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NCT Number: NCT06390384

Prevention Programme for Improvement of Well-being and Level of Participation in Adolescents With Enhanced Psychiatric Burden in the School Environment.

The objectives of this two-arm phase-IIa randomized, controlled study are:

* to prove whether the combination of a clinic-guided personal counseling with a therapy-assistive digital support (blinded care approach) and a training of digital and mental health literacy is superior to a teacher-guided training of digital and mental health literacy only (treatment as usual) concerning the reduction of psychiatric burden in adolescents. * to improve the well-being and level of participation in adolescents at risk for psychiatric disorders. * to reduce the expression of psychiatric symptoms in adolescents with enhanced psychiatric burden. * to test whether the combination of a clinic-guided personal counseling with a therapy-assistive digital support is well accepted by students, their parents, and teachers. * to identify individual factors predicting the improvement of well-being and level of participation in adolescents as well as the acceptance of the prevention program in all subjects involved (students, parents, teachers, psychologists). * to investigate whether the clinic-guided personal counseling with a therapy-assistive digital support causes reduction of primary and secondary costs in the psychosocial support system and represents an economic advantage.

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Key information

Age range

10 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinic of Child and Adolescent Psychiatry, RWTH Aachen University

Aachen, North Rhine-Westphalia, 52074, Germany

Location contact

Anna Sotnikova, Dr.

CONTACT

Michael Siniatchkin, Prof. Dr.

CONTACT

About this study

The objectives of this two-arm phase-IIa randomized, controlled study are:

  • to prove whether the combination of a clinic-guided personal counseling with a therapy-assistive digital support (blinded care approach) and a training of digital and mental health literacy is superior to a teacher-guided training of digital and mental health literacy only (treatment as usual) concerning the reduction of psychiatric burden in adolescents.
  • to improve the well-being and level of participation in adolescents at risk for psychiatric disorders.
  • to reduce the expression of psychiatric symptoms in adolescents with enhanced psychiatric burden.
  • to test whether the combination of a clinic-guided personal counseling with a therapy-assistive digital support is well accepted by students, their parents, and teachers.
  • to identify individual factors predicting the improvement of well-being and level of participation in adolescents as well as the acceptance of the prevention program in all subjects involved (students, parents, teachers, psychologists).
  • to investigate whether the clinic-guided personal counseling with a therapy-assistive digital support causes reduction of primary and secondary costs in the psychosocial support system and represents an economic advantage.

The STEPS@SCHOOL clinical study is a two-arm parallel group phase-IIa randomized, non-blinded, controlled study with four measurement points (T1: confirming the risk status/checking inclusion criteria/informed consent; T2: baseline assessment and randomization prior to start of intervention; T3: post intervention assessment; T4: three months follow-up). The study will prove whether the combination of a clinic-guided personal counseling with a therapy-assistive digital support (first arm) is superior to a teacher-guided digital preventive platform with stand-alone digital applications (second arm, described as treatment as usual) concerning the reduction of psychiatric burden in adolescents. To prove this objective, a comparison between two groups (treatment of approval vs. treatment as usual) is necessary.

The intervention is a implementation of a weekly psychological counseling for psychiatric problems via videoconference combined with an additionally digital support using a well-established mobile treatment system STEPS®. The intervention will include: 1) digital and mental literacy training for children, parents and teachers in the school; 2) weekly counselling over 6 weeks via videoconference for adolescents and their parents; 3) blinded-care use of the mobile treatment system STEPS®.

Control condition (Treatment as Usual) includes the implementation of the digital and mental literacy training, however, no weekly counselling by the team of the clinic and no blinded-care use of the mobile treatment system STEPS®.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children and adolescents of both genders (w : m = 1 : 1) aged from 10 to 14 years
  • Psychiatric symptoms characterized using SDQ-25 with the cutoff > 17
  • Regular school attendence

Exclusion criteria

  • IQ <80, ongoing psychiatric or psychotherapeutic treatment with regular appointments (at least once a month).

Treatment and study plan

blinded-care counselling

Other

The intervention is a implementation of a weekly psychological counseling for psychiatric problems via videoconference combined with an additionally digital support using a well-established mobile treatment system STEPS®. The intervention will include: 2) weekly counselling over 6 weeks via videoconference for adolescents and their parents.

The counselling will be provided by experienced psychologists as employers of the Clinic of Child and Adolescent Psychiatry, RWTH Aachen University, the counselling will be supervised by the leading psychologist of the clinic. The counselling will include psychoeducative elements about psychological and psychosocial problems, behavioral interventions from cognitive-behavioral therapy, psychological techniques for better coping with stress, different therapeutic tasks such as fear exposure, activation exercises e.c. The students will be instructed to use the mobile treatment system STEPS in order to continue therapy at home.

