out into primary care.
Methodology/principal findings: The effectiveness of this training was explored in a randomized controlled trial. In this trial, 162 patients with UPS classified as undifferentiated somatoform disorder or as chronic pain disorder were randomized either to the training or a waiting list. Both lasted 13 weeks. The preservation of the training's effect was analyzed in non-randomized follow-ups, for which the waiting group started the training after the waiting period. All patients attended the training were followed-up after three months and again after one year. The primary outcomes were the physical and the mental summary scales of the SF-36. Secondary outcomes were the other SF-36-scales and the SCL-90-R. The courses of the training's effects in the randomized controlled trial and the follow-ups were analyzed with linear mixed modeling. In the randomized controlled trial, the training had a significantly positive effect on the quality of life in the physical domain (Cohen's d = 0.38;p = .002), but this overall effect was not found in the mental domain. Regarding the secondary outcomes, the training resulted in reporting an improved physical (Cohen's d = 0.43;p = 0.01), emotional (Cohen's d = 0.44;p = 0.01), and social (Cohen's d = 0.36;p = 0.01) functioning, less pain and better functioning despite pain (Cohen's d = 0.51;p = <0.001), less physical symptoms (Cohen's d = -.23;p = 0.05) and less sleep difficulties (Cohen's d = -0.25;p = 0.04) than time in the waiting group. During the non-randomized follow-ups, there were no relapses.
Conclusions/significance: The cognitive-behavioral group training tailored for UPS in primary care and provided by an outreaching secondary mental-health service appears to be effective and to broaden the accessibility of treatment for UPS.
Trial registration: TrialRegister.nl NTR1609 <rctview.asp?TC = 1609>
Conflict of interest statement
Figures
References
-
- De Waal MWM, Arnold IA, Eekhof JAH, Van Hemert AM (2004) Somatoform disorders in general practice: prevalence, functional impairment and comorbidity with anxiety and depressive disorders. British Journal of Psychiatry 184: 470–476. - PubMed
-
- Escobar JI, Waitzkin H, Silver RC, Gara M, Holman A (1998) Abridged somatization: a study in primary care. Psychosomatic Medicine 60: 466–472. - PubMed
-
- Kooiman CG, Bolk JH, Brand R, Trijsburg RW, Rooijmans HG (2000) Is alexithymia a risk factor for unexplained physical symptoms in general medical outpatients? Psychosomatic Medicine 62: 768–778. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous
