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Indicated stress-prevention in adolescence

Indicated stress-prevention in adolescence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012778
Enrollment
80
Registered
2017-08-10
Start date
2017-10-02
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Stress Burnout

Interventions

Group 1: Interventiongroup: Participation in the training "Indizierte Stressprävention: Eine Akzeptanz- und Commitment-Therapiegruppe mit Jugendlichen" (engl.: "Indicated stress prevention: An Accepta
Werner, Kellenbenz & Kaess, 2017, unpublished manual): 8 units lasting 90 minutes each within 10 weeks. Each group consists of a maximum number of 10 participants and is led by two psychologists. Gro

Sponsors

Sektion für translationale Psychobiologie in der Kinder- und Jugendpsychiatrie, Klinik für Kinder- und Jugendpsychiatrie, Zentrum für Psychosoziale Medizin, Universitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 18 Years

Inclusion criteria

Inclusion criteria: Students attending year 8 to 12 at regular schools in the Rhine-Neckar-Region; increased level of stress (rawscore of 8 or higher in the Perceived Stress Scale-4 (Cohen et al., 1983). Only for the analysis of hair cortisol: Hair length at least 3 cm.

Exclusion criteria

Exclusion criteria: Current severe psychological disorder (Schizophrenia, Severe Major Depression, Borderline-Personality-Disorder), current psychotherapeutical treatment. For the analyis of hair cortisol (no requirement for the participation in the study in general): ingestion of drugs containing glucocorticoid or psychiatric drugs, pregnancy, endocrinologic or neurologic deseases. For the examination of the heart rate variability: cardiac arrhythmia.

Design outcomes

Primary

MeasureTime frame
Perceived stress measured via Perceived Stress Scale 10 (Cohen, Kamarck, & Mermelstein, 1983) at t1 (Postline), which is collected within four weeks after the end of the training of the intervention-group. The control-group did not receive training yet at this time.

Secondary

MeasureTime frame
Momentary perceived stress compared between intervention group and control group at the postline data collection. Symptoms associated with stress compared between intervention group and control group at the postline data collection measured by the School Burnout Inventory (Salmela-Aro, Kiuru, Leskinen & Nurmi, 2009) at the postline data collection. Hair cortisol and heart rate variability compared between intervention group and control group at the postline data collection. Physical symptoms caused by stress measured by the Children´s Somatization Inventory (Walker, Beck, Garber, & Lambert, 2009) compared between intervention group and control group at the postline data collection. Psychological flexibility Children´s Somatization Inventory (Walker, Beck, Garber, & Lambert, 2009) measured by the Acceptance and Fusion Questionnaire for Youth (Greco, Lambert, & Baer, 2008) at the postline data collection. Health-related quality of life measured by KIDSCEEN-10 (Ravens-Sieberer et al., 2005) at the postline data collection.

Countries

Germany

Contacts

Public ContactFranziska Binder

Klinik für Kinder- und Jugendpsychiatrie, Zentrum für Psychosoziale Medizin, Universitätsklinikum Heidelberg

franziska.binder@med.uni-heidelberg.de+49 6221 5634611

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026