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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:
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.
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