Effectiveness of psychosomatic therapy for patients with persistent somatic symptoms: Results from the CORPUS randomised controlled trial in primary care

被引:6
|
作者
Wortman, Margreet S. H. [1 ,2 ,5 ]
van der Wouden, Johannes C. [2 ]
Twisk, Jos W. R. [3 ]
Visser, Bart [1 ]
Assendelft, Willem J. J. [4 ]
van der Horst, Henriette E. [2 ]
Hartman, Tim C. Olde [4 ]
机构
[1] Amsterdam Univ Appl Sci, Fac Hlth, Ctr Expertise Urban Vital, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Amsterdam Publ Hlth Res Inst, Dept Gen Practice, Amsterdam UMC, De Boelelaan, NL-1117 Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Amsterdam Publ Hlth Res Inst, Dept Epidemiol & Data Sci, Amsterdam UMC, Amsterdam, Netherlands
[4] Radboud Univ Nijmegen, Radboud Inst Hlth Sci, Dept Primary & Commun Care, Med Ctr, Nijmegen, Netherlands
[5] Van der Boechorststr 7, NL-1081 BT Amsterdam, Netherlands
关键词
Clinical trial; Primary care; Persistent Somatic Symptoms (PSS); Psychosomatic therapy; MEDICALLY UNEXPLAINED SYMPTOMS; COGNITIVE-BEHAVIORAL THERAPY; SOMATOFORM DISORDERS; MOVEMENT CONTROL; BODILY DISTRESS; CHRONIC PAIN; PHYSIOTHERAPY; DISABILITY; MANAGEMENT; EXERCISE;
D O I
10.1016/j.jpsychores.2023.111178
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To evaluate the effectiveness of psychosomatic therapy versus care as usual in primary care for patients with persistent somatic symptoms (PSS).Methods: We conducted a pragmatic, two-armed, randomised controlled trial among primary care patients with PSS in the Netherlands that included 39 general practices and 34 psychosomatic therapists. The intervention, psychosomatic therapy, consisted of 6-12 sessions delivered by specialised exercise-and physiotherapists. Pri-mary outcome measure: patient's level of functioning. Secondary outcomes: severity of physical and psychosocial symptoms, health-related quality of life, health-related anxiety, illness behaviour and number of GP contacts.Results: Compared to usual care (n = 85), the intervention group (n = 84) showed no improvement in patient's level of functioning (mean difference -0.50 [95% CI-1.10 to 0.10]; p = .10), and improvement in health-related anxiety (mean difference -1.93 [95% CI-3.81 to-0.04]; p = .045), over 12 months. At 5-month follow-up, we found improvement in physical functioning, somatisation, and health-related anxiety. The 12-month follow-up revealed no therapy effects. Subgroup analyses showed an overall effect in patient's level of functioning for the group with moderate PSS (mean difference -0.91 [95% CI-1.78 to-0.03]; p = .042). In the year after the end of therapy, the number of GP contacts did not differ significantly between the two groups.Conclusion: We only found effects on some secondary outcome measures, and on our primary outcome measure especially in patients with moderate PSS, the psychosomatic therapy appears promising for further study.Trial registration: the trial is registered in the Netherlands Trial Registry, https://trialsearch.who.int/Trial2. aspx?TrialID=NTR7356 under ID NTR7356.
引用
收藏
页数:10
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