Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Targeted brain stimulation for OCD: test of tTIS on nucleus accumbens

Official title: Individualized Targeted Transcranial Temporal Interference Stimulation for for Patients With Obsessive-Compulsive Disorders: A Double-Blinded, Randomized Controlled Trial

Run by Beijing HuiLongGuan Hospital · NCT07805200 · Data updated 2026-11-12

This study tests whether targeted temporal interference stimulation of the nucleus accumbens can help reduce obsessive-compulsive symptoms in adults with OCD, compared with sham stimulation.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment80 (estimated)
SponsorBeijing HuiLongGuan Hospital
Academic / other
Locations1 site (Hefei, Anhui)
StatusRecruiting
StartedOctober 16, 2026
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedSeptember 4, 2026
Trial IDNCT07805200 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–65 with a clinician-confirmed OCD diagnosis who can complete on-site assessments.

Probably not a fit

Individuals with certain comorbid psychiatric conditions, recent neurostimulation exposure, or MRI/tTIS contraindications may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial evaluates the therapeutic potential and possible brain-behavior mechanisms of nucleus accumbens–targeted transcranial temporal interference stimulation (tTIS) in OCD. Participants receive either active or sham tTIS for 5 consecutive days, with outcomes measured at baseline, after treatment, and during follow-up. Assessments include the Yale-Brown Obsessive Compulsive Scale, psychological questionnaires, behavioral tasks, resting-state EEG, and multimodal MRI to explore clinical effects and neural changes associated with the intervention.

Why it matters

Potential benefit: If successful, patients could experience a reduction in OCD symptoms and new insights into brain mechanisms behind OCD and stimulation-based therapies.

How similar studies have gone: Prior brain stimulation approaches for OCD have shown variable benefits; this study tests a novel NAc-targeted tTIS approach with exploratory neuroimaging.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Were between 18 and 65 years old;
* Were diagnosed with OCD by an experienced psychiatrist utilizing the Structured Clinical Interview for DSM-5 (SCID);
* Were able to participate in the entire trial and face-to-face on-site assessment

Exclusion Criteria:

* Pregnant or breastfeeding;
* Suffered from organic brain diseases or severe physical illness;
* Had a history of substance or alcohol abuse;
* Presence of comorbid psychiatric disorders (e.g., major depressive disorder) or a high risk of suicide;
* Have received electroconvulsive therapy, transcranial magnetic stimulation, tDCS, tACS, or other neurostimulation treatments within the past 6 months;
* Presence of contraindications to MRI or tTIS, such as severe head trauma, prior brain surgery, intracranial or cardiac metallic implants, etc.

Where it's running

  • The Fourth People's Hospital of Anhui Province
    Hefei, Anhui, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.