Accepted for/Published in: JMIR Research Protocols
Date Submitted: Nov 18, 2024
Date Accepted: Oct 1, 2025
Improving digital mental health services with and for national minority, Indigenous and refugee youth in Norway: The InvolveMENT multi-phase mixed methods research project protocol
ABSTRACT
Background:
Worldwide, minority youth less commonly receive culturally sensitive mental health services than the majority peer population. In Norway, limited research exists on the mental health and service use among youth from national minority (Forrest Finns, Kven/Norwegian Finns, Jews, Roma, and Romani), Indigenous (Sámi), and refugee backgrounds. Although the Norwegian government provides a public communication channel for youth, including mental health information and support, digital services have not been adapted to meet the needs of these groups. There is no research to determine the use, acceptability, effectiveness, cost-effectiveness and safety of these services for these youth.
Objective:
: The main aim of the InvolveMENT project is to improve the mental health of national minority, Indigenous and refugee youth. The project’s objectives are, for these groups of youth, to: (1) Determine mental health and digital support needs, and possible barriers and facilitators to service use; (2) Assess use of and satisfaction with digital services to meet their mental health needs; (3) Explore their perspectives on digital mental health services; (4) Develop recommendations which can be used to adapt digital services to meet their needs and rights; and (5) Assess the use, acceptability, satisfaction, effectiveness, cost-effectiveness and safety of adapted services.
Methods:
The four-year InvolveMENT project consists of four phases: 1) Establishing a longitudinal cohort consisting of national minority, Indigenous and refugee youth, using surveys to assess their mental health, wellbeing, digital support needs, utilization and satisfaction with digital services, and possible barriers and facilitators to service use. 2) Conducting qualitative interviews with minority youth to explore their perspectives, and synthesizing data from phase 1 and 2 for a mixed methods analysis. 3) Involving youth, and healthcare and other professionals to develop proposals to adapt and improve the existing digital services. 4) A randomised controlled trial (RCT) and a qualitative study to evaluate the adapted services.
Results:
Cohort and qualitative study designs are completed. Ethics applications have been approved, and recruitment to the cohort and qualitative studies have started.
Conclusions:
The InvolveMENT project has the potential to enhance the accessibility and quality of healthcare services, early interventions, reduce inequality in service provision for minority groups, and strengthen collaboration between youth, public and research organizations. Through this, it has the potential to improve mental health of youth from these groups. Findings might be transferable to other minority groups, both nationally and internationally. Clinical Trial: ISRCTN21223142 https://doi.org/10.1186/ISRCTN21223142
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