Discovering Adolescents' Talents and Life Projects as a Key Factor in Their Life Satisfaction (GENIALADOLES)

November 15, 2024 updated by: María Beltrán-Ortega, Centre Besai

Recent data show a deterioration in the mental health of adolescents, with an increase in anxiety, depression, sleep disturbances, eating disorders, and a significant increase in suicides. Psychological distress may be related to the absence of a life project that provides motivation, satisfaction, and direction in their lives, and allows the formation of an integrated sense of personal identity, along with a projection of improvement in abilities. An intervention aimed at enhancing the life project of adolescents could increase their life satisfaction and, secondarily, improve their mental health. The goal of this clinical trial is to learn if a structured intervention oriented towards the discovery and development of personal talents can have a strong positive impact on the life satisfaction and mental health of adolescents.

The Spanish versions of the Satisfaction with Life Scale and Young Person-Clinical Outcomes in Routine Evaluation scales will be used to evaluate life satisfaction and psychological distress of participants before and after the intervention. In addition, the Geniotype questionnaire will be used to explore and enhance the participants' personal talents.

The full intervention comprises eight sessions based on Humanistic Integrative Psychotherapy (HIP). It includes one session with Explore Your Meanings (EYME), an immersive digital platform based on the repertory grid technique aimed to enhance the success of therapeutic work and improve personal capabilities.

Researchers will compare the full intervention, with an intervention in which the Geniotype questionnaire is substituted by a somatic symptoms questionnaire (with no implications for the talents of the participant) to see if the Geniotype identification works to increase life satisfaction and reduce psychological distress. The control group will be a non-active waiting list.

Participants will attend eight weekly, one-hour sessions of a psychological intervention including Geniotype or a somatic symptoms questionnaire or remain in a waiting list for 2 months.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This study addresses the growing concern over adolescent mental health deterioration. There is an increase in psychiatric disorders like anxiety, depression, sleep, and eating disorders, as well as suicide attempts. Added to life stage stress is the anguish from a lack of existential meaning, possibly due to the absence of a life project providing motivation and direction. Humanistic and existential psychology views a life project as central to development, promoting well-being and self-realization.

Identity processes are essential for adolescents. Personal Construct Theory focuses on personal identity, understood as the core constructs of a wider system with which people understand and predict events, and generate personal goals. Using the Explore Your Meanings (EYME) tool, a virtual reality (VR) technology platform based on the repertory grid technique, the goal is to observe the evolution of constructing a life project closer to the ideal self. This intervention allows participants to explore their identity within their personal world of meanings in a safe environment.

The concept of Geniotype, created by Tony Estruch in 2022, highlights individual talents and strengths, classifying skills and abilities for vocational guidance. This information helps frame an adolescent's professional life project, preventing school failure, low self-esteem, and mental health issues. The Geniotype test offers valuable insights for adolescents at a crucial stage where society demands clarity about their professional future.

The investigators start from the idea that an intervention focused on adolescents' life projects could enhance their life satisfaction and, secondarily, their mental health. To achieve these goals, they developed a therapeutic protocol based on Humanistic Integrative Psychotherapy (HIP). This model uses a broad range of integrative techniques to help construct and develop life projects, considering the therapeutic relationship and individual peculiarities. The model has shown favorable results in adults with depression and personality disorders, and in benzodiazepine deprescription.

The main objective of this research is to improve adolescents' life satisfaction using a protocol based on EYME and HIP, incorporating the concept of Geniotype. Additionally, the relationships between variables evaluated at the start, including sociodemographic factors with a focus on gender and age, will be explored.

PROCEDURE Recruitment and Enrollment: Public and private schools in Catalonia will be contacted to inform families about the research via email and Centre Besai's Instagram profile. Information and participation forms will be available on Centre Besai's website. Volunteers will apply through the website, undergo a welcome interview, and, if eligible, will be randomly assigned to one of three groups.

Assessment and Intervention: Psychologists trained in HIP, EYME, and Geniotype work will conduct assessments and interventions. Participants will provide sociodemographic data and complete the Spanish versions of the Satisfaction with Life Scale and Young Person-Clinical Outcomes in Routine Evaluation scales, initially and after 8 weeks. Experimental groups will receive eight one-hour sessions based on the protocol, while the control group will remain in the waiting list. After the second evaluation, the control group may join a group intervention.

EXPECTED IMPACT ON PARTICIPANTS

No harmful effects have been identified in the psychological treatments used in the study. However, precautions will be taken to prevent potential side effects from VR intervention. VR may cause mild discomfort like dizziness or nausea. To minimize risks:

Virtual environments will be stable, reacting only to user actions. Techniques like teleportation will minimize movement and side effects. Participants will promptly report any side effects to the therapist, who will halt the session until discomfort subsides.

After each session, participants will remain seated briefly to ensure any discomfort dissipates. If discomfort persists, they will stay seated with the therapist until fully recovered.

DATA ANALYSIS Descriptive analyses will include means, standard deviations, medians, interquartile ranges, frequencies, and percentages, assessing distribution normality using relevant tests. From repertory grid data, cognitive indices like current self-ideal self discrepancy, cognitive differentiation, polarization, presence of dilemmatic constructs, and implicative dilemmas will be obtained using GRIDCOR 6.0 software.

