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Opp - a Universal Mental Health Promoting Mobile Application for Adolescents

U

University of Tromso (UiT)

Status

Active, not recruiting

Conditions

Mental Health Wellness 1

Treatments

Device: Opp

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of the project is firstly, to develop an app-based mental health intervention for adolescents. Secondly, to evaluate the effect of this app. The overarching goal is to offer a low-threshold intervention, called Opp, that is easily accessible and free to use for all adolescents in Norway.

Full description

The intervention "Opp" will be delivered through a mobile application. The overall goals of Opp are to 1) increase well-being and mental well-being, 2) increase knowledge about mental health, 3) increase coping skills to deal with stress, 4) increase help-seeking behavior, 5) increase self-esteem, 6) increase sleep quality and 7) reduce mental health problems.

To evaluate the mobile application two studies will be conducted: A user survey and an effectiveness study with a follow-up examination after about six weeks. The effectiveness study will be conducted as a randomized controlled trial with an intervention group and a waiting-list control group.

Enrollment

700 estimated patients

Sex

All

Ages

13 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adolescents under 16 years whose guardians have given consent

Exclusion criteria

  • severe developmental or cognitive challenges

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

700 participants in 2 patient groups

Intervention group receiving Opp
Experimental group
Description:
The effectiveness study will be conducted as a randomized controlled trial with an intervention group and a waiting-list control group. Data will be collected at baseline (T1, pre intervention) and after about six weeks of intervention (T2, post intervention).
Treatment:
Device: Opp
Control group
No Intervention group
Description:
The waiting list control group will receive the intervention after study completion.

Trial contacts and locations

1

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Central trial contact

Henriette Kyrrestad, PhD; Sabine Kaiser, PhD

Data sourced from clinicaltrials.gov

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