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Effect of low-frequency rTMS on working memory in adolescent patients with major depressive disorder: a magnetic resonance imaging study

Effect of low-frequency rTMS on working memory in adolescent patients with major depressive disorder: a magnetic resonance imaging study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037878
Enrollment
Unknown
Registered
2020-09-03
Start date
2020-09-03
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Major depressive disorder

Interventions

Healthy control:None
True stimulation group:rTMS

Sponsors

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 17 Years

Inclusion criteria

Inclusion criteria: Patients group: 1. Provide informed consent; 2. The DSM-IV Axis I disorder was assessed by SCID, which met the diagnostic criteria of DSM-IV depression, and had never received any treatment; 3. HAMD-17 total score >= 17; 4. Aged 13-17 years, at least 6 years of education; 5. Han nationality, right handed; 6. Binocular naked vision or corrected visual acuity was normal. Healthy control group 1. The subjects or their relatives of the third generation of two lineages did not meet any diagnostic criteria of mental illness in DSM-IV, and were not related to the patients group; The other criteria were 2-6.

Exclusion criteria

Exclusion criteria: Patients group: 1. Patients with a history of severe physical or brain organic diseases and craniocerebral trauma; 2. Full scale intelligence quotient (FIQ <= 80) of WAIS-RC; 3. Patients with a history of drug, alcohol or other psychoactive substance abuse; 4. Patients with metal in the body, such as pacemaker; 5. Patients with contraindications to MRI or those who can't tolerate MRI scanning environment, such as claustrophobia. Healthy control group: the same as the patient group. The age, gender and years of education were matched with the patients group.

Design outcomes

Primary

MeasureTime frame
Effect;MRI;

Secondary

MeasureTime frame
Safety;Cogntion;

Countries

China

Contacts

Public ContactZheng Wei

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)

zhengwei0702@163.com+86 20-81268028

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026