G43 G44.2
Conditions
Interventions
Group 1: Access to headache website after baseline survey T0 and until T3, exploring website using workbook (treatment group).
Group 2: Accessing headache website after final survey T3, exploring webs
Sponsors
Lehrstuhl für Kinderschmerztherapie und pädiatrische Palliativversorgung, Universität Witten/Herdecke
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Attendance of 5th or 6th grade at one of the participating schools, declaration of consent to study participation by a parent or guardian, consent to study participation by the adolescent, sufficient German language skills
Exclusion criteria
Exclusion criteria: Withdrawal of participation consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache-related disability (PedMIDAS adjusted for 30-day interval) assessed at 4 measurement time points: T0 (baseline), T1 (+1 month), T2 (+1 month), T3 (+1 month); primary endpoint is PedMIDAS at T3. All surveys take place electronically; T0 and T3 on tablet PCs; for T1 and T2 a link to an online questionnaire is sent by mail, which can be filled in across devices. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain intensity and frequency (PedMIDAS adjusted for 30-day interval), Pain Coping (PPCI-r; T0-T3), Headache-specific knowledge (Headache Knowledge Questionnaire; T0, T1, T3), Pain self-efficacy (S3; T0-T3). All surveys take place electronically; T0 and T3 on tablet PCs; for T1 and T2, a link to an online questionnaire will be sent by e-mail, which can be completed across devices. | — |
Countries
Germany
Contacts
Public ContactJulia Wager
Deutsches Kinderschmerzzentrum, Vestische Kinder- und Jugendklinik Datteln
Outcome results
None listed