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 type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Beijing HuiLongGuan Hospital Academic / other |
| Locations | 1 site (Hefei, Anhui) |
| Status | Recruiting |
| Started | October 16, 2026 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | September 4, 2026 |
| Trial ID | NCT07805200 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
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The Fourth People's Hospital of Anhui Province
Hefei, Anhui, China Recruiting
Study contacts
- Study coordinator: Xiang-yang Zhang
- Email: zhangxy99@mail.tsinghua.edu.cn
- Phone: 18513299860
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.