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Olfactory Training and Emotional State

Olfactory Training and Emotional State

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03605524
Acronym
ENOLFEA
Enrollment
150
Registered
2018-07-30
Start date
2018-08-28
Completion date
2023-06-27
Last updated
2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depressive Symptoms, Depressive Disorder, Major

Keywords

Sensory training, Depression, Olfaction, Emotion, Perception

Brief summary

During the past three decades, researchers have paid particular attention to the study of olfactory disorders in depression. Recent studies have shown that depression is characterized by a change in olfactory and emotional perception resulting in a decrease of the perception of positive stimuli (odors and facial expressions) and an increase in perception of negative stimuli (odors). Moreover, it has also been shown in healthy subjects that the presence of minor depressive symptoms leads to a decreasing of olfactory sensitivity. However, odor discrimination was not impaired in these subjects. This observation suggest the presence of a change in targeted olfactory perception in people with depressive symptoms without reporting major depression. In addition, studies in subjects with olfactory disorders (following respiratory tract infections or following Parkinson's disease) have shown an improvement in olfactory function after daily training with odors during 12 weeks. 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

Recent studies have shown that depression is characterized by a change in olfactory and emotional perception resulting in a decrease of the perception of positive stimuli (odors and facial expressions) and an increase in perception of negative stimuli (odors). Moreover, it has also been shown in healthy subjects that the presence of minor depressive symptoms leads to a decreasing of olfactory sensitivity. However, odor discrimination was not impaired in these subjects. This observation suggest the presence of a change in targeted olfactory perception in people with depressive symptoms without reporting major depression. In addition, studies in subjects with olfactory disorders (following respiratory tract infections or following Parkinson's disease) have shown an improvement in olfactory function after daily training with odors during 12 weeks. Therefore, 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. 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.

Interventions

12 weeks sensory training

Sponsors

University Hospital, Tours
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

healthy subjects: * Without psychiatric history * QIDS scale score less than or equal to 15 * Affiliation to a social security system * Able to give his written informed consent Inclusion Criteria depressed patients: * 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

healthy subjects and depressed patients: * Pathology or condition likely to modify their olfactory and / or taste perception * 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

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Olfactory Perception at 3 monthsBaseline (T0), a month and a half (T1.5), 3 months (T3)Score obtained with the Sniffin 'Stick test

Secondary

MeasureTime frameDescription
Emotional perception measured Sense'n Feel MethodBaseline (T0), a month and a half (T1.5), 3 months (T3)Score obtained with Sense'n Feel Method
Psychometric scale MINI : Psychiatric disorders explorationBaseline (T0), a month and a half (T1.5), 3 months (T3)Mini International Neuropsychiatric Interview
Psychometric scale TAS-20 : alexithymia assessmentBaseline (T0), a month and a half (T1.5), 3 months (T3)Twenty-item toronto Alexithymia Scale (TAS-20)
Emotional perception measured with SMI RED-m Scientific deviceBaseline (T0), a month and a half (T1.5), 3 months (T3)Observation of spontaneous pupillary dilatation with SMI RED-m Scientific device
Psychometric scale SHAPS : anhedonia assessmentBaseline (T0), a month and a half (T1.5), 3 months (T3)The Snaith-Hamilton Pleasure Scale
Psychometric scale QIDS-SR16 : Depression assessmentBaseline (T0), a month and a half (T1.5), 3 months (T3)Quick Inventory of Depressive Symptomatology
Psychometric scale STAI-Y : anxiety assessmentBaseline (T0), a month and a half (T1.5), 3 months (T3)State Trait Anxiety Inventory

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026