Adolescents' Non-suicidal Behavior and Perception of Parents' Negative Emotional Expression and Family Communication

NCT ID: NCT06290115

Last Updated: 2024-03-13

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 324 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-04-01
• Study Completion Date: 2024-12-31

Brief Summary

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.

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）.

Conditions

Adolescents

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Case group: NSSI patient group

1. Patients who meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI;

2. Age range: 15-25 years old;

3. Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;

Questionnaires set 1

Intervention Type: OTHER

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

1. psychiatric outpatients or inpatients can read and understand the contents of the questionnaire;

2. Patients who do not meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI.

3. Age range: 15-25 years old;

4. Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;

Questionnaires set 2

Intervention Type: OTHER

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

1. No mental illness;

2. Age range: 15-25 years old;

3. Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;

Questionnaires set 3

Intervention Type: OTHER

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.

Interventions

Questionnaires set 1

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）.

Intervention Type: OTHER

Questionnaires set 2

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.

Intervention Type: OTHER

Questionnaires set 3

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.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Patients who meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI;

2. Age range: 15-25 years old;

3. Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;

1. Psychiatric outpatients or inpatients can read and understand the contents of the questionnaire;

2. Patients who do not meet the diagnostic criteria in DSM-5 and are clinically diagnosed as NSSI.

3. Age range: 15-25 years old;

4. Patients and/or guardians can give informed consent and participate in this study.

1. No mental illness;

2. Age range: 15-25 years old;

3. Clear consciousness, normal speech function, able to communicate in Chinese and reading chinese;

4. Patients and/or guardians can give informed consent and participate in this study.

Exclusion Criteria

1. Users with organic diseases and psychoactive substances;

2. NSSI； caused by autism, TIC disorder, mental retardation and other emotional instability and bad mood;

3. Religious self-injury or customary self-injury;

4. 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

1. Patients whose illness causes them unable to communicate or fill out questionnaires;

2. Non-serious mental diseases, such as schizophrenia and schizoaffective disorder.

3.Control group 2: Healthy group

(1) Young people and adolescents who are unable to communicate or fill out questionnaires due to various organic reasons.

• Minimum Eligible Age: 15 Years
• Maximum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Sun Yat-sen University

OTHER

Sponsor Role: lead

Responsible Party

Wei XIA, PhD

associate professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Wei Xia, PhD

Role: PRINCIPAL_INVESTIGATOR

Sun Yat-sen University

Central Contacts

wei Xia, PhD

Role: CONTACT

xiaw23@mail.sysu.edu.cn

18823359471

Yang Liu, Master

Role: CONTACT

nancy_a@126.com

13602299935

Other Identifiers

202301

Identifier Type: -

Identifier Source: org_study_id