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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05285254
Other study ID # 21-002328
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 28, 2021
Est. completion date July 30, 2021

Study information

Verified date March 2022
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to provide the first systematic evidence that Certified Child Life Specialists reduce pain during vaccine administration and improve caregiver visit satisfaction in the pediatric primary care setting.


Recruitment information / eligibility

Status Completed
Enrollment 126
Est. completion date July 30, 2021
Est. primary completion date July 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 12 Years
Eligibility Inclusion Criteria: - Children 4-12 years of age presenting to MCHS Red Wing for a well child examination and vaccine administration. - Parents or caregivers of any age presenting to well child examination with child. - Legal guardians of all participants must provide verbal consent. - Patients must provide verbal assent for participation.Verbal assent will be waived for children younger than 6 years. Exclusion Criteria: - Children with autism or other severe developmental disabilities. - Children must be able to communicate pain before and after vaccine administration using the FPS-R.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Certified Child Life Specialist Support
Provides psychosocial care to children and families confronting stressful and painful situations

Locations

Country Name City State
United States Mayo Clinic Health System - Red Wing Red Wing Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient-reported pain Measured using the Faces Pain Scale-Revised (FPS-R). This is a self-report measure of pain validated for children ages 4-16 years of age and approved for the assessment of pediatric pain at Mayo Clinic. The scale utilizes different faces to score the sensation of pain on a 0-to-10 metric. Post vaccine administration, approximately 1 hour
Primary Observed Negative Emotional Responses Measured using the Children's Emotional Manifestation Scale (CEMS). The CEMS consists of five categories (facial expression, vocalization, activity, interaction, and level of cooperation) with each category scored from 1 to 5, with summed scores from 5 to 25. Higher scores represent more negative emotional behaviors. The scale was initially validated for children 7-12 years of age but has been subsequently used by other studies for children as young as 4 years of age. Post vaccine administration, approximately 1 hour
Secondary Caregiver visit satisfaction Measured by a caregiver satisfaction survey. This is a self-report 6-item survey to rate satisfaction level during child's immunization on a scale of 1=very satisfied and 5=dissatisfied. Post vaccine administration, approximately 1 hour
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