Clinical trial Recruiting at 1 site Interventional Ages 5 to 10

Distraction Methods to Ease Pain and Fear During a Child’s Blood Draw

Official title: Effects of Pinwheel Blowing, 3D Hologram Viewing, and Gum Chewing on Pain and Fear During Blood Draw in Children: A Randomized Controlled Trial

Run by Corlu State Hospital · NCT07770191 · Data updated 2026-11-12

This study tests if pinwheel blowing, a 3D hologram, or sugar-free gum can reduce pain and fear during blood draws for kids aged 5–10 compared with routine procedure.

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Quick facts

Study typeInterventional
Ages5 Years to 10 Years
SexAll
Enrollment164 (estimated)
SponsorCorlu State Hospital
Government
Locations1 site (Tekirdağ)
StatusRecruiting
StartedJune 15, 2026
Main results expectedSeptember 15, 2026
Study endsSeptember 15, 2026
Registry record updatedAugust 18, 2026
Trial IDNCT07770191 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are children aged 5–10 years scheduled for a blood draw, without recent analgesic use or sensory impairments, and whose guardians consent and children assent.

Probably not a fit

Children who do not experience significant distress from blood draws or who cannot complete the assigned distraction method may have limited benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This four-arm randomized trial compares active distraction (pinwheel blowing), visual distraction (3D hologram viewing), gustatory distraction (sugar-free gum chewing), and standard care during pediatric blood draws. Participants are children aged 5–10 years undergoing a blood draw, assigned equally to one of the four groups, with interventions starting one minute before and continuing through the procedure. Pain and fear are assessed by the child, a parent, and an independent nurse observer immediately after the draw. The study also measures parental satisfaction with the care provided during the procedure.

Why it matters

Potential benefit: If successful, these nonpharmacological distractions could lower pain and fear during blood draws and improve the overall experience for children and their families.

How similar studies have gone: Previous research has explored distraction during pediatric procedures with varying success; this study directly compares multiple distraction methods.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Children aged 5 to 10 years
* Scheduled to undergo a blood draw
* No analgesic medication use within 6 hours before the procedure
* No visual, hearing, or speech impairment
* No neurological disorder
* No oral or jaw condition that may prevent gum chewing
* No chronic illness requiring frequent invasive procedures
* Written informed consent provided by the parent or legal guardian
* Verbal assent provided by the children

Exclusion Criteria:

* Previous history of syncope during blood draw procedures
* Blood draw not completed on the first attempt
* Development of syncope during the procedure
* Inability or unwillingness to complete the assigned intervention
* Withdrawal of consent or assent by the parent or child at any stage of the study

Where it's running

  • Tekirdağ City Hospital
    Tekirdağ, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Gülsev Kutman — Tekirdağ City Hospital
  • Study coordinator: Gülsev Kutman, Rn Msc
  • Email: glsvktmn@gmail.com
  • Phone: 0905521392671

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.