YouthCOMPASS: The Effectiveness of the Mobile-based Youth COMPASS Program to Promote Adolescent Well-being and Life-control

Sponsor
University of Jyvaskyla (Other)
Overall Status
Completed
CT.gov ID
NCT03274934
Collaborator
the Finnish Cultural Foundation, Central Finland Regional Fund (Other)
249
1
3
27.3
9.1

Study Details

Study Description

Brief Summary

The aim of this randomized control trial is to examine effectiveness of individually tailored web- and mobile-based Acceptance- and Commitment Therapy interventions to promote adolescents' well-being and life-control and subsequently support their successful transition from basic education to upper secondary education. Our additional aim is to examine to what extent the effectiveness of the intervention varies according to intervention intensity and according to risk for school failure. The five-week structured intervention is delivered using the novel web-and mobile-based program Youth COMPASS following the principles of the Acceptance and Commitment Therapy (ACT). The Internet context is assumed to be particularly motivating for youth who enjoy spending time online using different social media. Internet-based interventions have several advantages; they can include more information and treatment components than traditionally delivered treatments and that intervention programs are accessible at any time and at any place. Another unique aspect of the Youth COMPASS is the fact that it is individually-tailored. Each participant have an individually assigned online coach who provides support and encouragement, reminds about Youth COMPASS, sends individualized feedback, and recommends different exercises. The study hypothetizes that the Youth COMPASS is more effective than school counseling as usual. More specifically, the Youth COMPASS is expected to be more effective when it is combined with face-to-face support than when support and feedback are provided only via the Internet. Also, the Youth COMPASS with no face-to-face support (online only) is expected to be more effective than receiving only regular school counseling. Finally, the Youth COMPASS is expected to be more effective for students at risk for school failure than for students without risk for school failure, especially when at risk-adolescents receive more intensive support (i.e., both online and face-to-face support).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Experimental: face-to-face and online support group:
  • Behavioral: Experimental: only online support group:
  • Behavioral: Control
N/A

Detailed Description

The aim of this randomized control trial is to examine effectiveness of individually tailored web- and mobile-based Acceptance- and Commitment Therapy interventions to promote adolescents' well-being and life-control and subsequently support their successful transition from basic education to upper secondary education. Our additional aim is to examine to what extent the effectiveness of the intervention varies according to intervention intensity and according to risk for school failure. The five-week structured intervention is delivered using the novel web-and mobile-based program Youth COMPASS following the principles of the Acceptance and Commitment Therapy (ACT). The Internet context is assumed to be particularly motivating for youth who enjoy spending time online using different social media. Internet-based interventions have several advantages; they can include more information and treatment components than traditionally delivered treatments and that intervention programs are accessible at any time and at any place. Another unique aspect of the Youth COMPASS is the fact that it is individually-tailored. Each participant have an individually assigned online coach who provides support and encouragement, reminds about Youth COMPASS, sends individualized feedback, and recommends different exercises. The study hypothetizes that the Youth COMPASS is more effective than school counseling as usual. More specifically, the Youth COMPASS is expected to be more effective when it is combined with face-to-face support than when support and feedback are provided only via the Internet. Also, the Youth COMPASS with no face-to-face support (online only) is expected to be more effective than receiving only regular school counseling. Finally, the Youth COMPASS is expected to be more effective for students at risk for school failure than for students without risk for school failure, especially when at risk-adolescents receive more intensive support (i.e., both online and face-to-face support). The participants of the effectiveness study of the Youth COMPASS are selected from the participants of the broader longitudinal STAIRWAY (TIKAPUU in Finnish) - From Primary School to Secondary School study, which follows a community sample of Finnish adolescents (n~850) across critical educational transitions. The overall aim of the STAIRWAY project is to broaden our understanding of the individual- and environment-related factors that promote learning, well-being and successful educational transitions.

Study Design

Study Type:
Interventional
Actual Enrollment :
249 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Treatment, Parallel assessment, Randomized, Efficacy studyTreatment, Parallel assessment, Randomized, Efficacy study
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Effectiveness of the Novel Web- and Mobile-based Acceptance- and Commitment Therapy Program Youth COMPASS to Promote Adolescent Well-being and Life-control
Actual Study Start Date :
Sep 21, 2017
Actual Primary Completion Date :
Dec 15, 2017
Actual Study Completion Date :
Dec 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Face-to-face and online support group

Behavioral: Structured web- and mobile-based intervention with Youth COMPASS program to support adolescents' well-being, career preparation and life-control and subsequently support successful transition to upper secondary education. The Youth COMPASS is the five-week online program according to principles of Acceptance and Commitment Therapy aiming to enhance adolescents' psychological flexibility by guiding adolescents in exploring their values and setting goals and changing behaviors according to their goals (week 1), and learning acceptance defusion and mindfulness skills (weeks 2-3) and integrating these skills into their personal life (weeks 4-5). The participants in this condition receive weekly online support and feedback from their individually assigned coach. In addition, they meet their coach twice in the face-to-face meetings. The aim of the meetings is to increase adolescents' internal motivation and thereby participation in the program.

