Tailored care for somatoform vertigo/dizziness: study protocol for a randomised controlled trial evaluating integrative group psychotherapy

被引:10
|
作者
Lahmann, Claas [1 ,2 ]
Henningsen, P. [1 ,2 ]
Dieterich, M. [2 ,3 ,4 ]
Radziej, K. [1 ,2 ]
Schmid, G. [1 ,2 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Psychosomat Med & Psychotherapy, D-81675 Munich, Germany
[2] Univ Munich, Klinikum Grosshadern, German Integrated Ctr Res & Treatment Vertigo Bal, D-81377 Munich, Germany
[3] Univ Munich, Klinikum Grosshadern, Dept Neurol, D-81377 Munich, Germany
[4] SyNergy, Munich Cluster Syst Neurol, D-81377 Munich, Germany
关键词
Dizziness; Vertigo; Somatoform disorder; RCT; Psychotherapy; PHOBIC POSTURAL VERTIGO; QUALITY-OF-LIFE; PSYCHIATRIC-DISORDERS; DIZZINESS; SYMPTOMS; VALIDATION; DEPRESSION; MANAGEMENT; VALIDITY; THERAPY;
D O I
10.1007/s00415-015-7784-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Vertigo/dizziness (VD) ranks high in lifetime prevalence and clinical relevance. Nearly half of the complex VD disorders presenting at specialised units for vertigo or otoneurological disorders are not fully explained by an identifiable medical illness, but instead are related to anxiety, depressive, or somatoform disorders. Although there is some evidence that psychotherapy may be effective for these patients, therapeutic options remain unsatisfactory. This report describes the objectives, design and methods of a randomised, controlled clinical trial, evaluating the efficacy of manualised, multimodal group psychotherapy, based on integrative psychotherapy (IPT) and tailored to subgroups of mental disorders in medically unexplained VD. This psychotherapeutic approach will be compared to self-help groups (n = 172; n = 86 per study arm). Improvements with regard to handicap due to VD at 12 months follow-up will serve as primary outcome. Additionally, measures of generic quality of life, severity of vertigo, depression, anxiety, somatisation as well as Head Impulse Test and Computerized Static Posturography will be applied. We will also analyse the cost-effectiveness of this trial. The study aims to improve treatment of this therapeutically underserved population who are often severely impaired in their working and daily lives. Trial Registration: ClinicalTrials.gov Identifier: NCT02320851. Trial Status: This is an on-going study; recruitment for the study is about to start.
引用
收藏
页码:1867 / 1875
页数:9
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