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Cognitive Control of Negative Stimuli in BPD

Effects of Transcranial Direct Current Stimulation on the Cognitive Control of Negative Stimuli in Borderline Personality Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03636139
Enrollment
100
Registered
2018-08-17
Start date
2016-01-31
Completion date
2017-06-30
Last updated
2024-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Borderline Personality Disorder

Brief summary

Borderline personality disorder (BPD) is characterized by impairments in the cognitive control of negative information. These impairments in cognitive control are presumably due to blunted activity of the dorsolateral prefrontal cortex (dlPFC) along with enhanced activations of the limbic system. However, the impact of an excitatory stimulation of the dlPFC still needs to be elucidated. In the present study, we therefore assigned 50 patients with BPD and 50 healthy controls to receive either anodal or sham stimulation of the right dlPFC in a double-blind, randomized, between-subjects design.

Interventions

DEVICEtranscranial DC stimulation : anodal

anodal stimulation of the right dlPFC (i.e. F4) for 20 minutes

DEVICEtranscranial DC stimulation : sham

sham stimulation of the right dlPFC (i.e. F4) for 20 minutes

Sponsors

Freie Universität Berlin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Borderline Personality Disorder: * Diagnosis of borderline personality disorder

Exclusion criteria

Borderline Personality Disorder: * Diagnosis of current or previous bipolar disorder * Diagnosis of current substance dependency * Diagnosis of current major depression * Diagnosis of current or previous neurological disorders (e.g., epilepsy) * Tattoos or scarred skin on the left shoulder or scalp (i.e. F4) Inclusion Criteria Control Participants: * No current or previous diagnosis of a mental disorder

Design outcomes

Primary

MeasureTime frameDescription
Response latenciesResponse latencies were exclusively measured during the assigned interventions, which lasted approx. 20 minutes. No further time points were assessed.Response latencies were measured in the context of a delayed working memory task. In this paradigm, each trial started with a fixation cross (1000 ms), followed by the presentation of six target letters (1500 ms), which participants were asked to memorize. After a variable distracter period (i.e., interference duration of 1000, 2000, or 4000 ms), participants were presented a recognition display (until a response was made) and had to decide whether the presented letter was part of the initial set of letters. In half of the trials, the recognition display contained a previously presented target. The distracter period of the experimental paradigm was manipulated with regard to the factors valence (grey background screen, or neutral, or negative stimuli) and interference duration (1000, 2000, or 4000 ms). Neutral and negative affective stimuli were selected from the International Affective Picture System.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026