Effective Group Training for Patients with Unexplained Physical Symptoms: A Randomized Controlled Trial with a Non-Randomized One-Year Follow-Up

被引:20
|
作者
Zonneveld, Lyonne N. L. [1 ,2 ,3 ]
van Rood, Yanda R. [4 ]
Timman, Reinier [3 ]
Kooiman, Cornelis G. [5 ]
van't Spijker, Adriaan [3 ]
Busschbach, Jan J. V. [3 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Psychol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Anesthesiol, NL-1105 AZ Amsterdam, Netherlands
[3] Erasmus MC, Dept Med Psychol & Psychotherapy, Rotterdam, Netherlands
[4] Leiden Univ, Med Ctr, Dept Psychiat, Leiden, Netherlands
[5] Riagg Rijnmond, Dept Psychotherapy, Schiedam, Netherlands
来源
PLOS ONE | 2012年 / 7卷 / 08期
关键词
COGNITIVE-BEHAVIORAL THERAPY; FUNCTIONAL SOMATIC SYMPTOMS; PRIMARY-CARE; PERSONALITY-DISORDERS; SOMATOFORM DISORDERS; GENERAL-PRACTITIONERS; HEALTH-CARE; DSM-III; SOMATIZATION DISORDER; MEDICAL-CARE;
D O I
10.1371/journal.pone.0042629
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:14
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