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NCT02739347 · ClinicalTrials.gov registry record · NA

Non-Invasive Direct Current Stimulation for Cognition in Schizophrenia

A NA study, sponsored by Baylor College of Medicine.

Terminated
Registry status
NA
Development phase
17
Enrollment target

NCT02739347: Clinical Trial NA study, sponsored by Baylor College of Medicine.

NCT02739347 is a NA study that was terminated before completion, run by Baylor College of Medicine. The registered enrollment target is 17 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02739347, a NA study, was terminated before completion, sponsored by Baylor College of Medicine.

TERMINATED
Registry status
NA
Development phase
17 participants
Enrollment target

Study Summary

This study proposes to assess the effect of trans-cranial direct current stimulation (tDCS) on cognitive control, working memory, functional, clinical, and cognitive outcomes in schizophrenia patients.

Primary Outcome

The investigators will assess cognitive control using the Preparing to Overcome Prepotency (POP) task. The accuracy mean differences between the high and low control conditions will be used as dependent measures. The study is powered at 0.8 to observe a post-pre treatment improvement in cognitive control with a substantial effect size (d=0.56) compared to sham stimulation with effects relatively stable measured 2 months after baseline. The hypothesized effect size will be d=0.60.

Interventions

  • DEVICE Active Trans-cranial direct-current stimulation
  • DEVICE Sham Trans-cranial direct current stimulation

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2016-05
Est. Completion 2019-06
Phase NA
Baylor College of Medicine

616 total trials

Why NCT02739347 stopped before completion

NCT02739347 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Active Trans-cranial direct-current stimulation is the first listed.

NCT02739347 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02739347 about?

NCT02739347 is a clinical study titled "Non-Invasive Direct Current Stimulation for Cognition in Schizophrenia". This study proposes to assess the effect of trans-cranial direct current stimulation (tDCS) on cognitive control, working memory, functional, clinical, and cognitive outcomes in schizophrenia patients.

What is the current status of trial NCT02739347?

This trial is currently terminated. It is a NA study. The enrollment target is 17 participants. The study started on 2016-05. Estimated completion is 2019-06.

What interventions are being tested in trial NCT02739347?

The interventions under investigation include: Active Trans-cranial direct-current stimulation (DEVICE), Sham Trans-cranial direct current stimulation (DEVICE).

Who is sponsoring clinical trial NCT02739347?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02739347's enrollment target sits among peer trials

17 1871st of 2000 higher than 130 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02739347, the US trial registry maintained by the National Library of Medicine. NCT02739347 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.