Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT07290725

Cross-cultural Adaptation and Translation Validation of the iADH Universal Case Mix Tool (UCMT).

This study aims to translate, culturally adapt, and validate the iADH Universal Case Mix Tool (UCMT) for dental care professionals working with people with disabilities.

The study will assess linguistic accuracy, applicability, and reliability/validity of the German, Spanish and Portuguese version of the instrument.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Conditions

Sex eligibility

All sexes

Study type

Observational

Primary location

SFU - Online questionnaire

Vienna, State of Vienna, 1020, Austria

About this study

This study is a multicentre, non-interventional methodological study aimed at translating, culturally adapting, and validating the iADH Universal case mix tool (UCMT) for use by dental care professionals working with people living with disabilities, following international guidelines for cross-cultural adaptation of measurement instruments. The translation and cultural adaptation process will include forward and backward translations of the original UCMT (English) to German, Spanish and Portuguese. Two independent forward translations will be performed for each language, followed by reconciliation into a single version, based on semantic equivalence, clarity and cultural appropriateness. Blinded backward translations into English will then be conducted to ensure conceptual consistency with the original instrument. A panel of experts, composed of dental experts and linguistic professionals fluent in both languages will review all translated versions using a Delphi approach. Later, the adapted instruments will be reviewed by the original UCMT developers for the final approval. Consent Validity Index (CVI) of the translated UCMT will be evaluated through expert ratings and cognitive interviews with dental professionals experienced in special care dentistry. Following the experts' validation, a pilot reliability phase will be conducted using standardised online clinical cases developed for the original versions of the UCMT. Participating raters will complete an online questionnaire using the translated UCMT. Intra and interrater agreement will be assessed to evaluate consistency of the translated instrument in a simulated clinical scenario. This study does not involve real patients of the collection of sensitive personal data.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Special care dentist
  • Native in German, Spanish or Portuguese
  • Agree to participate, complete the instrument 2 times

Exclusion criteria

  • Not meeting the inclusion criteria

Treatment and study plan

Primary outcomes

  1. Content validity of the translated UCMT

    Time frame: 1 week

    Content validity of the UCMT will be assessed by a panel of multidisciplinary experts, assessing clarity, relevance and cultural appropriateness. Experts ratings will be used to calculate Content Validity Index (CVI) for the translated versions of the UCMT. Unit of measure: CVI (Range 0-1)

Secondary outcomes

  1. Interrater agreement of the UCMT domains scores

    Time frame: 1 month

    Interrater agreement will be assessed based on scores assigned to the seven domains of the UCMT in the original version and validation. Raters will independently evaluate standardised online cases using the translated versions of the UCMT. Agreement between raters will be quantified for each UCMT domain.

    Unit of measure:

    Interclass correlation coefficient (range 0-1)

  2. Temporal stability (Test-retest) of UCMT domain scores

    Time frame: 2 weeks

    Intrarater agreement (Temporal stability) will be assessed based on scores assigned to the seven domains of the UCMT in the original version and validation. Raters will independently evaluate standardised online cases using the translated versions of the UCMT on two occasions separated by 1-2 weeks . Agreement between these occasions will be quantified for each UCMT domain.

    Unit of measure:

    Interclass correlation coefficient (range 0-1)

Sponsors and collaborators

Lead sponsor

Sigmund Freud PrivatUniversitat

Other

Collaborators

  • University of Chile
  • University of Freiburg

Registry information

Acronym: CCV UCMT

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Dec 18, 2025
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.