- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01314521
Suicidal Ideation and Behavior in Korean Adolescents With Depression
October 4, 2011 updated by: Hallym University Medical Center
The purpose of this study is to examine clinical characteristics of Korean adolescents with depression who have suicidal ideation and behavior. We formulate those hypotheses.
- Being bullied in peer relationships, excessive use of internet, excessive extra-curricular tutoring, sexual abuse in childhood, physical abuse and emotional neglect are risk factors of suicide in adolescents.
- Depression of parents and negative child-rearing attitude are risk factors of suicidal ideation and behavior in adolescents.
- Emotional quotient (EQ) and resilience of adolescent are protective factors of suicide.
Study Overview
Status
Unknown
Conditions
Detailed Description
Korea has reported the highest suicide rate among OECD members and according to the data from the Korea national statistical office, suicide is the second major cause of death in adolescents and is increasing.
Depression, one of the well-known risk factors of suicide in adolescents, can cause maladjustments to school and family life, problems of interpersonal relationship and drug abuse so that work to trigger the suicidal ideation and behavior.
In his study, we planned to examine the relationship between suicidal ideation and behavior and several risk factors by using the standardized diagnostic clinical interview, especially an objective suicide evaluating method which has recently developed.
Study Type
Observational
Enrollment (Anticipated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mina Song, MD
- Phone Number: +82-10-4760-2990
- Email: blue-oboe@hanmail.net
Study Contact Backup
- Name: Hyun Ju Hong, MD, PhD
- Phone Number: +82-31-380-3751
- Email: honghj88@gmail.com
Study Locations
-
-
Kyeonggi Do
-
Anyang Si, Kyeonggi Do, Korea, Republic of, 431-070
- Recruiting
- Hallym University Sacred Heart Hospital
-
Contact:
- Mina Song, MD
- Phone Number: +82-10-4760-2990
- Email: blue-oboe@hanmail.net
-
Contact:
- Hyun Ju Hong, MD, PhD
- Phone Number: +82-31-380-3751
- Email: honghj88@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
outpatients of university hospitals.
50 from Hallym University Sacred Heart Hospital, 50 from Bundang CHA Hospital, 50 from Myongji Hospital.
Description
Inclusion Criteria:
- a subject who has depression (Major depressive disorder, dysthymic disorder, depressive disorder NOS) diagnosed by Kiddie-Schedule for affective disorder and schizophrenia (K-SADS-PL-K)
- subjects and their family (a parent or a grandparent) or their legal representative consent to participate in this study voluntarily
- subjects and their family (a parent or a grandparent) or their legal representative are able to understand the meaning of participation in this study and able to reject or ask to leave from this study
Exclusion Criteria:
- a patient who has diagnosed with bipolar disorder, psychotic disorder, pervasive developmental disorder, organic brain disease, or epilepsy
- a patient with mental retardation who is IQ under 70
- a patient who has a severe medical illness (chronic physical disease, cardiovascular, hepatobiliary, nephrology, or respiratory disease and so on)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Columbia Suicide Severity Rating Scale; C-SSRS
Time Frame: baseline only (at any one point during the depressive episode)
|
Semi-structured clinical interview based on the systematic guideline which help draw inferences about suicidal ideation from clinical situation and risk factors related to the suicide.
It is composed with three categories that are suicidal attempt (ideation), non-suicidal attempt (ideation), and potential of suicidal attempt (ideation).
|
baseline only (at any one point during the depressive episode)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Beck suicidal ideation scale
Time Frame: baseline only
|
self report form of 19 items with 3 point scale.
for subjects and their parents.
|
baseline only
|
Revised Children's Manifest Anxiety Scale; RCMAS
Time Frame: baseline only
|
baseline only
|
|
Beck Depression Inventory
Time Frame: baseline only
|
baseline only
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hyun Ju Hong, MD, PhD, Hallym University Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2011
Study Completion (ANTICIPATED)
March 1, 2012
Study Registration Dates
First Submitted
March 9, 2011
First Submitted That Met QC Criteria
March 11, 2011
First Posted (ESTIMATE)
March 14, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
October 5, 2011
Last Update Submitted That Met QC Criteria
October 4, 2011
Last Verified
March 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SKAD
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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