Intervention efficacy will be assessed via repeated measures analysis of variance on pre and post questionnaire scores, with Levene's test for variance heterogeneity and Bonferroni correction for multiple comparisons. Analyses will be adjusted for covariates such as age, gender, and sociodemographic conditions, with confidence intervals and effect sizes calculated. It is expected that the analyses will show a significant improvement in life satisfaction and a reduction in psychological distress in adolescents participating in the experimental groups compared to the control group Exploratory analyses will examine gender and migratory status differences, and correlations between baseline variables will be calculated.

DATA MANAGEMENT PLAN The data management will adhere to these principles: Findable, Accessible, Interoperable, and Reusable (FAIR). Data will be collected automatically at baseline, post-intervention, and follow-up, stored securely on Centre Besai's cloud platform. Researchers will maintain strict confidentiality regarding participants' personal information and pledge not to misuse or disclose it. Personal data will be securely stored in locked cabinets and encrypted hard disks, with access restricted to the principal investigator. Data analysis will use pseudo-anonymized databases to protect participant identities. All participants will adhere to relevant data protection laws, ensuring compliance with Organic Law 15/1999, Royal Decree 1720/2007, and Regulation 2016/679.

Study Type

Interventional

Enrollment (Estimated)

90

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Spain
    • Catalonia
      • Barcelona, Catalonia, Spain, 08007
        • Recruiting
        • Centre Besai
        • Contact:
        • Sub-Investigator:
          • Guillem Feixas, PhD
        • Sub-Investigator:
          • Paloma Vicens, PhD
        • Sub-Investigator:
          • Mikel Marquiegui, BS Psych

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Be a teenager between the ages of 14 and 18 (both included) and be in school.

Exclusion Criteria:

  • Diagnosis of mental disorder in the last year.
  • Active psychological or psychiatric treatment at the time of the investigation or less than 6 months before.
  • Suicidal ideation and/or self-harm.
  • Recently experienced bullying or intimidation (within the last 6 months).
  • Habitual consumption of drugs of abuse (chemical substances of various origins consumed for non-therapeutic purposes).
  • Insufficient level of proficiency in Spanish or Catalan.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Wait List Control (WLC)
Wait List Control
Experimental: Humanistic Integrative Psychotherapy and Identity Exploration (HIP+EYME)
Humanistic Integrative Psychotherapy and Identity Exploration with Virtual Reality using Explore Your Meanings (EYME)
Behavioral: Experimental: Humanistic Integrative Psychotherapy and Identity Exploration (HIP+EYME)
Eight weekly, one-hour sessions based on HIP (including techniques such as analyzing transactions, recognizing ego states, script analysis, letter to my future self --10 years from now, psychoeducation on emotional intelligence, chair work with subpersonalities, fearful scene work, imaginal work with the life project) and the immersive exploration of personal identity using EYME.
Experimental: Humanistic Integrative Psychotherapy, Identity, and Geniotype Exploration (HIP+EYME+GENIOTYPE)
Humanistic Integrative Psychotherapy, Identity Exploration with Virtual Reality using Explore Your Meanings, and Geniotype characterization
Behavioral: Experimental: Humanistic Integrative Psychotherapy, Identity, and Geniotype Exploration (HIP+EYME+GENIOTYPE)
Eight weekly, one-hour sessions based on HIP (including techniques such as analyzing transactions, recognizing ego states, script analysis, letter to my future self --10 years from now, psychoeducation on emotional intelligence, chair work with subpersonalities, fearful scene work, imaginal work with the life project) and the immersive exploration of personal identity using EYME. Also, participants will answer the Geniotype questionnaire and the results will be worked with the adolescents.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction with Life Scale (SWLS)
Time Frame: SWLS will be administered at baseline, and at the end of the last (8th.) session (2 months).
The SWLS is an instrument used in research on quality of life and psychological well-being. It is a brief 5-item instrument using a 7-point Likert scale designed to measure individuals' global cognitive judgments of satisfaction with their life. The higher the score, the higher the level of satisfaction.
SWLS will be administered at baseline, and at the end of the last (8th.) session (2 months).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Young Person-Clinical Outcomes in Routine Evaluation (YP-CORE)
Time Frame: YP-CORE will be administered at baseline, and at the end of the last (8th.) session (2 months).
Designed for adolescents aged 11-16, the YP-CORE assesses wellbeing, problems/symptoms, general functioning, and risk with 10 items using a 5-point Likert scale (0-4). The higher the score, the higher the level of psychological distress. The Spanish adaptation demonstrates good psychometric properties.
YP-CORE will be administered at baseline, and at the end of the last (8th.) session (2 months).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centre Besai

Collaborators

University of Barcelona

Investigators

  • Principal Investigator: Maria Beltrán, BS Psych, Centre Besai

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 5, 2024

Primary Completion (Estimated)

June 30, 2025

Study Completion (Estimated)

December 30, 2025

Study Registration Dates

First Submitted

June 5, 2024

First Submitted That Met QC Criteria

June 21, 2024

First Posted (Actual)

June 25, 2024

Study Record Updates

Last Update Posted (Estimated)

November 18, 2024

Last Update Submitted That Met QC Criteria

November 15, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • BesaiBcn01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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