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Bilateral rTMS for suicidal ideation in depression

Bilateral rTMS for suicidal ideation in depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039998
Enrollment
Unknown
Registered
2020-11-17
Start date
2020-11-23
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

depression

Interventions

treatment group:accelerate bilateral TBS
waiting group:accelerate bilateral TBS

Sponsors

Shenzhen Kangning Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. All the included patients met the diagnostic criteria for depressive episode in ICD-10, and it was the first episode; 2. A definite diagnosis of depressive episode by an attending psychiatrist and an associate chief psychiatrist; 3. The answer for the fourth or fifth item of Beck Suicidal Ideation Scale- Chinese version is "weak" or "moderate to strong"; 4. Age 18-65 years old, men and women are not limited, right-handed; 5. There were no contraindications to TMS in EEG; 6. No regular use of antidepressants, mood stabilizers, benzodiazepines, antipsychotics, rTMS or MECT, and no systematic psychotherapy within 2 weeks prior to inclusion; 7. Willing and informed consent to participate in this study.

Exclusion criteria

Exclusion criteria: 1.Exclude history of serious physical diseases, organic brain diseases and mental disorders caused by thyroid diseases or other physical diseases; 2.Exclude depression or psychogenic depression caused by other psychoactive substances or non-dependent substances, comorbidity compulsive disorder/schizophrenia/comorbidity borderline personality disorder/substance abuse or addiction, and history of hypomania/manic episodes; 3.Exclude patients with poor communication comprehension or cognitive impairment who cannot complete the psychological assessment, or who are difficult to complete the psychological assessment due to other reasons; 4.Patients with intracranial metal materials, pacemakers and stents, cataract lens replacement surgery, epilepsy risk, family history of epilepsy, pregnant and lactating women were excluded; 5.Excluding a history of suicide attempt, severe non-suicidal self-injuriou behavior, suicidal behavior in the waiting period, or unsuitability for further participation in this study due to illness or other reasons during the waiting period; 6.Those who have no intention to participate in this study and quit before rTMS are excluded.

Design outcomes

Primary

MeasureTime frame
Beck Scale for Suicide Ideation-Chinese Version;Hamilton's Depression Scale -24;

Countries

China

Contacts

Public ContactLingyun Zeng

Shenzhen Kangning Hospital

zly15222265@163.com+86 13924620714

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026