Skip to content

Video intervention to improve cognition and attitude of parents of adolescents with non-suicidal self-injury:a randomized controlled clinical study

Construction and effectiveness verification of educational video intervention for non-suicidal self-injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087236
Enrollment
Unknown
Registered
2024-07-23
Start date
2023-06-03
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

non-suicidal self-injury

Interventions

intervention group:Non-suicidal self-injury educational video
control group:A popular science video, unrelated to mental illness or psychiatry, was the same length as the intervention group, and the visual format matched the intervention group video.

Sponsors

The second xiangya hospital of central south university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 53 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for adolescents: (1) Aged between 10-19 years; (2) Meet The non-suicidal self-injury behavioral Diagnostic criteria recommended by The Diagnostic and Statistical Manual of Mental Disorders (DSM-5); (3) Fully understand the research program, voluntarily participate in the research, and sign the informed consent. Inclusion criteria for parents: (1) accompanying adolescents in the psychiatric ward of the second xiangya Hospital; (2) Fully understand the research program, voluntarily participate in the research, and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Parents with severe organic disease could not complete the study; (2) Parents have recently suffered acute stress and are in a stress period (3 months), such as death of relatives, divorce, etc.; (3) Parents with visual impairment, cognitive impairment, neurodevelopmental disorder or other serious mental illness cannot complete the study.

Design outcomes

Primary

MeasureTime frame
non-suicidal self-injury cognitive questionaire;

Secondary

MeasureTime frame
Self-Harm Antipathy Scale;The Affiliate Self-stigma Scale;Family Burden Scale;

Countries

China

Contacts

Public ContactJuan He

Xiangya School of Nursing, Central South University

hejuan@csu.edu.cn+86 185 6960 2460

Outcome results

None listed

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