Impact of a Snoezelen Element on Anxiety in Patients During Oral Care: A Real-Life Study at Nantes University Hospital
NCT ID: NCT06776653
Last Updated: 2025-01-15
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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NOT_YET_RECRUITING
100 participants
OBSERVATIONAL
2025-01-15
2025-03-15
Brief Summary
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The Snoezelen concept, developed in the 1970s, uses sensory stimulation (sight, sound, smell, and touch) to reduce anxiety. Initially designed for individuals with neurocognitive disorders, it creates a calming environment and has since been adopted in various healthcare settings.
At Nantes University Hospital, the dental department will test the Tovertafel Pixie®, a sensory projector designed to distract patients and reduce anxiety. Its mobility allows it to be used in waiting rooms and treatment areas, projecting onto ceilings, walls, or tables. This real-life study will assess whether patients exposed to the projector experience less anxiety compared to those who are not, with the goal of improving patient care and dental treatment experiences.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Tovertafel Pixie
Patients who will have the Tovertafel Pixie in the waiting room and the consultation room
Tovertafel Pixie
The Tovertafel Pixie® projector has a distracting effect, which can help divert the patient's attention while waiting for or undergoing treatment.
controle
Patients without the Tovertafel Pixie in the waiting room and the consultation room
No interventions assigned to this group
Interventions
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Tovertafel Pixie
The Tovertafel Pixie® projector has a distracting effect, which can help divert the patient's attention while waiting for or undergoing treatment.
Eligibility Criteria
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Inclusion Criteria
* consulting in the specialized care unit;
* who understands French;
* receiving care in the specialized dentistry unit and capable of expressing themselves independently regarding the various items in the questionnaire, whether orally, in writing, through a speech synthesis system, or using pictograms;
* able to provide consent to participate.
Exclusion Criteria
* refuse to participate in the study;
* under guardianship, curatorship, or legal protection.
18 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Isabelle Hyon, M.D
Role: PRINCIPAL_INVESTIGATOR
Nantes University Hospital
Central Contacts
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Other Identifiers
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AP_IH_IISLA_01
Identifier Type: -
Identifier Source: org_study_id
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