Digital Mental Health Intervention for Adolescents with Nonsuicidal Self-injury
This study aims to evaluate the acceptability and appropriateness of a digital mental health intervention for adolescents who engage in nonsuicidal self-injury.
App-based digital mental health intervention for adolescent NSSI
+ App-based delivery of healthy living psychoeducational materials
Anxiety Disorders+3
+ Behavior
+ Mental Disorders
Treatment Study
Summary
Study start date: January 1, 2026
Actual date on which the first participant was enrolled.This study focuses on creating and testing a new digital mental health tool for teenagers aged 14 to 18 who engage in nonsuicidal self-injury (NSSI). It targets adolescents not currently in treatment and aims to provide them with psychoeducation and skills through an interactive digital platform. This tool is important because it could offer a new way to support young people struggling with self-injury, helping them learn new skills and potentially reducing the frequency and severity of their self-injury behaviors. The study addresses a significant need for accessible mental health resources for adolescents who might not seek traditional forms of treatment. Participants in the study are randomly assigned to one of two groups: one group receives the digital mental health intervention, while the other receives a psychoeducational control over eight weeks. The digital intervention includes engaging activities and interactive conversations aimed at teaching coping skills. Researchers will measure the success of this study by looking at how often and how severely participants engage in self-injury, as well as their willingness to seek help. The study also evaluates how acceptable and appropriate participants find the intervention. Participants must have access to a smartphone, be proficient in English, and cannot have severe mental health conditions or be at high risk of suicide. They are allowed to seek other treatments once they join the study.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 14 to 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives