Journal Article

Examining transcranial random noise stimulation as an add-on treatment for persistent symptoms in schizophrenia (STIM’Zo): a study protocol for a multicentre, double-blind, randomized sham-controlled clinical trial

Brunelin, Jerome, Llorca, Pierre Michel, Mondino, Marine, Poulet, Emmanuel, Fakra, Eric, Chupin, Marie, Schott-Pethelaz, Anne Marie, Attal, Jerome, Jardri, Renaud, Suaud-Chagny, Marie-Françoise, Haesebaert, Julie, Galvao, Filipe, Dollfus, Sonia, Plaze, Marion, El-Hage, Wissam, Magaud, Laurent, Benoit, Michel, Szekely, David

2021

Overview

Background 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. Methods 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. Discussion 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. Trial registration ClinicalTrials.gov NCT02744989. Prospectively registered on 20 April 2016

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Antipsychotics / Attitudes / Biomedicine / Brain research / Brain stimulation / Care and treatment / Clinical outcomes / Clinical trials / Diagnosis / Dorsolateral Prefrontal Cortex / Double-Blind Method / Double-blind studies / Hallucination / Hallucinations / Hallucinations - diagnosis / Hallucinations - therapy / Health Sciences / Human health and pathology / Humans / Innovations / Life Sciences / Magnetic resonance imaging / Medical imaging / Medicine / Medicine & Public Health / Mental depression / Methods / Multicenter Studies as Topic / Negative symptoms / Neoplasm Recurrence, Local / Neuroimaging / Neurosciences / Noninvasive brain stimulation / Psychiatrics and mental health / Psychotropic drugs / Quality of life / Randomized Controlled Trials as Topic / Schizophrenia / Schizophrenia - diagnosis / Schizophrenia - drug therapy / Statistics for Life Sciences / Study Protocol / tDCS / Testing / Transcranial Direct Current Stimulation / Treatment Outcome / Treatment resistance / tRNS