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Evaluation of Three School-based Mental Health Preventive Interventions in France

Effects of Three Prophylactic Interventions on French Middle-schoolers' Mental Health: Protocol for a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06059092
Enrollment
90
Registered
2023-09-28
Start date
2023-11-06
Completion date
2024-03-31
Last updated
2023-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emotional Distress, Functional Impairment, Psychosocial Problem, User Experience, Wellbeing

Keywords

Anxiety, Depression, Psychosocial adjustment, Emotional wellbeing, Social wellbeing, Psychological wellbeing

Brief summary

To meet adolescents' needs regarding mental health vulnerability, this study aims to propose and evaluate three original school-based preventive interventions delivered to French 13y-adolescents, with respect to their effects on mental health outcomes, as well as users' experiences of intervention, evaluated through questionnaires. Based on cognitive-behavioral therapies (CBT) techniques, these interventions target three strategic process areas: reactive adaptation, proactive adaptation, and interpersonal adaptation. Their effectiveness will be evaluated through a four-arm randomized controlled trial, conducted in an ecological context. Intra-group and inter-group comparisons will be carried out for our different variables of interest, namely targeted psychological processes, levels of distress, functional impairment, and well-being, and user experience indicators of acceptability, utility, and usability.

Detailed description

The three interventions will be delivered in school facilities, during school time, with 4th-grade middle school students, by one psychologist trained in CBT and one undergraduate student in clinical psychology in CBT. They involve participating in three one-hour weekly sessions, plus one booster sessions one month later. These three programs have been designed based on pre-existing knowledge about adolescents and their cognitive-motivational mechanisms, in order to promote their learning and receptiveness to interventions, and include group and individual activities meant to improve key psychological processes. The control group will consist of the same number of sessions of identical length as experimental conditions, dedicated to serious games meant to work on cognitive functions (attention, memory, logical reasoning). For all participants, several indicators of mental health and of cognitive-behavioral processes will be measured through validated self- and parent-reported questionnaires, and completed by user experience questionnaires. Mixt linear models or non-parametric equivalent tests will be conducted to test hypotheses (i.e., positive change in all outcomes following interventions in the experimental conditions, not observed in the participants of the control group). The interventions are preventive and will not target adolescents at risk for psychopathological conditions. Nevertheless, it is possible that at-risk individuals are enrolled in the sample. To meet special needs of some participants, from the beginning of the study, professional mental health resources (phone number, websites, institutions) will be provided to all participants. A clinical psychologist (one of tthe animator) will be available for students who would ask for individual appointments by handling duty periods in school facilities two hours a week during the interventions.

Interventions

BEHAVIORALAdapt Module

In each intervention, participants will be trained selected psychological skills using cognitive-behavioral-inspired techniques related to coping strategies, locus of control, coping metacognition, positive psychology strategies. Activities will involve brainstorming and exercises based on fictional situations, allowing active participation and reflection as well as feedback from animators and peers. Activities and aids have been designed to meet adolescents' developmental level, concerns and capacities and to support effective learning. Participants will be asked to carry out home tasks to practice learned skills. They will also be provided additional resources related to their module's thematic, accessible through a workbook and a website.

BEHAVIORALEngage Module

In each intervention, participants will be trained selected psychological skills using cognitive-behavioral-inspired techniques related to goal setting, planning, strengths identification, motivation; goal pursuit metacognition. Activities will involve brainstorming and exercises based on fictional situations, allowing active participation and reflection as well as feedback from animators and peers. Activities and aids have been designed to meet adolescents' developmental level, concerns and capacities and to support effective learning. Participants will be asked to carry out home tasks to practice learned skills. They will also be provided additional resources related to their module's thematic, accessible through a workbook and a website.

BEHAVIORALInteract Module

In each intervention, participants will be trained selected psychological skills using cognitive-behavioral-inspired techniques related to social cognition, assertive communication and conflict resolution, proactive prosocial behaviors, interactional metacognition. Activities will involve brainstorming and exercises based on fictional situations, allowing active participation and reflection as well as feedback from animators and peers. Activities and aids have been designed to meet adolescents' developmental level, concerns and capacities and to support effective learning. Participants will be asked to carry out home tasks to practice learned skills. They will also be provided additional resources related to their module's thematic, accessible through a workbook and a website.

BEHAVIORALControl Group

Sessions will be devoted to serious game training cognitive and executive functions through individual and group activities based on board games.

Sponsors

University of Nimes
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

Participants and their parents will not be aware of precise hypotheses. Nevertheless, for ethical reasons, they are informed that the interventions are meant to improve well-being (before random allocation to control or experimental conditions).

