Skip to content

Study on the efficacy of iTBS targeting NAc and sgACC in regulating the reward circuit function to improve anhedonia in depression

Study on the efficacy of iTBS targeting NAc and sgACC in regulating the reward circuit function to improve anhedonia in depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125718
Enrollment
Unknown
Registered
2026-05-29
Start date
2026-05-29
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression with anhedonia features

Interventions

Group C:Single-target iTBS 2
Group A:Dual-target iTBS
Group B:Single-target iTBS 1
Group D:Sham iTBS (dual targets)

Sponsors

The Second Xiangya Hospital of Central South Univercity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 45 years old, Han ethnicity, right-handed; 2. Diagnosed by at least two psychiatrists, meeting the diagnostic criteria for Major Depressive Disorder (MDD) as per the 5th Edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM5), with a MADRS score of >= 20 or an HAMD-17 score of >= 17; 3. Evaluated by psychiatrists as having significant anhedonia symptoms, and meeting the standards on two anhedonia self-assessment scales, the score of the Shyness-Hamilton Anhedonia Scale - Chinese Version (SHAPS-C) is >= 20 and the score of the Chinese Version of the Pleasant Emotion Experience Scale (TEPS-C) is <= 76; 4. The types and doses of medication remained unchanged during the 4 weeks before treatment and throughout the entire study period; 5. The score of item 10 of the MADRS is <= 4.

Exclusion criteria

Exclusion criteria: 1.A history of epilepsy, seizures, stroke, or other serious organic brain diseases; 2.Presence of severe infectious diseases, malignant tumors, or other major unstable medical conditions; 3.Intellectual disability or developmental delay, presence of psychotic symptoms, or meeting the diagnostic criteria for other psychiatric disorders; 4.A history of substance abuse or psychoactive substance use; 5.Presence of intracranial implants (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes), or any other metallic objects in or near the head that cannot be safely removed (excluding dental fillings); 6.Contraindications to MRI or structural intracranial abnormalities detected on MRI; 7.Pregnant or breastfeeding women; 8.Receipt of electroconvulsive therapy (ECT) within the past 6 months, or transcranial magnetic stimulation (TMS) within the past 3 months; 9.Current daily use of lorazepam > 2 mg (or an equivalent dose), or use of antiepileptic drugs at any dose; 10.Presence of strong suicidal ideation, or a MADRS item 10 score > 4.

Design outcomes

Primary

MeasureTime frame
Chansges of MARDS scores;Changes of TEPS-C scores;Changes of brain functions;

Secondary

MeasureTime frame
Changes of HAMD-17 and SHAPS scores;Cognition evaluation;

Countries

China

Contacts

Public ContactYangpan Ou;Wenbin Guo

The Second Xiangya Hospital of Central South Univercity

ouyangpan33@csu.edu.cn+86 731 8529 2158

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026