Anxiety Clinical Trial
— OCEANOfficial title:
Evaluation of a Comprehensive Approach in the Management of Anxiety in Intensive Care Unit Including Olfactotherapy
Verified date | November 2020 |
Source | Laboratoires Arkopharma |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The OCEAN observational study is a pilot study. The aim is to validate the interest of the intervention of essential oils, relaxing music and dim light on the anxiety of patient who are in the intensive care unit.
Status | Completed |
Enrollment | 35 |
Est. completion date | November 11, 2020 |
Est. primary completion date | November 11, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Hospitalized in one of the departments participating in the study - Presenting moderate to high intensity anxiety (Digital scale = 5); Exclusion Criteria: - Having already benefited from the "ZEN cart" - Having taken an anxiolytic during the past 48 hours - Patient (s) intubated and / or sedated - Allergy or known intolerance to one of the essential oils used - Respiratory allergies, asthma, or a history of seizures - Unable to understand the information note (linguistic reason, or related to his medical condition) - Pregnant or lactating woman. |
Country | Name | City | State |
---|---|---|---|
France | Institut Arnault Tzanck | Saint-Laurent du Var |
Lead Sponsor | Collaborator |
---|---|
Laboratoires Arkopharma |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | measurement of the evolution of anxiety | The main objective of this study is to measure the evolution of the patient's anxiety between H0 (start of a "ZEN cart" session) and H6 (end of the "ZEN cart" session). | 6 hours |
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