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Improving Cognition in Schizophrenia Using tDCS (ICDC)

Primary Purpose

Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
tDCS
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnostic and Statistical Manual of Mental Disorders (DSM)-V Diagnosis of Schizophrenia
  • Must understand spoken English sufficiently to comprehend testing procedures
  • Estimated premorbid intelligence quotient (IQ) > 70 (based on reading ability)
  • Ongoing care of a Psychiatrist, Psychologist, or other qualified mental health professional

Exclusion Criteria:

  • Metal in cranium
  • Cardiac lines/pacemaker
  • Medication pump
  • Increased intracranial pressure
  • Lifetime history of serious head injury (LOC > 1 hr.)
  • Sedatives or Benzodiazepines within 12 hours of testing
  • Clinically significant neurological disease (e.g., seizures)
  • History of mental retardation or developmental disability
  • Alcohol or substance dependence in the last 6 months
  • Alcohol or substance abuse in the last 1 month
  • Change in medication in past 6 weeks
  • Change in in living situation in the last 2 months
  • Inpatient hospitalization in past 3 months
  • Participation in prior studies involving tDCS

Sites / Locations

  • UCLA Semel Institute for Neuroscience and Human Behavior

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Sham Comparator

Arm Label

tDCS anodal stimulation

tDCS cathodal stimulation

Sham stimulation

Arm Description

anodal stimulation

cathodal stimulation

Sham stimulation. Termination of electrical stimulation following 30 seconds

Outcomes

Primary Outcome Measures

Change From Baseline in Cognition on MCCB
Summary score of the cognitive domains on the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB). Four nonsocial neurocognitive tasks were included: speed of processing, working memory, verbal memory, and reasoning/problem solving. Normed T-scores were calculated for each cognitive subdomain, as well as the cognitive composite score consisting of the average across the four subdomains. The T-scores have a mean of 50, with a difference of 10 points from the mean equaling one standard deviation. Higher T-scores are indicative of higher cognition.
Change From Baseline in Managing Emotions on MSCEIT
Total score on the Managing Emotions component of Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) The test consists of 141 items and 8 ability subtests, which assess four components of emotional processing. In this study, only branches 1 and 4 were administered, focusing on the Managing Emotions component. The total score reflects mean performance across the branches. The scores were converted to normed T-scores that have a mean of 50, with a difference of 10 points from the mean equaling one standard deviation. Higher T-scores are indicative of better performance.