Behavioral: Experimental: face-to-face and online support group:
5-week intervention according to Acceptance and Commitment Therapy principles with the web-and mobile-based Youth COMPASS program, face-to-face support (2 meetings) and weekly online mobile support and feedback from the individually assigned coach (one third of the participants is randomly assigned to this group)

Experimental: Only online support group

Behavioral: web- and mobile-based intervention with Youth COMPASS program to support adolescents' well-being, career preparation and life-control and subsequently support successful transition to upper secondary education. The Youth COMPASS is a five-week online program according to principles of Acceptance and Commitment Therapy aiming to enhance adolescents' psychological flexibility by guiding adolescents in exploring their values and setting goals and changing behaviors according to their goals (week 1), and learning acceptance defusion and mindfulness skills (weeks 2-3) and integrating these skills into their personal life (weeks 4-5). The participants in this condition receive weekly online support and feedback from their individually assigned coach.

Behavioral: Experimental: only online support group:
5-week intervention according to ACT principles with the web-and mobile-based Youth COMPASS program, no face-to-face support, weekly mobile online support and feedback from the individually assigned coach (one third of the participants is randomly assigned to this group)

Experimental: Control group

Behavioral: No intervention, school counseling as usual

Behavioral: Control
Control group, no intervention, school counseling as usual. (one third of the participants is randomly assigned to this group)

Outcome Measures

Primary Outcome Measures

  1. Life satisfaction (Diener et al., 1985) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  2. Self-esteem (Rosenberg, 1965), [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  3. Depressive symptoms (Salokangas et al., 1995) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  4. Stress (Elo et al., 2003) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  5. Difficulties and Strenghts questionnaire (SDQ, Goodman et al. 1997) measuring emotional symptoms, hyperactivity, conduct problems and prosociality [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  6. Well-being in school (World Health Organization) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  7. Career choice preparedness (Koivisto et al., 2011) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  8. Educational expectations [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

Secondary Outcome Measures

  1. Psychological flexibility (Greco et al., 2008) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  2. Mindfulness skills (Ciarrochi et al., 2011) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  3. Identity formation (DIDS; Luyckx et al., 2008; see also Marttinen et al., 2016) [Change from baseline at 2, 6, 12 and 18 months after the intervention]

    In addition to self-reports, also school register information is collected regarding academic performance, school absences and progress in studies.

  4. Truancy [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  5. School grades [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

  6. Initiation of upper secondary education [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

  7. Progress in upper secondary studies [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

  8. Changes in study field in upper secondary education [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

  9. Staying in vs. dropping out of education [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

  10. Graduation time [Four years from the baseline.]

    In addition to self-reports, also school register information is collected.

Other Outcome Measures

  1. Achievement strategies (Nurmi et al., 1995) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  2. Academic buoyancy (Martin & Marsh, 2008) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  3. Recovery from school work (see also Winwood et al., 2005) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  4. Child-Parent relationship (Pianta, 1992) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  5. Student-Teacher relationship (Pianta, 2001) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  6. Best Friend-Student (Bukowski et al., 1994) relationship [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  7. Temperament (Rothbart & Ellis, 2001) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  8. Substance use (Rimpelä et al., 2003) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  9. Loneliness (World Health Organization) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  10. Health behaviors (World Health Organization) [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  11. Dating [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

  12. Having hobbies [Change from baseline at 2, 6, 12 and 18 months after the intervention.]

    Study has five timepoints when same questionnaires are administered to assess possible changes in the outcome measures.

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adolescents (n = 120) who have risk for school failure (learning difficulties or low grade point average without learning difficulties)

  • Randomly chosen adolescents (n=120) from the same classrooms who have no risk for school failure

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Psychology, University of Jyväskylä Jyväskylä Finland 40014

Sponsors and Collaborators

  • University of Jyvaskyla
  • the Finnish Cultural Foundation, Central Finland Regional Fund

Investigators

  • Principal Investigator: Noona Kiuru, PhD, Department of Psychology, University of Jyväskylä, Finland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Jyvaskyla
ClinicalTrials.gov Identifier:
NCT03274934
Other Study ID Numbers:
  • 21000039071
First Posted:
Sep 7, 2017
Last Update Posted:
Apr 2, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Jyvaskyla

Study Results

No Results Posted as of Apr 2, 2020