Salutogenesis Model Care for Adolescent Digital Game Addiction Prevention
Salutogenesis Models
Supportive Care Study
Summary
Study start date: April 1, 2024
Actual date on which the first participant was enrolled.This study aims to address digital game addiction in adolescents, which is increasingly recognized as a significant mental health concern. The research focuses on adolescents due to their high levels of internet and gaming use, which can lead to addiction. This addiction is often exacerbated by stressors common in adolescence, such as family and social pressures, and the anxiety of academic performance. The study employs the Salutogenesis Model, which emphasizes developing a strong sense of integrity to help adolescents manage stress and reduce their reliance on digital games. By strengthening their ability to cope with stress, the study seeks to prevent the onset of digital game addiction, ultimately improving the mental and physical well-being of adolescents. Participants in the study will engage in activities and interventions based on the Salutogenesis Model designed to enhance their internal and external resources. This approach focuses on promoting positive coping strategies and improving their sense of coherence, which includes understanding, managing, and finding meaning in life's demands. Though no specific risks are mentioned, the study intends to provide guidance on improving mental health, vision, physical pain, sleep, nutrition, social contacts, and physical activity. By equipping adolescents with better stress management skills, the study hopes to reduce problematic internet use and prevent digital game addiction, contributing to healthier lifestyles.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care 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 15 to 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location