Actively Recruiting

Age: 8Years - 17Years
All Genders
NCT05322018

Validation of Faces Thermometer Scale (FTS)

Led by Malmö University · Updated on 2025-05-18

150

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

Sponsors

M

Malmö University

Lead Sponsor

L

Lund University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this study is to evaluate validity and reliability of a novel digital pain measure tool, the Faces Thermometer Scale (FTS). Pain is commonly reported by children and adolescents undergoing dental treatment. Pain is also a strongly contributing factor in the development of Dental Fear and Anxiety (DFA). Professionals often underestimate the pain perceived by their patients. Self-report tools are seldom used to measure pain in a clinical setting, denying child patients the possibility to communicate their pain experiences. The aim of this study is to evaluate validity and reliability of a digital self-report pain measure tool, the Faces Thermometer Scale (FTS). Children and adolescents (N=150) aged 8 to 17 years visiting a dental clinic will be asked to score their pain using three different self-report pain tools; FTS, Faces Pain Scale-Revised (FPS-R) and Color Analog Scale (CAS). The validity and reliability of FPS-R and CAS is long established and will therefore be used to evaluate the psychometric properties of FTS.

CONDITIONS

Official Title

Validation of Faces Thermometer Scale (FTS)

Who Can Participate

Age: 8Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 8 and 17 years old and undergoing dental procedures and/or examinations
Not Eligible

You will not qualify if you...

  • Unable to understand Swedish or instructions on how to use the pain measurement tools

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Trial Site Locations

Total: 1 location

1

Malmö University

Malmö, Skåne County, Sweden, 205 06

Actively Recruiting

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Research Team

R

Rikard Roxner, PhDstudent

CONTACT

H

Henrik Berlin, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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