- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06290115
Adolescents' Non-suicidal Behavior and Perception of Parents' Negative Emotional Expression and Family Communication
March 12, 2024 updated by: Wei XIA, PhD, Sun Yat-sen University
Relationship Between Non-suicidal Self-injury Behaviors in Adolescents and Young Adults and Perceived Parental Negative Emotional Expression and Family Communication Styles in Children:A Case-control Study
The starting point of this project is to study young people and adolescents, aiming to explore the correlation between non-suicidal behavior of young people and adolescents and the negative emotional expression of their parents and family communication.
The purpose of this project is to investigate the non-suicidal self-injury behavior of teenagers aged 15-25 years by issuing questionnaires (sample size: 327 people).
In order to find out whether there is any connection between family communication and non-suicidal self-injury behavior of young people and adolescents.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The incidence of non-suicidal self-injury(NSSI) among adolescents has obviously increased, which should attract the attention of the whole society.
Their mental health problems will not only lead to personal pain and family burden, but also bring potential negative effects to future social development.
Therefore, it is necessary to study the psychological problems of teenagers and their influencing factors.
This study will conduct a case-control study from the perspective of family, and analyze the negative emotional expression and family communication style of parents of non-suicidal teenagers and their influence on non-suicidal self-injury behavior.
This study is conducted in the form of scale, which will use the demographic information,the Family Emotional Expressivity Questionnaire(FEEQ)、the Parent-Adolescent Communication Scale(PACS)、the Childhood Trauma Questionnaire(CTQ)、the Parental Bongding Instrument(PBI)、the Adolescent parent-child relationship intimacy questionnaire and the Ottawa Self-injury Inventory(OSI).
Study Type
Observational
Enrollment (Estimated)
324
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: wei Xia, PhD
- Phone Number: 18823359471
- Email: xiaw23@mail.sysu.edu.cn
Study Contact Backup
- Name: Yang Liu, Master
- Phone Number: 13602299935
- Email: nancy_a@126.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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The group of adolescents and young adults diagnosed as NSSI, and the control group includes adolescents and young adults with other mental diseases other than NSSI, healthy adolescents and young adults.
Description
1.Case group: NSSI patient group:
Inclusion Criteria:
- Patients who meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI;
- Age range: 15-25 years old;
- Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;
Exclusion Criteria:
- Users with organic diseases and psychoactive substances;
- NSSI; caused by autism, TIC disorder, mental retardation and other emotional instability and bad mood;
- Religious self-injury or customary self-injury;
- Patients with schizophrenia, schizoaffective disorder, alcohol dependence, organic mental disorder and other mental disorders have been previously diagnosed.
2.Control group 1: Non-NSSI patients
Inclusion criteria:
- Psychiatric outpatients or inpatients can read and understand the contents of the questionnaire;
- Patients who do not meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI.
- Age range: 15-25 years old;
- Patients and/or guardians can give informed consent and participate in this study.
Exclusion criteria:
- Patients whose illness causes them unable to communicate or fill out questionnaires;
- Non-serious mental diseases, such as schizophrenia and schizoaffective disorder.
3.Control group 2: Healthy group
Inclusion criteria
- No mental illness;
- Age range: 15-25 years old;
- Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;
- Patients and/or guardians can give informed consent and participate in this study.
Exclusion criteria
(1) Young people and adolescents who are unable to communicate or fill out questionnaires due to various organic reasons.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Case group: NSSI patient group
|
Participants of case group will be asked to respond to the demographic information,the Family Emotional Expressivity Questionnaire(FEEQ)、the Parent-Adolescent Communication Scale(PACS)、the Childhood Trauma Questionnaire(CTQ)、the Parental Bongding Instrument(PBI)、the Adolescent parent-child relationship intimacy questionnaire and the Ottawa Self-injury Inventory(OSI).
|
|
Control group 1: non-NSSI patients
|
Participants of control group 1 will be asked to respond to the demographic information,the Family Emotional Expressivity Questionnaire(FEEQ)、the Parent-Adolescent Communication Scale(PACS)、the Childhood Trauma Questionnaire(CTQ)、the Parental Bongding Instrument(PBI) and the Adolescent parent-child relationship intimacy questionnaire.
|
|
Control group 2: healthy group
|
Participants of control group 2 will be asked to respond to the demographic information,the Family Emotional Expressivity Questionnaire(FEEQ)、the Parent-Adolescent Communication Scale(PACS)、the Childhood Trauma Questionnaire(CTQ)、the Parental Bongding Instrument(PBI) and the Adolescent parent-child relationship intimacy questionnaire.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Non-suicidal self-injury behavior of young people and adolescents
Time Frame: Baseline
|
There are 28 items in the Ottawa Self-injury Inventory, which are used to evaluate the frequency of NSSI and suicide in the last 1, 6 and 12 months, the age of first onset, the source and concealment of self-injury ideas, and the feeling of self-injury impulse.
|
Baseline
|
|
Expression of negative emotions of parents
Time Frame: Baseline
|
There are 40 items in the Parental Emotional Expression Questionnaire, which is used to measure parents' negative emotions.
The scale adopts system, and the higher the dimension score, the greater the possibility of negative emotions.
|
Baseline
|
|
Parent-Adolescent communication scale
Time Frame: Baseline
|
There are 40 items in the parent-Adolescent communication scale, which is used to measure parent-child communication.
The scale adopts Likert 5-point system, and the higher the score, the better the parent-child communication.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Childhood Trauma Questionnaire
Time Frame: Baseline
|
There are 28 items in the Childhood Trauma Scale, which are used to measure childhood traumatic experiences.
The scale adopts Likert 5-point system, and the higher the score, the more serious the childhood trauma experience.
|
Baseline
|
|
Parental Bongding Instrument
Time Frame: Baseline
|
There are 23 items in the Parenting Style Scale, which is used to measure the parenting style.
The scale adopts Likert 4-point system, which consists of three factors: caring, encouraging autonomy and controlling.
|
Baseline
|
|
The parent-child relationship intimacy scale
Time Frame: Baseline
|
There are 29 items in the parent-child relationship intimacy scale, which are used to measure the parent-child relationship.
The scale adopts Likert 5-point system, and the higher the score, the higher the intimacy of parent-child relationship.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Wei Xia, PhD, Sun Yat-sen University
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 (Estimated)
April 1, 2024
Primary Completion (Estimated)
October 31, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
February 26, 2024
First Submitted That Met QC Criteria
February 26, 2024
First Posted (Actual)
March 4, 2024
Study Record Updates
Last Update Posted (Actual)
March 13, 2024
Last Update Submitted That Met QC Criteria
March 12, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202301
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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