Secondary Outcome Measures

Full Information

First Posted
August 26, 2015
Last Updated
February 6, 2018
Sponsor
University of California, Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT02539797
Brief Title
Improving Cognition in Schizophrenia Using tDCS
Acronym
ICDC
Official Title
Improving Cognition in Schizophrenia Using Transcranial Direct Current Stimulation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
October 2014 (Actual)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the benefits of transcranial direct current stimulation (tDCS), a new tool that is being developed as a safe and non-invasive neurostimulation method, for improving neurocognitive and social cognitive functions in schizophrenia. This procedure is non-invasive and painless and it results in increase or decrease of spontaneous neuronal firing in the brain. Its safety and beneficial effect on cognition has been demonstrated in healthy individuals and several clinical populations. In this pilot study, the investigators will examine the effect of tDCS on cognitive functions in 40 individuals with schizophrenia. Each participant will arrive for three visits, with approximately one week between each visit. During the first visit, participants will be interviewed about their psychiatric symptoms, personal life experiences, and emotional well being by a specially-trained interviewer. On each of the three visits, participants will receive one of three stimulations: a type of tDCS designed to increase neuronal firing, an alternative form of tDCS designed to decrease neuronal firing, and a sham tDCS (stimulation with no current). Immediately following the stimulation, participants will be asked to complete measures of mental abilities, including tests presented on a computer screen and paper-and-pencil tests. During each visit, participants will also undergo a standard measure of brain activity (EEG) while listening to tones. The first visit will last approximately five hours, and the other two visits will last approximately four hours each. The project will take approximately two years to complete.
Detailed Description
The investigators plan to recruit 40 individuals diagnosed with Schizophrenia. Participants will range from 18-55 years old. We will select stable, medicated patients who have not been hospitalized nor had any changes in their antipsychotic medications during the previous two months. Participants will not be tested within 12 hours of taking medications that may affect cognition (such as benzodiazepines and anticholinergics). All medications will be recorded. The investigators expect most of the patients to be relatively chronic (mean illness chronicity approximately 15 years, based on previous studies), although we will not select for chronicity. All participants will provide written informed consent after receiving a full explanation of the procedures according to approvals by the Institutional Review Boards. They will arrive for three visits. In the first visit, they will be consented, complete the diagnostic interview, the rating scales, and will undergo one of three randomly assigned stimulation conditions: 1) anodal tDCS, 2) cathodaltDCS, and 3) sham stimulation. They will also undergo an electroencephalography (EEG) procedure, in order to more directly assess the effect of tDCS on brain function. This visit will take approximately five hours to complete, and breaks will be given as needed. Immediately following stimulation, participants will complete neurocognitive, social cognitive, and EEG measures. There will be two 20-minute stimulation sessions, with a break of one hour between the sessions. After each session, participants will be asked to complete a portion of the basic cognitive, social cognitive, and EEG measures, so that half of the measures will be completed after the first 20 minute stimulation session and the other half will be completed after the second 20 minute stimulation session. The order of administration of the neurocognitive, social cognitive, and EEG measures will be randomized across participants within each group. During the second and third visits, participants will undergo the remaining two stimulation conditions, one randomly assigned condition each visit. These visits will take approximately four hours to complete, and each visit will be separated by at least one week from the previous visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
tDCS anodal stimulation
Arm Type
Experimental
Arm Description
anodal stimulation
Arm Title
tDCS cathodal stimulation
Arm Type
Active Comparator
Arm Description
cathodal stimulation
Arm Title
Sham stimulation
Arm Type
Sham Comparator
Arm Description
Sham stimulation. Termination of electrical stimulation following 30 seconds
Intervention Type
Device
Intervention Name(s)
tDCS
Intervention Description
comparing anodal, cathodal, and sham tDCS
Primary Outcome Measure Information:
Title
Change From Baseline in Cognition on MCCB
Description
Summary score of the cognitive domains on the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB). Four nonsocial neurocognitive tasks were included: speed of processing, working memory, verbal memory, and reasoning/problem solving. Normed T-scores were calculated for each cognitive subdomain, as well as the cognitive composite score consisting of the average across the four subdomains. The T-scores have a mean of 50, with a difference of 10 points from the mean equaling one standard deviation. Higher T-scores are indicative of higher cognition.
Time Frame
baseline and 20 minutes
Title
Change From Baseline in Managing Emotions on MSCEIT
Description
Total score on the Managing Emotions component of Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) The test consists of 141 items and 8 ability subtests, which assess four components of emotional processing. In this study, only branches 1 and 4 were administered, focusing on the Managing Emotions component. The total score reflects mean performance across the branches. The scores were converted to normed T-scores that have a mean of 50, with a difference of 10 points from the mean equaling one standard deviation. Higher T-scores are indicative of better performance.
Time Frame
baseline and 20 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnostic and Statistical Manual of Mental Disorders (DSM)-V Diagnosis of Schizophrenia Must understand spoken English sufficiently to comprehend testing procedures Estimated premorbid intelligence quotient (IQ) > 70 (based on reading ability) Ongoing care of a Psychiatrist, Psychologist, or other qualified mental health professional Exclusion Criteria: Metal in cranium Cardiac lines/pacemaker Medication pump Increased intracranial pressure Lifetime history of serious head injury (LOC > 1 hr.) Sedatives or Benzodiazepines within 12 hours of testing Clinically significant neurological disease (e.g., seizures) History of mental retardation or developmental disability Alcohol or substance dependence in the last 6 months Alcohol or substance abuse in the last 1 month Change in medication in past 6 weeks Change in in living situation in the last 2 months Inpatient hospitalization in past 3 months Participation in prior studies involving tDCS
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuri Rassovsky, PhD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Semel Institute for Neuroscience and Human Behavior
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29734347
Citation
Rassovsky Y, Dunn W, Wynn JK, Wu AD, Iacoboni M, Hellemann G, Green MF. Single transcranial direct current stimulation in schizophrenia: Randomized, cross-over study of neurocognition, social cognition, ERPs, and side effects. PLoS One. 2018 May 7;13(5):e0197023. doi: 10.1371/journal.pone.0197023. eCollection 2018.
Results Reference
derived

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Improving Cognition in Schizophrenia Using tDCS

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