Actively Recruiting

Phase Not Applicable
Age: 15Years - 25Years
All Genders
Healthy Volunteers
NCT07397858

Cognition and Behavior With Sham Accelerated TMS

Led by University of California, Davis · Updated on 2026-05-06

25

Participants Needed

1

Research Sites

90 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical study is to understand how a person's expectations about treatment can influence their mood, motivation, and reactions to everyday rewards. The study includes young people ages 15-25 who will complete a sham (placebo) version of an accelerated transcranial magnetic stimulation (TMS) treatment. No active brain stimulation is given. The main questions this study aims to answer are: 1. Do expectancy and treatment beliefs change during and after an accelerated sham TMS schedule? 2. Do these expectations influence mood, reward processing, or craving? 3. Does a more intensive schedule of sham sessions lead to different expectancy effects than a slower, once-daily schedule? Participants will: * Complete baseline clinical assessments and an MRI session * Undergo five days of accelerated sham TMS (no active brain stimulation is delivered) * Complete post-treatment MRI and follow-up assessments at 1 week and 4 weeks

CONDITIONS

Official Title

Cognition and Behavior With Sham Accelerated TMS

Who Can Participate

Age: 15Years - 25Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • English speaking
  • Able to provide informed consent (and assent if < 18 years)
  • 15-25 years old
Not Eligible

You will not qualify if you...

  • Unable to consent due to medical condition, psychosis, substance use, etc
  • Acute suicidal crisis or active medical illness interfering with participation
  • Contraindications to MRI such as metal in the body, surgical clips, metal fragments in eyes, non-removable piercings, braces, or permanent retainers
  • Major neurological problems including seizure disorder, traumatic brain injury with loss of consciousness, or sensory impairments like blindness
  • Participation in any clinical study involving investigational treatment within previous 30 days or plans for concurrent participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UC Davis Medical Center

Sacramento, California, United States, 95817

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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