Psycho-social Impact of Amelogenesis and Dentinogenesis Imperfecta

Brief Title

Psycho-social Impact of Amelogenesis and Dentinogenesis Imperfecta

Official Title

Psycho-social Impact of Amelogenesis and Dentinogenesis Imperfecta in Young People

Brief Summary

      The purpose of this research is to study the impact of dentinogenesis (DI) and amelogenesis
      (AI) imperfecta on oral quality of life, exposure to bullying and dental anxiety in a
      population of adolescents. We will use validated scales to evaluate the impact of bullying on
      the oral quality of live of youth aged 10 to 18 years, with non-syndromic DI or AI treated in
      seven national competence or reference centers in rare oral diseases.
    



Study Type

Observational


Primary Outcome

Child Oral Health Impact Profile (COHIP)


Condition

Dentinogenesis Imperfecta

Intervention

Questionnaires


Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Other

Estimated Enrollment

76

Start Date

June 2021

Completion Date

June 2023

Primary Completion Date

December 2022

Eligibility Criteria

        Inclusion Criteria:

          -  be between 10 and 18 years of age,

          -  consult in the O-Rare CRMRs of Strasbourg and Paris-Rothschild or the CCMRs of
             Bordeaux, Lyon, Marseille, Nantes, Toulouse for a care or follow-up consultation

          -  having a non-syndromic amelogenesis imperfecta or dentinogenesis imperfecta

          -  having access to a cell phone and/or tablet and/or personal or family computer

          -  covered by the social security of one of his parents

          -  understand French and one of whose parents (or legal representative) understands
             French

          -  have declared his or her non-opposition and one of whose parents (or legal
             representative) has declared his or her non-opposition to participate in the study.

        Exclusion Criteria:

          -  Child presenting for diagnostic consultation and child who cannot read or whose 2
             parents (legal representatives) cannot read
      

Gender

All

Ages

10 Years - 18 Years

Accepts Healthy Volunteers

No

Contacts

Emmanuelle Noirrit-Esclassan, 0561778378, [email protected]

Location Countries

France

Location Countries

France

Administrative Informations


NCT ID

NCT04927962

Organization ID

RC31/20/0255


Responsible Party

Sponsor

Study Sponsor

University Hospital, Toulouse


Study Sponsor

Emmanuelle Noirrit-Esclassan, Principal Investigator, University Hospital, Toulouse


Verification Date

June 2021