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Survey for Parental Perception of Procedural Analgosedation in Pediatric Age.

Recruiting
Conditions
Analgesia
Sensation, Hyperalgesic
Registration Number
NCT06794879
Lead Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Brief Summary

The conduction of this study may provide useful information about how much parents know and understand about procedural sedation, helping to identify any gaps. In addition, expectations and concerns about procedural sedation may be highlighted so that strategies aimed at improving communication by health care personnel can be developed. The results may guide the development of training programs for health care personnel so as to improve the management of procedural sedation and interaction with parents.

Detailed Description

The study involves the completion of a survey by Parents/Guardians, the remaining interventions will be performed following the normal care procedure outpatient regimen, according to normal clinical practice.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
700
Inclusion Criteria
  • Parents of children between the ages of 2 months and 14 years who are afferent to the withdrawal clinic
Exclusion Criteria
  • None

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Identify the parent's degree of agreement/disagreement with pediatric procedural analgosedation practices and factors that may influence itthrough study completion, an average of 1 year

The parent's degree of agreement/disagreement with pediatric procedural analgosedation practices and the factors that may influence it will be analyzed by administering a survey

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

IRCCS Azienda Ospedaliero - Universitaria di Bologna

🇮🇹

Bologna, Italy

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