App STEPS

Other

The intervention is a implementation of a weekly psychological counseling for psychiatric problems via videoconference combined with an additionally digital support using a well-established mobile treatment system STEPS®. The intervention will include: 3) blinded-care use of the mobile treatment system STEPS®.

This is transdiagnostic digital treatment system which consists of a students front-end as an App and a therapist front-end as an online platform. The App and the platform are connected to each other. In such a way, an effective data transter (for example, symptom evaluation by the student and tasks and requests by the therapist), direct communication between a student and a therapist, as well as registration of emergency situation, are possible.

digital and mental literacy training

Other

The intervention is a implementation of a weekly psychological counseling for psychiatric problems via videoconference combined with an additionally digital support using a well-established mobile treatment system STEPS®.

The intervention will include: 1) digital and mental literacy training for children, parents and teachers in the school.

This training program (4 weeks, 8 session a 2 lesson units, 2 sessions a week) includes information about rules and functions by using mobile applications, safety aspects of personal data, risks associated with data sharing, sexing and cybergrooming, managing social media, handling with fake news, influence of social media on mental health, forms of digital violence and strategies to cope with them.

Primary outcomes

  1. Student's well-being and level of participation

    Time frame: T2 (baseline) vs. T3 (post intervention assessment within one week); T2 (baseline) vs. T4 (3 months follow-up)

    Student's well-being and level of participation measured by KIDSCREEN-27.

Secondary outcomes

  1. Reduction of psychiatric burden

    Time frame: T2 (baseline) vs. T3 (post intervention assessment within one week); T2 (baseline) vs. T4 (3 months follow-up)

    Reduction of psychiatric burden as measured by SDQ-25, children/parent/teacher ) as well as SYMPTOM MONITORING as a daily individual symptom estimation on the likert scale in the Appversions.

  2. Reduction of children's global impairment

    Time frame: T2 (baseline) vs. T3 (post intervention assessment within one week); T2 (baseline) vs. T4 (3 months follow-up)

    Reduction of children's global impairment will be assessed by the the German version of the Chil-dren Global Assessment Scale.

  3. Feasibility measures

    Time frame: T2 (baseline) vs. T3 (post intervention assessment within one week); T2 (baseline) vs. T4 (3 months follow-up)

    Feasibility measures: number of students completed the programme, number of counselling ses-sions a student/parent, number of days/hours with STEPS support e.c..

Other outcomes

  1. Determinants and mediators

    Time frame: T2 (baseline)

    Acceptance of the App (UTAUT Questionnaire & Questionnaire according to the Theory of Planned Behavior)

  2. Determinants and mediators

    Time frame: T2 (baseline)

    Satisfaction with the program (ZUF-8 Zufriedenheitsfragebogen)

  3. Determinants and mediators

    Time frame: T2 (baseline)

    Resilience of children (RS-13)

  4. Determinants and mediators

    Time frame: T2 (baseline)

    Burden of parents (Parental Stress Scale)

  5. Determinants and mediators

    Time frame: T2 (baseline)

    Burden of parents (ENRICHD-social support instrument)

  6. Determinants and mediators

    Time frame: T2 (baseline)

    IQ (CFT 6-20R)

  7. Health economic aspects

    Time frame: T4 (3 months follow-up)

    The assessment of psychosocial and health care service use (as a basis for the estimation of treatment costs for the parents) will be performed by the German version of the Client Socioeconomic and Services Receipt Inventory (CSSRI-DE)

  8. Semi-structured interviews in the target populations

    Time frame: T4 (3 months follow-up)

    Semi-structured interviews in the target populations (patients, families, teachers, and health profes-sionals) will cover opinions, expectations, worries, beliefs, perceived benefits, risks, harms and dangers of the App, prevention programme, and digital literacy training. Particular attention will be paid to how target populations evaluate the introduction of the blinded-care treatment, and what benefits and problems they observed.

Study contacts

Contact information is provided by the study sponsor or research team.

Anna Sotnikova, Dr.

CONTACT

Michael Siniatchkin, Prof. Dr.

CONTACT

[email protected]

+49 241 80-89362

Sponsors and collaborators

Lead sponsor

RWTH Aachen University

Other

Registry information

Acronym: STEPS@SCHOOL

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Apr 30, 2024
Registry last updated
Apr 30, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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