CHU de Clermont-Ferrand
Clermont-Ferrand, 63000, France
NCT Number: NCT07482293
The primary objective of this study is therefore to propose and validate a French-language (France) version of the OHIP (49 questions) (OHIP-fr-49: long version), and the secondary objective is to validate a shortened version, OHIP-fr-14.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Clermont-Ferrand, 63000, France
When patients are admitted to the study center, if they are seeking periodontal treatment, they may be asked to participate in the study. The control group consists of patients meeting inclusion and exclusion criteria and agreeing to participate. Participants will complete the questionnaire during their visit (test). The same questionnaire will be re-administrated 15 days later to the first 50 patients in each group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Periodontitis group: patients with periodontitis requiring specific treatment
Control group: patients with at least 25 natural teeth and not suffering from periodontitis.
Exclusion criteria
Self-administration of the OHIP-49
Time frame: Baseline ; 15 days (if applicable)
Self administration of Oral Health Impact Profile questionnaire. The total score ranges from 0 to 196 (OHIP-49), with higher scores indicating worse oral health-related quality of life.
University Hospital, Clermont-Ferrand
Other
Acronym: OHIP
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