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Recruiting Observational

Promoting Children's Participation in Conventional X-ray Examinations

NCT06322264 · tracked via the Priya Life Science Sweden tracker
Phase
Observational
Started
2024-11-05
Last updated
2026-09-03

Condition(s) studied

Heart Rate DeterminationPatient Participation

Investigational drug(s) / intervention(s)

Measurement of variation in heart rate

Measurement of variation in heart rate: The children will be given a portable device that will monitor their heart rate, enabling the recording of the rate of their pulse.

Study summary

The goal of this explorative observational study is to map the procedure and child centered approach in the examination for children that undergo conventional X-ray examinations. The main questions aim to answer:

* How many images need to be retaken during conventional X-ray examinations?
* What is the reason why the pictures need to be redone?
* What is the time required for the various examinations?
* What experience of the procedure of the examination is there among those involved?
* Can the physical impact be observed through variation in heart rate in children that undergo conventional X-ray examinations?

Participants will answer questionnaires about the children's participation in the procedure and the variation in heart rate will be measured on the children who undergo the examinations.

Eligibility

Sex
ALL
Min age
4 Years
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * Children ages 4-12 yrs who undergo standard x-ray examinations * parents to the child * assigned radiographers Exclusion Criteria: * Children and parents who have cognitive and/or language difficulties

Primary outcome measure(s)

  • Variation in heart rate — The measurement is done through the examination total time 15 minutes (baseline before start 1-2 minutes, start of exam 2-10 minutes, end of exam after 10-15 minutes)
    To compare the variations in pulse with the experience of the examination

Trial sites (1)

FacilityCityRegionStatus
SUS Lund Skåne County Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06322264 on ClinicalTrials.gov ↗ ← All trials in Sweden