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Youth Compass Plus

Not Applicable
Completed
Conditions
Psychological Flexibility
Psychological Well-being
Interventions
Behavioral: Control group, no intervention
Behavioral: face-to-face support and Chatbot online support group
Behavioral: only chat-robot online support group
Registration Number
NCT04340206
Lead Sponsor
University of Jyvaskyla
Brief Summary

The aim of this randomized control trial is to examine the effectiveness of a novel web- and mobile-based Acceptance and Commitment Therapy program (Youth Compass plus) to promote adolescents' psychological flexibility and well-being and subsequently support their successful transition from basic education to upper secondary education. Our aim is also to compare the efficacy of Youth Compass plus using either an eCoach providing automated personal support to the user or an eCoach and a Human Coach providing personal support to the user. Additionally, we will investigate whether the efficacy of the Youth Compass plus varies according to different individual and contextual factors.

Using the internet to deliver interventions is assumed to be particularly motivating for youth who enjoy spending time online using different social media. Web-based interventions have several advantages; they can include more information and treatment components than traditionally delivered treatments and they are accessible at any time and place. The five-week structured intervention is delivered using the novel web- and mobile-based program Youth Compass plus. Youth Compass plus has been developed based on the feedback for the Youth COMPASS pilot program (see ClinicalTrials.gov, NCT03274934). The exercises of Youth Compass plus have been modified, visual aspects have been improved and new game-based interactive elements have been developed. In the Youth COMPASS pilot study, psychology students acted as (human) coaches for the users. While interaction with a personal coach increases commitment to the program, the need to train and supervise coaches limits large scale dissemination. To provide an alternative that is less demanding in terms of resources, we have developed a chatbot (eCoach) as a new feature within the new Youth Compass plus program. The automated eCoach provides personal support within the program and via text messages. The eCoach provides support and encouragement, reminds about using Youth Compass plus, sends individualized feedback, and recommends different exercises.

Detailed Description

The aim of this randomized trial is to examine whether Youth Compass plus enhances adolescents' (a) psychological skills, particularly with respect to finding a purpose, and psychological flexibility and adaptation skills as the ACT process outcomes; (b) career preparation and psychological well-being as the proximal outcomes; and (c) the initiation of upper secondary education studies and engagement in upper secondary education as the distal outcomes.

In addition, our aim is to investigate the ACT processes and mediating mechanisms of the Youth Compass plus program, and to explore the extent to which the effectiveness of the Youth Compass plus varies according to the differences in various individual and contextual factors.

H1: The study expects that the Youth Compass plus is more effective than no intervention. Youth Compass plus is expected to promote ACT proximal youth outcomes, as well as the youth distal outcomes.

H2: In addition, the study expects that the Youth Compass plus will promote the distal outcomes through enhancing the ACT process outcomes and the proximal outcomes.

H3: The study expects that Youth Compass plus is more effective for those adolescents who accept the intervention well, take part intensively and diversely in different exercises, as well as among the adolescents who are initially highly emotionally reactive.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
348
Inclusion Criteria

Not provided

Exclusion Criteria

Approximately 600-1000 Finnish 14-16 year old adolescents from non-clinical school-age population will fill in a pre-questionnaire. Based on this data the participants for the randomized control trial will be selected from the two gender-balanced groups of Finnish adolescents:

  1. Adolescents (n = 150) who have heightened (pre-clinical) level of symptoms of stress/anxiety/depression in the screening measures (no diagnosis is required for participation).
  2. Randomly chosen adolescents (n=150) who have no symptoms of stress/anxiety/depression in the screening measures

Adolescents from both groups are randomly assigned in three conditions: (a) five weeks of Youth Compass plus with support from chatbot + face-to-face support (altogether two face-to-face meetings); b) five-weeks of Youth Compass plus with support from chatbot only; or (c) no intervention. At the baseline (fall 2020) the participants will be ninth-graders facing the transition to upper secondary education.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental ControlControl group, no interventionExperimental Control: Control group, no intervention (one third of the participants is randomly assigned to this group)
face-to-face support and Chatbot online support groupface-to-face support and Chatbot online support groupExperimental, Intervention Group A: face-to-face support and Chatbot online support group: 5-week intervention according to ACT principles with the web- and mobile-based Youth Compass plus program, face-to-face support (2 meetings) and weekly online support and feedback from the Chabot eCoach built within the program (one third of the participants is randomly assigned to this group)
only chat-robot online support grouponly chat-robot online support groupExperimental, Intervention Group B: only chat-robot online support group: 5-week intervention according to ACT principles with the web-and mobile-based Youth Compass plus program, no face-to-face support, and weekly online support and feedback from the chatbot eCoach built within the program (one third of the participants is randomly assigned to this group)
Primary Outcome Measures
NameTimeMethod
psychological flexibilityChange from baseline at 2 and 6 months after the intervention

Cognitive Fusion Questionnaire (Gillanders et al., 2014)

life satisfactionChange from baseline at 2 and 6 months after the intervention

Satisfaction with Life Scale, SWLS, Diener et al., 1985

mental well-beingChange from baseline at 2 and 6 months after the intervention

Warwick-Edinburgh Mental Well-being Scale WEMWBS; THL 2011

stress symptomsChange from baseline at 2 and 6 months after the intervention

Perceived Stress Scale, PSS-10; Cohen et al., 1983

anxiety symptomsChange from baseline at 2 and 6 months after the intervention

short-form of the state scale of the Spielberger State-Trait Anxiety Inventory, STAI; Marteau \& Becker, 1992

depressive symptomsChange from baseline at 2 and 6 months after the intervention

Depression Scale, DEPS; Salokangas et al., 1995

Career choice preparednessChange from baseline at 2 and 6 months after the intervention

career choice self-efficacy, career-related insecurity, preparation against setbacks, Koivisto et al., 2011

Secondary Outcome Measures
NameTimeMethod
perfectionismChange from baseline at 2 and 6 months after the intervention

The Child-Adolescent; Perfectionism Scale, CAPS; Gordon et al., 2016

self-compassionChange from baseline at 2 and 6 months after the intervention

Self-Compassion Scale - Short Form; Raes et al., 2011

prosocial aspirationsChange from baseline at 2 and 6 months after the intervention

short form of the Aspirations Index, Marshall, 2019

academic buoyancyChange from baseline at 2 and 6 months after the intervention

short Academic buoyancy scale; Martin \& Marsh, 2008

school well-beingChange from baseline at 2 and 6 months after the intervention

school satisfaction, anti-school attitude, school-related stress, WHO

academic performanceChange from baseline at 2 and 6 months after the intervention

grade point average

truancy and school absencesChange from baseline at 2 and 6 months after the intervention

truancy and school absences, Finnish School Health Questionnaire

educational attainment, information from school registers2020-2025 (not possible to provide more specitic time frame)

initiation of upper secondary education, progress in studies, changes in study field, graduation time,

Trial Locations

Locations (1)

Department of Psychology University of Jyvaskyla

🇫🇮

Jyvaskyla, Finland

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