- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01707212
Prenatal Education About Infant Immunization Pain Management
26. oktober 2013 opdateret af: Anna Taddio, University of Toronto
A Prenatal Education Module for Parents to Improve the Use of Pain-management Strategies for Immunization in Two-month Old Infants: a Randomized Controlled Trial of Knowledge Translation
There are numerous pain management strategies available for the management of infant immunization pain.
The majority of infants, however do not benefit from these interventions, which causes them to suffer pain unnecessarily.
This study will assess the impact of educating parents about pain management strategies on their knowledge and behaviour regarding pain management during routine 2-month infant immunization injections.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
There is ample literature outlining effective pain management strategies for immunization including psychological, physical and pharmacological interventions; however their use in clinical practice has been limited.
Teaching parents about these strategies in an enriching setting such as prenatal education classes has the potential to increase utilization of these strategies, and empower parents to take on a more active role in the management of their infant's pain during routine immunization.
Educating parents about pain-management for infant immunization has not been previously investigated in this setting.
The aim of this cluster-randomized controlled trial is to evaluate the effectiveness of an immunization pain-management education module added to the prenatal education program at Mount Sinai Hospital on parental knowledge and behaviour regarding pain management during routine 2-month infant immunization injections.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
197
Fase
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Ontario
-
Toronto, Ontario, Canada, M5G 1X5
- Mount Sinai Hospital
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
16 år og ældre (Barn, Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- mothers attending weekend prenatal classes
- delivery of a healthy newborn > 35 weeks gestational age
- available for followup for infant's 2-month immunization
Exclusion Criteria:
- mothers who do not plan to immunize their infants
- infant with major birth defect or hospitalized at time of immunization
- mothers who need to attend the prenatal class at a separate time when education not offered
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Pain management education
Education about pain management during infant immunization
|
Education about pain management during infant immunization
|
|
Andet: No pain management education
Control - general information about immunization only
|
Control - no education about pain management during infant immunization
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Utilization of pain management strategies during infant immunization
Tidsramme: within 2 months of immunization
|
Parents will self-report utilization of specific pain management strategies during routine 2-month infant immunization
|
within 2 months of immunization
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Attempted use of pain management strategies during infant immunization
Tidsramme: within 2 months of immunization
|
Parents will self-reported attempted utilization of specific pain management strategies at 2-month infant immunization
|
within 2 months of immunization
|
|
Knowledge
Tidsramme: within 2 months of immunization
|
Parents will answer questions regarding their knowledge about the effectiveness of various pain management strategies for infant immunization injections
|
within 2 months of immunization
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Infant pain during immunization
Tidsramme: within 2 months of immunization
|
Parents will self-report infant pain during 2-month immunization using an 11-point Numerical Rating Scale (NRS)
|
within 2 months of immunization
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. oktober 2012
Primær færdiggørelse (Faktiske)
1. juli 2013
Studieafslutning (Faktiske)
1. juli 2013
Datoer for studieregistrering
Først indsendt
11. oktober 2012
Først indsendt, der opfyldte QC-kriterier
11. oktober 2012
Først opslået (Skøn)
16. oktober 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
29. oktober 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
26. oktober 2013
Sidst verificeret
1. oktober 2013
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 12-0134-E
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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