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A comparative efficacy study of convulsion-free electroconvulsive shock and magnetic shock therapy to improve suicidal ideation and behavior

A comparative efficacy study of convulsion-free electroconvulsive shock and magnetic shock therapy to improve suicidal ideation and behavior

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091843
Enrollment
Unknown
Registered
2024-11-05
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

MDD with suicide

Interventions

MST group:none

Sponsors

the first hospital of hebei medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the Diagnostic and Statistical Manual of Mental Disorders (5th Edition) (DSM-5) MDD diagnosis (only patients with Article 9 suicidal thoughts or behaviors or plans at the time of diagnosis were included). 2.18-65 years old, gender is not limited. 3.Currently taking only a single antidepressant. 4.Can fully understand the matters of the questionnaire and the task requirements. 5.Volunteer to participate in this study and sign the relevant informed consent form.

Exclusion criteria

Exclusion criteria: 1. The presence of any other mental disorder as interviewed by the SCID-5-CV; 2. A history of serious physical illness, including cardiovascular and neurologic diseases, and traumatic brain injury; 3. A history of epilepsy; 4. An inability to cooperate in completing the scales; 5.Missing or imperfect data on the baseline information, and on each of the rating scales.

Design outcomes

Primary

MeasureTime frame
Beck scale for suicide ideation,Self-rating Idea of Suicide Scale,Columbia-Suicide Severity Rating Scale;

Countries

China

Contacts

Public ContactWang Ran

the first hospital of hebei medical university

wangran104@hptmail.com+86 15633834532

Outcome results

None listed

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