Self-assessment of Olfactory Disorders for French Speaking Patients

NCT ID: NCT04705805

Last Updated: 2023-04-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

135 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-22

Study Completion Date

2022-04-22

Brief Summary

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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.

Detailed Description

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Conditions

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Post-viral Anosmia Post-traumatic Anosmia Chronic Rhinosinusitis Idiopathic Anosmia Age-related Loss of Smell

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Case

Patient presenting an olfactory dysfunction of any acquired aetiology that has been evolving for at least 3 months without total recovery.

Self-assessment of olfactory disorders through two questionnaires.

Intervention Type BEHAVIORAL

* 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))

Control

Patient with no sense of smell problems followed up in ENT for another pathology that does not affect the sense of smell

Self-assessment of olfactory disorders through two questionnaires.

Intervention Type BEHAVIORAL

* 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))

Interventions

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Self-assessment of olfactory disorders through two questionnaires.

* 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))

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 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).

Exclusion Criteria

* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Les Hôpitaux Universitaires de Strasbourg

Strasbourg, , France

Site Status

Countries

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France

Other Identifiers

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7917

Identifier Type: -

Identifier Source: org_study_id

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