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New treatment option for Healthy Controls
Official title Temporal Interference Stimulation for Social Cognition
ClinicalTrials.gov ID: NCT06607432
What this study is testing
- What it's testing
- The long-term goal of this project is to evaluate whether a procedure termed transcranial interference stimulation (tIS) may be useful in the future in the treatment of severe neuropsychiatric disorders such as schizophrenia. The purpose of this stage of the project is to evaluate the safety and tolerability of tIS administration in healthy volunteers.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 55. Healthy volunteers may be eligible.
You may be able to join if
- Male or female
- Age 18-55 years
- Wechsler Adult Intelligence Scale (WAIS) intelligence quotient (IQ) \>70
- Competent and willing to sign informed consent.
- Shall not have been prescribed any standing medications for treatment of a Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition...
You likely can't join if
- Has a history of an illness, disease, condition injury, or disability which, in the opinion of the principal investigator (PI), may interfere with...
- Contraindication to MRI (e.g. metal implants, claustrophobia, pregnancy)
- On the Columbia-Suicide Severity Rating Scale (C-SSRS) Screen Version-Recent, answers YES to Question 3 and NO to Question 6 (Moderate Risk) or...
- Presence or positive history of significant medical illnesses, including high blood pressure(defined as systolic blood pressure (SBP) \>140 or...
- Women of childbearing potential who, at enrollment or during the study:
- have a positive urine pregnancy test or a self-reported pregnancy;
See the full eligibility criteria
- Male or female
- Age 18-55 years
- Wechsler Adult Intelligence Scale (WAIS) intelligence quotient (IQ) \>70
- Competent and willing to sign informed consent.
- Shall not have been prescribed any standing medications for treatment of a Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) Axis I psychiatric disorders within 90 days of the study and shall...
- Healthy relative to age-dependent expectation as determined by medical history and physical examination within 90 days of enrollment.
- Has a history of an illness, disease, condition injury, or disability which, in the opinion of the principal investigator (PI), may interfere with the completion of all study requirements per protocol, impact the...
- Contraindication to MRI (e.g. metal implants, claustrophobia, pregnancy)
- On the Columbia-Suicide Severity Rating Scale (C-SSRS) Screen Version-Recent, answers YES to Question 3 and NO to Question 6 (Moderate Risk) or answers YES to Question 4, 5, or 6 (High Risk).
- Presence or positive history of significant medical illnesses, including high blood pressure(defined as systolic blood pressure (SBP) \>140 or diastolic blood pressure (DBP) \>90, low blood pressure (SBP \ 20%), cardiac...
- Women of childbearing potential who, at enrollment or during the study:
- have a positive urine pregnancy test or a self-reported pregnancy;
- are heterosexually active without usage of a medically acceptable, highly effective contraceptive method\ ( 1% pregnancy rate); or
- are planning to become pregnant during the course of this study, as determined by the PI, are excluded from study participation. Examples include tubal ligation, vasectomized partner, intrauterine device (IUD) or...
The study team makes the final eligibility decision.
Where it's taking place
- New York, New York, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 55 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include New York, New York, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.