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Clinical Trials/NL-OMON45026
NL-OMON45026
Completed
Not Applicable

Transcranial Direct Current Stimulation as treatment for Auditory Hallucinations. A sham-controlled trial - tDCS as treatment for auditory hallucinations

niversitair Medisch Centrum Utrecht0 sites102 target enrollmentTBD
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Conditionspsychiatrische stoornissenauditory hallucinationshearing of voices

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
psychiatrische stoornissen
Sponsor
niversitair Medisch Centrum Utrecht
Enrollment
102
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
niversitair Medisch Centrum Utrecht

Eligibility Criteria

Inclusion Criteria

  • •\- Diagnosis of schizophrenia\-spectrum disorder, affective disorder, personality disorder, post\-traumatic stress disorder or hearing disorder.
  • •\- Age over 18
  • •\- Frequent auditory hallucinations (at least 5 times a week as indicated by the screening form).
  • •\- Patients are on a stable dose of antipsychotic medication (which can also be zero) for at least 2 weeks
  • •\- Mentally competent for informed consent.
  • •\- Provided written informed consent.

Exclusion Criteria

  • •\- Metal objects in or around the head that cannot be removed (i.e. cochlear implant, surgical clips, piercing)
  • •\- History of seizures
  • •\- History of eye trauma with a metal object or professional metal workers
  • •\- History of brain surgery, brain infarction, head trauma, cerebrovascular accident, broken skull, brain tumour, heart disease, cardiac pacemaker.
  • •\- Skin disease on the scalp on the position of the tDCS electrodes
  • •\- Coercive treatment based on a judicial ruling
  • •\- Pregnancy in female patients. A pregnancy test will be used in cases of doubt, e.g. females of childbearing age who are sexually active but do not use any form of contraceptives.
  • •\- Participation in TMS research in the previous 6 months
  • •\- Mentally incompetent.

Outcomes

Primary Outcomes

Not specified

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