Oral Health Related Quality of Life (OHRQoL)
Conditions
Keywords
OHIP, oral health impact profile, quality of life, oral health, french version, OHIP 14, OHIP 49
Brief summary
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.
Detailed description
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.
Interventions
OTHEROHIP
Self-administration of the OHIP-49
Sponsors
University Hospital, Clermont-Ferrand
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
All participants (n=200) will be asked to complete OHIP questionnaire at the end of their scheduled visit for periodontal treatment or follow-up. The duration fullfilment is estimated at 10 minutes. The same questionnaire will be re-administered 15 days later at visit 2 (Retest), to one in two patients (n=100). If a second visit to the dental clinic is not necessary for the overall treatment plan, patients will be able to complete a paper questionnaire at home and return it by postal mail using a pre-stamped envelope or electronically (scanned questionnaire returned by e-mail).
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients aged 18 years or older * Native French speakers * Able to read and complete a questionnaire * Willing to take part in a study assessing perceived oral health Periodontitis group: patients with periodontitis requiring specific treatment Control group: patients with at least 25 natural teeth and not suffering from periodontitis.
Exclusion criteria
* Pregnant or breastfeeding patients; * Patients under guardianship, curatorship, or judicial protection * Patients deprived of their liberty * Patients participating in another clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Questionnaire OHIP-fr | 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. |
Countries
France
Contacts
PRINCIPAL_INVESTIGATORSophie Doméjean
CHU de Clermnt-Ferrand
Outcome results
None listed