Pain Burden in Children and Adolescents With Cerebral Palsy
A legfontosabb adatok
- Ki végzi
- Sykehuset Telemark
- Hol
- Saint Paul (Egyesült Államok)A helyszín megnézéseMég 4 másik országban, 4 helyszínen
- Azonosító
- Állapot
- Befejeződött
- Résztvevők
- 588 fő vett részt
- Kezdés
- 2020. márc. 12.
- Befejezés
- 2024. aug. 31.
- A vizsgálat típusa
- Megfigyeléses, 3 csoport
- A vizsgált kezelések
- Co-created intervention
- A regiszteradat frissítve
- 2024. október 16.
Ki vehet részt
- Életkor
- 0 év – 67 év
- Nem
- Nők és férfiak
- Egészséges önkéntesek
- Nem vehetnek részt
A regiszter feltételei, szó szerint
Mind a 6 feltétel megnézéseKevesebb
Ki vehet részt
- Children 0-18 years with a CP diagnosis registered in the Cerebral Palsy Registry of Norway (CPRN), or recruited through child habilitation centers, patient organizations or social media advertizing campains (USA, Canada, Finland \& Sweden)
- Siblings 12-18 years of a child/adolescent with CP (survey only)
- Clinicians identified by parents and/or children with CP as providers of pain-related care
Ki nem vehet részt
- Unable or unwilling to provide self-report
- Not able to communicate in English or Norwegian
- Lives with the child less than 50% of the time (parental interviews)
Helyszínek itt: Egyesült Államok
Még 4 másik országban, 4 helyszínen
- Gillette Children's Speciality HealthcareSaint Paul, Egyesült ÁllamokNo longer taking part
A vizsgálatról
Mit akar kideríteni a vizsgálat
Pain in children and adolescents with cerebral palsy (CP) is a significant health challenge that so far has received too little attention. We lack knowledge on how pain is experienced, its consequences and of perceived support in managing pain. The overarching aim of the CPPain-program is to reduce pain experience, pain interference (e.g. pain burden) in children and adolescents living with CP. CPPain has a prospective cohort comparative design and will include before- and after measurements and process evaluation of a nested intervention.
A teljes eredeti leírásKevesebb
This protocol concerns qualitative and quantitative data collection for the baseline of the CPPain program. The aim of the baseline data collection is to contribute in-depth knowledge of the pain burden in children and adolescents with CP. This knowledge is required to develop targeted pain-diminishing interventions in this vulnerable group of children with a high burden of challenges related to their chronic disease. In the next step, nested intervention will be co-created with children and adolescents with CP, their parents as well as health care professionals, and other professional caregivers involved in or responsible for management of pain based on existing research and baseline findings.
A vizsgálat 3 csoportja
- Children with a CP diagnosis
Children younger than 18 years with a CP diagnosis. Intervention will be determined later based on baseline results. Self- and/or proxy-reported survey and/or participation in interviews. Parents of all participants will provide proxy report. Children with CP \> 8 years of age and cognitively able (approx. 50%) will provide self-report.
Kezelés: Co-created intervention
- Controls
Siblings (12-17 years) of children with cerebral palsy. No intervention, self-reported survey.
- Health Care Professionals
Health Care Professionals identified as providers of pain care. No intervention, interview participants
Adatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- Hivatalos cím
- Pain and Pain Burden in Children and Adolescents With Cerebral Palsy - the CPPain Program
- A regiszteradat frissítve
- 2024. október 16.