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Modulating Context Generalization Through Transcranial Direct Current Stimulation

Butler Hospital logo

Butler Hospital

Status

Withdrawn

Conditions

Anxiety and Fear

Treatments

Device: sham tDCS
Device: active tDCS

Study type

Interventional

Funder types

Other

Identifiers

NCT03374605
1705-002

Details and patient eligibility

About

Behavioral adaptation is particularly relevant to anxiety and related disorders, where exposure-based therapies rely on such adaptation as part of behavior therapy.. However, while initial fear reactions generalize easily across contexts, subsequent adaption of behavior through learning is context-specific. The primary goal of this study is to investigate whether transcranial direct current stimulation (tDCS) can be used to acutely impact generalization of subsequent learning across contexts in an experimental paradigm. As part of this study, participants will complete a clinical interview and questionnaires, as well as a computer task asking them to make choices between stimuli on the screen and during which they may or may not receive tDCS.

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Primary diagnosis of an anxiety or related disorder, (defined as panic disorder, social anxiety disorder, generalized anxiety disorder, obsessive-compulsive disorder, and/or post-traumatic stress disorder);
  2. aged 18-55;
  3. ability to speak, read, write, and understand English sufficiently well to complete study procedures and provide informed consent;
  4. Stable psychiatric medication use for at least 6 weeks.

Exclusion criteria

  1. Lifetime history of psychotic symptoms or bipolar disorder,
  2. Current substance use disorder;
  3. Acute suicidality or homicidality,
  4. Significant neurological disorder,
  5. Any problems that would interfere with study participation, significant or unstable medical disorders and tDCS-related contraindications (e.g., implanted metallic substances, pregnancy, holes in the skull, skin abnormalities under stimulation sites).

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Active tDCS
Experimental group
Treatment:
Device: active tDCS
Sham tDCS
Sham Comparator group
Treatment:
Device: sham tDCS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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