Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06540300
Status:
ENROLLING_BY_INVITATION
Last Update Posted:
None
First Post:
2024-07-10
Brief Title:
Effects of Repetitive Transcrannial Magnetic Stimulation on Non-Suicidal Self-Injury
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effects of Repetitive Transcrannial Magnetic Stimulation on Non-Suicidal Self-Injury
Status:
ENROLLING_BY_INVITATION
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Non-suicidal self-injury NSSI refers to a series of direct and consequently repeated injuries to ones body without suicidal intent At present it has become an important issue of mental disorders This article focuses on the formation mechanism of NSSI and the intervention effect of rTMS on NSSI patients At the same time NSSI patients are collected a treatment plan is designed to complete a two-week treatment and the results are analyzed The aim is to provide theoretical basis for the clinical diagnosis and treatment of NSSI and also to provide reference for the clinical diagnosis and treatment of NSSI patients
Detailed Description:
Research Objective Non suicidal self injury NSSI behavior is a common behavioral issue in psychiatric and psychiatric clinics Studies have shown that NSSI is on the rise in China and has become an important mental health issue Non suicidal self injury and suicide have similar clinical manifestations Therefore this study will intervene in the treatment of NSSI patients understand the occurrence of NSSI in psychiatric outpatient and inpatient wards and observe the efficacy of repeated transcranial magnetic stimulation intervention in NSSI patients in order to explore the current occurrence status and biopsychological etiology of NSSI in psychiatric clinical practice
Research Process If you agree to participate in this study please read and sign this informed consent form before participating in any of the following procedures
Research location All research processes and evaluation interviews were conducted at the Affiliated Brain Hospital of Nanjing Medical University
Study participants Participants clinically diagnosed with non suicidal self injury participated in this study aged 10-60 years regardless of gender All participants entered the study after signing the informed consent form
Research Procedures This study first clarifies your diagnosis by conducting interviews to understand your physical health status course of illness family history previous medical treatment and examination results We will assign a number to each participant establish a medical record and then perform corresponding psychological assessments magnetic resonance imaging examinations and repeat transcranial magnetic stimulation therapy for two weeks a total of 10 times
Possible Benefits All clinical scale evaluations imaging examinations and repeated transcranial magnetic stimulation interventions related to the study are free of charge Your research doctors and evaluators will conduct timely clinical observations of changes in your condition and provide you with systematic research follow-up and evaluation These evaluations will help make reasonable judgments about your disease status and treatment effectiveness and thus guide treatment decisions more scientifically In addition free treatment with repeated transcranial magnetic stimulation is also beneficial for the improvement of your condition The research team will coordinate with relevant staff in the hospital and department where you are seeking medical treatment to provide convenience in basic clinical services such as doctor appointments registration and waiting in order to save your visit time
Privacy and Confidentiality Issues If you decide to participate in this study your participation in the experiment and your personal information during the experiment will be kept confidential Responsible research doctors and other researchers will use your medical information for research but will not disclose your personal information If you are harmed by participating in this study you can receive free treatment andor corresponding compensation
Research Process If you agree to participate in this study please read and sign this informed consent form before participating in any of the following procedures
Research location All research processes and evaluation interviews were conducted at the Affiliated Brain Hospital of Nanjing Medical University
Study participants Participants clinically diagnosed with non suicidal self injury participated in this study aged 10-60 years regardless of gender All participants entered the study after signing the informed consent form
Research Procedures This study first clarifies your diagnosis by conducting interviews to understand your physical health status course of illness family history previous medical treatment and examination results We will assign a number to each participant establish a medical record and then perform corresponding psychological assessments magnetic resonance imaging examinations and repeat transcranial magnetic stimulation therapy for two weeks a total of 10 times
Possible Benefits All clinical scale evaluations imaging examinations and repeated transcranial magnetic stimulation interventions related to the study are free of charge Your research doctors and evaluators will conduct timely clinical observations of changes in your condition and provide you with systematic research follow-up and evaluation These evaluations will help make reasonable judgments about your disease status and treatment effectiveness and thus guide treatment decisions more scientifically In addition free treatment with repeated transcranial magnetic stimulation is also beneficial for the improvement of your condition The research team will coordinate with relevant staff in the hospital and department where you are seeking medical treatment to provide convenience in basic clinical services such as doctor appointments registration and waiting in order to save your visit time
Privacy and Confidentiality Issues If you decide to participate in this study your participation in the experiment and your personal information during the experiment will be kept confidential Responsible research doctors and other researchers will use your medical information for research but will not disclose your personal information If you are harmed by participating in this study you can receive free treatment andor corresponding compensation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None