Repetitive transcranial magnetic stimulation for the treatment of negative symptoms in residual schizophrenia: rationale and design of a sham-controlled, randomized multicenter study

被引:22
作者
Cordes, Joachim [1 ]
Falkai, P. [2 ]
Guse, B. [2 ]
Hasan, A. [2 ]
Schneider-Axmann, T. [2 ]
Arends, M. [1 ]
Winterer, G. [1 ]
Woelwer, W. [1 ]
Ben Sliman, E. [1 ]
Ramacher, M. [1 ]
Schmidt-Kraepelin, C. [1 ]
Ohmann, C. [4 ]
Langguth, B. [3 ]
Landgrebe, M. [3 ]
Eichhammer, P. [3 ]
Frank, E. [3 ]
Burger, J. [3 ]
Hajak, G. [3 ]
Rietschel, M. [5 ]
Wobrock, T. [2 ]
机构
[1] Univ Dusseldorf, Dept Psychiat & Psychotherapy, D-40629 Dusseldorf, Germany
[2] Univ Gottingen, Dept Psychiat & Psychotherapy, Gottingen, Germany
[3] Univ Regensburg, Dept Psychiat & Psychotherapy, Regensburg, Germany
[4] Univ Dusseldorf, Coordinat Ctr Clin Trials, D-40629 Dusseldorf, Germany
[5] Cent Inst Mental Hlth, Dept Genet Epidemiol Psychiat, D-6800 Mannheim, Germany
关键词
Residual schizophrenia; Repetitive transcranial magnetic stimulation; Neurobiology; BIOLOGICAL-PSYCHIATRY WFSBP; HANS RATING-SCALE; DEPRESSION SCALE; WORLD-FEDERATION; CONTROLLED-TRIAL; BRAIN; GUIDELINES; SOCIETIES; TMS;
D O I
10.1007/s00406-009-0060-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Current meta-analysis revealed small, but significant effects of repetitive transcranial magnetic stimulation (rTMS) on negative symptoms in patients with schizophrenia. There is a need for further controlled, multicenter trials to assess the clinical efficacy of rTMS on negative symptoms in schizophrenia in a larger sample of patients. The objective of this multicenter, randomized, sham-controlled, rater- and patient-blind clinical trial is to investigate the efficacy of 3-week 10-Hz high frequency rTMS add on to antipsychotic therapy, 15 sessions per 3 weeks, 1,000 stimuli per session, stimulation intensity 110% of the individual motor threshold) of the left dorsolateral prefrontal cortex for treating negative symptoms in schizophrenia, and to evaluate the effect during a 12 weeks of follow-up. The primary efficacy endpoint is a reduction of negative symptoms as assessed by the negative sum score of the positive and negative symptom score (PANSS). A sample size of 63 in each group will have 80% power to detect an effect size of 0.50. Data analysis will be based on the intention to treat population. The study will be conducted at three university hospitals in Germany. This study will provide information about the efficacy of rTMS in the treatment of negative symptoms. In addition to psychopathology, other outcome measures such as neurocognition, social functioning, quality of life and neurobiological parameters will be assessed to investigate basic mechanisms of rTMS in schizophrenia. Main limitations of the trial are the potential influence of antipsychotic dosage changes and the difficulty to ensure adequate blinding.
引用
收藏
页码:189 / 197
页数:9
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