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An investigation of cold pressor pain in children (Part I)

Samuel LeBaron1, Lonnie Zeltzer, Debra Fanurik

  • 1University of Calgary Faculty of Medicine, Calgary, AlbertaCanada Division of Hematology / Oncology, Children's Hospital of Los Angeles, Division of Child Development and Biobehavioral Pediatrics U.C.L.A. School of Medicine, Los Angeles, CAU.S.A. University of Alabama, Tuscaloosa, ALU.S.A.

Pain
|May 1, 1989
PubMed

Insights

This study explored the cold pressor model for assessing pain in children. Results show it

Area of Science:

  • Pediatric pain research
  • Experimental psychology
  • Child well-being studies

Background:

  • The cold pressor test (CPT) is a common method for studying pain in adults.
  • Its application in pediatric populations is limited due to ethical considerations regarding child participants' well-being.
  • There is a need to adapt and validate pain assessment methods for children.

Purpose of the Study:

  • To evaluate the feasibility of conducting CPT in children (ages 6-12) in an engaging and non-threatening manner.
  • To determine if systematic and useful pain data can be collected using this model in a pediatric cohort.
  • To assess the perceived stress and engagement levels of children and their parents during the study.

Main Methods:

  • A pilot study was conducted with children aged 6-12 years.
  • Participants underwent arm immersion in cold water at 15°C (n=37) and 12°C (n=29).
  • Pain ratings were collected, and subjective feedback on the study's format was obtained from children and parents.

Main Results:

  • Children's pain ratings significantly increased with longer immersion durations and lower water temperatures.
  • The CPT paradigm yielded systematically obtainable and useful pain data in this pediatric sample.
  • Both children and their parents reported the study format as interesting and non-stressful.

Conclusions:

  • The cold pressor test can be adapted for pediatric research, yielding valuable pain data.
  • The method was perceived positively by child participants and their parents, indicating good feasibility.
  • Future pediatric pain studies using this model require continued ethical vigilance and refined well-being monitoring techniques.

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