Status:

TERMINATED

Accelerated rTMS for Psychomotor Slowing

Lead Sponsor:

University of Bern

Conditions:

Schizophrenia; Psychosis

Schizophrenia and Related Disorders

Eligibility:

All Genders

18-60 years

Phase:

NA

Brief Summary

The goal of this clinical trial is to optimize the treatment of psychomotor slowing in patients with schizophrenia using Transcranial Magnetic Stimulation (TMS). A previous randomized controlled trial...

Detailed Description

Schizophrenia is a chronic disorder causing tremendous burden to the patients, families, and society. Besides prominent symptoms such as hallucinations, delusions, and thought disorder, the majority o...

Eligibility Criteria

Inclusion

  • 18-60 years.
  • Ability and willingness to participate in the study
  • Ability to provide written informed consent
  • Informed Consent as documented by signature (Appendix Informed Consent Form)
  • Schizophrenia spectrum disorders according to DSM-5 with psychomotor slowing (SRRS score ≥ 15).

Exclusion

  • Substance abuse or dependence other than nicotine.
  • Past or current medical or neurological conditions associated with impaired or aberrant movement, such as brain tumors, stroke, M. Parkinson, M. Huntington, dystonia.
  • Severe head trauma with subsequent loss of consciousness.
  • Epilepsy or other convulsions.
  • History of any hearing problems or ringing in the ears.
  • Standard exclusion criteria for TMS (implanted electronic devices (e.g. pacemakers, implantable cardioverter-defibrillators, vagus nerve stimulators and wearable cardioverter-defibrillators, ocular implants, deep brain stimulators, implanted medication pumps, intracardiac lines even when removed) and/or conductive objects near the coil (e.g. cochlear implants, implanted electrodes/stimulators, aneurysm clips or coils, stents and bullet fragments)
  • Women who are pregnant or breastfeeding.
  • Any TMS treatment in the past 2 months.
  • If applicable: standard exclusion criteria for MRI (study participation without MRI is possible)
  • Intention to become pregnant during the course of the study
  • Previous enrolment into the current study
  • Enrolment of the investigator, his/her family members, employees, and other dependent persons

Key Trial Info

Start Date :

September 22 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 30 2024

Estimated Enrollment :

25 Patients enrolled

Trial Details

Trial ID

NCT06134661

Start Date

September 22 2023

End Date

August 30 2024

Last Update

September 25 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University Hospital of Psychiatry and Psychotherapy

Bern, Switzerland, 3000