Intervention model description

A pre-test assessment will precede all interventions (experimental conditions) and control group sessions delivered simultaneously, and followed by a post-test assessment and and follow-up assessment three months after that.

Eligibility

Sex/Gender
ALL
Age
12 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* being enrolled in one of the middle school involved in the study * parent and student consent for participation * parent and student proficiency in French

Exclusion criteria

* absence or withdrawal of consent (parent or student) * missing more than 1 in 4 sessions

Design outcomes

Primary

MeasureTime frameDescription
Assertiveness in interactionPost-test 3 weeks after pre-test, follow-up 3 months after post-testAbility to express feelings and opinions to others and to respect others (Assertiveness Formative Questionnaire)
WellbeingPost-test 3 weeks after pre-test, follow-up 3 months after post-testPsychological, social and emotional well-being (Mental Health Continuum-Short Form). A high score on each emotional, social, and psychological wellbeing subscales, ranging from 3 or 6 to 18 or 36 depending on subscales, indicate a high level of each kind of wellbeing. A high composite score (ranging from 14 to 84) indicates a high level of general wellbeing.
Functional impairmentPost-test 3 weeks after pre-test, follow-up 3 months after post-testFunctional impairment in school, social, personal, domestic areas (Work and Social Adjustment Scale for Youth; WSAS-Y). A high score (ranging from 0 to 40) indicates a high level of functional impairment across these life areas.
Psychosocial difficultiesPost-test 3 weeks after pre-test, follow-up 3 months after post-testPsychosocial difficulties of various internalized and externalized natures, measured by the Pediatric Symptom Checklist (PSC). A high score (ranging from 0 to 70) indicates a high level of psychosocial difficulties.
Type of coping strategiesPost-test 3 weeks after pre-test, follow-up 3 months after post-testBrief-COPE. A high score on each of the 14 strategies subscales (e.g., denial, acceptance, planning, disengagement), ranging from 2 to 8, indicates a frequent use of each strategy.
Coping FlexibilityPost-test 3 weeks after pre-test, follow-up 3 months after post-testCoping Flexibility Scale. A high score (ranging from 7 to 28) indicates a high level of coping flexibility.
Tendency to engage in committed actionPost-test 3 weeks after pre-test, follow-up 3 months after post-testWillingness and Action Measurement for Children and Adolescents (WAM-C/a), Action subscales. A high score (ranging from 9 to 45) indicate a high tendency do carry out actions related to important personal values despite negative feelings.
General Self-EfficacyPost-test 3 weeks after pre-test, follow-up 3 months after post-testGeneral Self Efficacy scale-Short-form (S-GSES). A high score (ranging from 3 to 15) indicates a high level of general self-efficacy.
General distressPost-test 3 weeks after pre-test, follow-up 3 months after post-testAnxiety and depressive symptoms (Hospital Anxiety and Depression Scale). A high score on each subscale (anxiety symptoms subscale, 7 items, and depression symptoms subscale, 7 items), ranging from 0 to 21, indicates a high level of anxiety or depression. A high composite score (addition of scores yielded by the 2 subscales), ranging from 0 to 42, indicates a high level of general distress.

Secondary

MeasureTime frameDescription
Sociodemographic data 1Post-test 3 weeks after pre-test, follow-up 3 months after post-testAdolescents' gender (qualitative questionnaire, unscored)
Sociodemographic data 2Post-test 3 weeks after pre-test, follow-up 3 months after post-testAdolescents' age (questionnaire, unscored)
Sociodemographic data 3Post-test 3 weeks after pre-test, follow-up 3 months after post-testAdolescents' current and previous diagnoses and treatments qualitative (qualitative questionnaire, unscored)
Sociodemographic data 4Post-test 3 weeks after pre-test, follow-up 3 months after post-testFamily status (qualitative questionnaire, unscored)
Sociodemographic data 5Post-test 3 weeks after pre-test, follow-up 3 months after post-testHome income (questionnaire, unscored)
Sociodemographic data 6Post-test 3 weeks after pre-test, follow-up 3 months after post-testParents' gender, profession, education level (qualitative questionnaire, unscored)
User experience questionnairePost-test 3 weeks after pre-test, follow-up 3 months after post-testParticipants' perceived utility, acceptability, usability and general appreciation of the interventions

Countries

France

Contacts

Primary ContactEugenie Vaillant-Coindard, PhD Student
eugenie.vaillant-coindard@unimes.fr06 52 63 89 31
Backup ContactElodie Charbonnier, MCF HDR
elodie.charbonnier@unimes.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026