Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 12:37 PM
Ignite Modification Date: 2025-12-24 @ 12:37 PM
NCT ID: NCT06134661
Eligibility Criteria: Inclusion Criteria: * 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 Criteria: * 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
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 60 Years
Study: NCT06134661
Study Brief:
Protocol Section: NCT06134661