Study Results
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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COMPLETED
NA
150 participants
INTERVENTIONAL
2018-08-28
2023-06-27
Brief Summary
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From all these observations, the hypothesis is that an olfactory training could improve the overall olfactory functioning and the emotional perception of the subjects presenting minor depressive symptoms and of the depressed patients.
Detailed Description
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The main objective is to study the effect of daily olfactory training on the emotional state and emotional perception of the subject. The effect of the training will be evaluated using three types of evaluations: (1) a clinical evaluation and the psychometric scales, (2) the investigation of the olfactory function and (3) the study of the emotional perception.
The secondary objectives are:
* The identification of olfactory parameters and emotional valences associated with minor depressive symptoms.
* The study of the link between the subjective and objective emotional response on the one hand, and the link between olfactory function, emotional perception and emotional state on the other hand in depressed patients and in individuals with minor depressive symptoms.
Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Sensory training
Sensory (Olfactory or visual) training will be done at home for 12 weeks.
The effect of the training will be evaluated using an experimental protocol includes (i) clinical and psychometric evaluations, (ii) the study of olfactory perception using Sniffin' Sticks Test and (iii) the study of the emotional perception using the "subjective" Sense'n Feel method and the "objective" measurement of the spontaneous pupillary dilatation.
Sensory training
12 weeks sensory training
Interventions
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Sensory training
12 weeks sensory training
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* QIDS scale score less than or equal to 15
* Affiliation to a social security system
* Able to give his written informed consent
* With a diagnosis of depressive episode characterized according to the DSM-5 criteria, confirmed by the Mini International Neuropsychiatric Interview (MINI)
* No argument for bipolar disorder or schizophrenia, confirmed by the MINI
* QIDS scale score greater than or equal to 16
* Follow-up in hospitalization and / or ambulatory consultation
* Without comorbidities (alcoholism, eating disorders ...)
* Affiliation to a social security system
* Able to give his written informed consent
Exclusion Criteria
* Allergies with one or more odors, food allergies and / or known anosmias and ageusia
* Legal incapacity and / or circumstances rendering the person incapable of understanding the nature, objectives or consequences of the study
18 Years
65 Years
ALL
Yes
Sponsors
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University Hospital, Tours
OTHER
Responsible Party
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Principal Investigators
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Wissam EL-HAGE, MD-PhD
Role: STUDY_DIRECTOR
University Hospital, Tours
Locations
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University health service, University ,Tours
Tours, , France
UMR 1253 IBrain, University, Tours
Tours, , France
University Psychiatric Clinic, University hospital,Tours
Tours, , France
Countries
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Other Identifiers
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2018-A00653-52
Identifier Type: OTHER
Identifier Source: secondary_id
2018.05.02
Identifier Type: OTHER
Identifier Source: secondary_id
PHAO17-WEH/ENOLFEA
Identifier Type: -
Identifier Source: org_study_id