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High-Definition Transcranial Direct Current Stimulation as a Treatment of Negative Symptoms of Schizophrenia

S

Shanghai Mental Health Center

Status

Terminated

Conditions

Schizophrenia

Treatments

Device: Sham HD-tDCS
Device: HD-tDCS

Study type

Interventional

Funder types

Other

Identifiers

NCT03602716
17411970000

Details and patient eligibility

About

In this study, investigators designed a double-blind randomized trial to prove a more reliable evidence to show how the treatment by using high-definition transcranial direct current stimulation (HD-tDCS) can relieve negative symptoms in patients with predominant negative symptoms of schizophrenia, especially on improving participants' anhedonia condition and social cognition, through stimulating the left dorsolateral prefrontal cortex (DLPFC). Participants will be divided into active and sham HD-tDCS groups equally.

Full description

Schizophrenia is one of the most disabling psychiatric disorders that almost 1% worldwide population suffer from this devastating illness. The clinical expression of this illness has been categorized into different dimensions, though most of the patients are well treated with antipsychotic medication, the negative symptom is still one of the very refractory symptoms. Emerging evidence shows that transcranial direct current stimulation (tDCS) is a promising treatment for schizophrenia negative symptoms, however, findings are still controversial. HD-tDCS can provide a more stable and accurate direct current comparing with traditional tDCS, which gives a hope to treat negative symptoms in a more reliable way.

An association between negative symptoms and grey matter reductions in the prefrontal cortex is found, moreover, even during rest, hypoactivity of the prefrontal cortex, particularly of the left dorsolateral, and of the anterior cingulate regions, has been linked to negative symptoms of schizophrenia. It has been observed that tDCS could relatively alleviate negative symptoms in patients with schizophrenia by stimulating the left DLPFC through an anodal electrode, which has been proved can also modulate brain functional connectivity and have clinical improvements.

Half of the participants with a clinical presentation of predominant negative symptoms will be stimulated by active HD-tDCS and the rest will have a sham stimulation. HD-tDCS is going to be delivered at 1.5 mA intensity for 20 minutes once a day; sessions will be performed on 10 days 5 consecutive weekdays with sustained effects at 1 (T2) and 3 (T3) months. A Soterix Medical 4x1 HD-tDCS will be used with the anode placed over the left DLPFC (F3), surrounded by four cathodal electrodes at F5, F1, FC3 and AF3, based on the 10/20 international EEG system. All the outcomes will be assessed at baseline (T0, before HD-tDCS sessions), one day after the 10th HD-tDCS sessions (T1), and also at T2 and T3. Both participants and investigators will be blind to this treatment.

Enrollment

12 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with diagnostic schizophrenia by DSM-IV
  • patients at an age between 18-60 years of Han nationality
    1. baseline score equal or higher than 4 in at least two items in negative symptoms at PANSS; 2) or baseline score equal or higher than 3 points in at least 1/3 items (including apathy) for negative symptoms; and 3)No more than 2 items have a score higher than 3 points for positive symptoms at PANSS.
  • willing to participate in the experiment and take treatment

Exclusion criteria

  • other psychiatric diagnoses
  • criteria for bipolar disorder; dementia; other psychotic disturbs; substance-related disorders
  • schizophrenia caused by organic diseases
  • other mental disorders caused by drugs and alcohol
  • IQ<70
  • presence of serious suicidal behaviour
  • claustrophobic or pregnancy
  • metal implantation in vivo
  • specific tDCS limitations (such as anatomic problems and high sensitivity on current)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

12 participants in 2 patient groups

HD-tDCS group
Experimental group
Description:
This HD-tDCS group will be stimulated by active HD-tDCS.
Treatment:
Device: HD-tDCS
Sham HD-tDCS group
Sham Comparator group
Description:
This sham HD-tDCS group will have a sham stimulation with HD-tDCS.
Treatment:
Device: Sham HD-tDCS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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