Centre Hospitalier Le Vinatier, PSYR2 team, Bat 416 - 1st floor; 95 boulevard Pinel, 69678, F-69500, Bron cedex, France.
INSERM, U1028; CNRS, UMR5292; Lyon Neuroscience Research Center, PSYR2 Team, F-69000, Lyon, France.
Trials. 2021 Dec 28;22(1):964. doi: 10.1186/s13063-021-05928-9.
One out of three patients with schizophrenia failed to respond adequately to antipsychotics and continue to experience debilitating symptoms such as auditory hallucinations and negative symptoms. The development of additional therapeutic approaches for these persistent symptoms constitutes a major goal for patients. Here, we develop a randomized-controlled trial testing the efficacy of high-frequency transcranial random noise stimulation (hf-tRNS) for the treatment of resistant/persistent symptoms of schizophrenia in patients with various profiles of symptoms, cognitive deficits and illness duration. We also aim to investigate the biological and cognitive effects of hf-tRNS and to identify the predictors of clinical response.
In a randomized, double-blind, 2-arm parallel-group, controlled, multicentre study, 144 patients with schizophrenia and persistent symptoms despite the prescription of at least one antipsychotic treatment will be randomly allocated to receive either active (n = 72) or sham (n = 72) hf-tRNS. hf-tRNS (100-500 Hz) will be delivered for 20 min with a current intensity of 2 mA and a 1-mA offset twice a day on 5 consecutive weekdays. The anode will be placed over the left dorsolateral prefrontal cortex and the cathode over the left temporoparietal junction. Patients' symptoms will be assessed prior to hf-tRNS (baseline), after the 10 sessions, and at 1-, 3- and 6-month follow-up. The primary outcome will be the number of responders defined as a reduction of at least 25% from the baseline scores on the Positive and Negative Syndrome Scale (PANSS) after the 10 sessions. Secondary outcomes will include brain activity and connectivity, source monitoring performances, social cognition, other clinical (including auditory hallucinations) and biological variables, and attitude toward treatment.
The results of this trial will constitute a first step toward establishing the usefulness of hf-tRNS in schizophrenia whatever the stage of the illness and the level of treatment resistance. We hypothesize a long-lasting effect of active hf-tRNS on the severity of schizophrenia symptoms as compared to sham. This trial will also have implications for the use of hf-tRNS as a preventive intervention of relapse in patients with schizophrenia.
ClinicalTrials.gov NCT02744989. Prospectively registered on 20 April 2016.
三分之一的精神分裂症患者对抗精神病药物反应不足,持续存在听力幻觉和阴性症状等使人虚弱的症状。为这些持续存在的症状开发额外的治疗方法是患者的主要目标。在这里,我们进行了一项随机对照试验,以测试高频经颅随机噪声刺激(hf-tRNS)治疗具有各种症状、认知缺陷和疾病持续时间特征的精神分裂症患者的难治性/持续性症状的疗效。我们还旨在研究 hf-tRNS 的生物学和认知效应,并确定临床反应的预测因素。
在一项随机、双盲、2 臂平行组、对照、多中心研究中,将 144 名精神分裂症患者和持续存在症状(尽管已开处至少一种抗精神病药物治疗)的患者随机分为接受活性(n = 72)或假(n = 72)hf-tRNS 治疗。hf-tRNS(100-500 Hz)将以 2 mA 的电流强度和 1 mA 的偏移每日两次共 5 个连续工作日每天 20 分钟。阳极置于左侧背外侧前额叶皮质,阴极置于左侧颞顶交界处。在 hf-tRNS 之前(基线)、治疗 10 次后以及 1、3 和 6 个月随访时评估患者的症状。主要结局是根据阳性和阴性症状量表(PANSS)的基线评分,在 10 次治疗后减少至少 25%的应答者数量。次要结局包括大脑活动和连通性、源监测表现、社会认知、其他临床(包括听力幻觉)和生物学变量以及对治疗的态度。
该试验的结果将是朝着确定 hf-tRNS 在精神分裂症中的有用性迈出的第一步,无论疾病阶段和治疗抵抗程度如何。我们假设与假刺激相比,活性 hf-tRNS 对精神分裂症症状的严重程度有持久的影响。该试验也将对 hf-tRNS 作为精神分裂症患者复发的预防干预措施的使用具有意义。
ClinicalTrials.gov NCT02744989。于 2016 年 4 月 20 日前瞻性注册。