ArticleThe Journal of clinical psychiatry2020
Transcranial Direct Current Stimulation for Negative Symptoms of Schizophrenia: Why the Reader Must Choose a Clinically Relevant Outcome.
Article in The Journal of clinical psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
- Efficacy and EEG-ECG mechanisms of taVNS combined with TEAS for negative symptoms of schizophrenia: a protocol for a 2 × 2 factorial randomized controlled trial.European archives of psychiatry and clinical neuroscience · 2026Article
Corrections and comments
- Comment on
Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A recent, large, randomized controlled trial (RCT) of 10 twice-daily sessions of active vs sham transcranial direct current stimulation (tDCS), delivered across 5 consecutive days to schizophrenia patients with high negative symptom burden, found that active treatment was superior to sham treatment by a mean of 2.65 points on the Positive and Negative Syndrome Scale, negative subscale (PANSS-N), at 6 weeks. This was the primary endpoint of the study. Because a difference of 2.65 PANSS-N points between the average active vs sham tDCS patient is a very small advantage, it appears that the finding was statistically but not clinically significant; why this is so is explained in the context of how the PANSS-N is scored. The study also found that, with response defined as 20% attenuation of PANSS-N scores, significantly more (40% vs 4%) active than sham group patients responded at 6 weeks. This was one of many secondary outcomes that the study examined. Because response is a clinically important endpoint, it appears that the finding was clinically as well as statistically significant; why this is so is also explained in the context of PANSS-N scoring. As a final poser, whereas the advantage for active tDCS for both outcomes persisted at 12 weeks, at neither 6 nor 12 weeks was active treatment superior to sham treatment on a global measure of functioning; this suggests that the advantage for active tDCS does not translate into real-life gains. The reader is provided with an understanding of how to critically read a paper that describes an RCT; of how to interpret a continuous outcome measure that describes the average patient versus a categorical outcome measure that describes a clinically important outcome in an entire group; and, most important of all, of the need to choose an outcome that is relevant to clinical practice.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.