Self-assessment of Olfactory Disorders for French Speaking Patients
VIF-DOR
Validation of Two Self-questinnaires on Olfactory Disorders for French Speaking Patients: the Self-evaluation of Olfactory Capacities and Quality of Life Questionnaires
1 other identifier
observational
135
1 country
1
Brief Summary
Sense of smell disorders are common and are said to affect up to 20% of the general population. They are often disabling and have a real impact on the quality of life. Smell disorders are most often assessed using a visual analogue scale and more rarely with objective tests (Sniffing Stick Test). Many ENT units do not have these objective tests because they are time-consuming and are not covered by health insurance. Some teams, such as that of Dr Thomas Hummel of the Carl Gustav Carus University Clinic in Dresden Germany, have developed self-assessment questionnaires for the sense of smell in order to improve the overall care of patients with olfactory disorders. Two of these self-questionnaires seem to us to be particularly relevant for use in everyday practice. Since then, these questionnaires have already been validated in different languages (English, Chinese, Korean...), but have never been translated and validated in French. Translating and validating these questionnaires into French would make it possible to improve the management and follow-up of French patients with olfactory disorders and to assess the impact of loss of smell on their quality of life.
Trial Health
Trial Health Score
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participants targeted
Target at P50-P75 for all trials
Started Jan 2021
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 8, 2021
CompletedFirst Posted
Study publicly available on registry
January 12, 2021
CompletedStudy Start
First participant enrolled
January 22, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 22, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
April 22, 2022
CompletedApril 18, 2023
April 1, 2023
1.2 years
January 8, 2021
April 14, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Reliability of the self-assessment questionnaire
To assess the reliability of the self-assessment questionnaire of his olfactory capacities (Self-MOQ) in French in patients presenting an olfactory dysfunction of any acquired etiology for more than 3 months using a test-retest trial.
3 months
Study Arms (2)
Case
Patient presenting an olfactory dysfunction of any acquired aetiology that has been evolving for at least 3 months without total recovery.
Control
Patient with no sense of smell problems followed up in ENT for another pathology that does not affect the sense of smell
Interventions
* Assessment of sense of smell or loss of smell using an Analogue Visual Scale * Carrying out the objective smell test (Sniffin' sticks test) (gold standard) * Information from two self-questionnaires translated into French: a quality of life questionnaire (The Questionnaire Olfactory Disorders (QOD)) and a self-assessment questionnaire of his olfactory capacities (Self-Mini Olfactory Questionnaire (Self-MOQ))
Eligibility Criteria
Case patients with acquired olfactory disorders will be selected from the ENT primary care clinic of Strasbourg University Hospital. Control patient without olfactory disorders are treated for another ENT pathology in the ENT primary care clinic of Strasbourg University Hospital.
You may qualify if:
- Patient \> 18 years old
- Patient affiliated to a sickness insurance social protection scheme, beneficiary or rightful claimant
- Patient who has not expressed his or her opposition to the collection and processing of his or her data for research purposes after the investigator has provided informed information.
- Patient presenting an olfactory dysfunction of any acquired aetiology that has been evolving for at least 3 months without total recovery (case group).
- Patient with no sense of smell problems followed up in ENT for another pathology that does not affect the sense of smell (control group).
You may not qualify if:
- Patient in an emergency or life-threatening situation
- Patient under judicial protection
- Patient under guardianship or trusteeship
- Inability to provide informed information to the patient (patient does not speak or understand French)
- Patient with congenital syndromic or non-syndromic congenital anosmia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Les Hôpitaux Universitaires de Strasbourg
Strasbourg, 67098, France
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 8, 2021
First Posted
January 12, 2021
Study Start
January 22, 2021
Primary Completion
April 22, 2022
Study Completion
April 22, 2022
Last Updated
April 18, 2023
Record last verified: 2023-04