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Clinical Trials/NCT06776653
NCT06776653RecruitingNot Applicable

Impact of a Snoezelen Element on Anxiety in Patients With Special Needs During Oral Care at the Hôtel-Dieu University Hospital in Nantes: A Real-Life Study at Nantes University Hospital

Nantes University Hospital1 site in 1 country100 target enrollmentStarted: January 15, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
100
Locations
1
Primary Endpoint
Measurement of anxiety.

Study Overview

Brief Summary

Research on dental phobia highlights both external causes, like traumatic experiences or media influence, and internal factors, such as genetics and personality traits. While many studies focus on technical aspects of dental care, few explore how the care environment affects patient anxiety.

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.

Detailed Description

The study involves a questionnaire that the dental department usually provide to our patients, which is partially completed by the patient and partially by the practitioner at the end of the treatment session. No follow-up visit is required.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adult patient, over 18 years old;
  • •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

  • •receiving care in the specialized care unit who are unable to express themselves independently regarding the various items in the questionnaire, whether orally, in writing, through a speech synthesis system, or using pictograms;
  • •refuse to participate in the study;
  • •under guardianship, curatorship, or legal protection.

Arms & Interventions

controle

Patients without the Tovertafel Pixie in the waiting room and the consultation room

Tovertafel Pixie

Patients who will have the Tovertafel Pixie in the waiting room and the consultation room

Intervention: Tovertafel Pixie (Other)

Outcomes

Primary Outcomes

Measurement of anxiety.

Time Frame: 1 day

The Kleinknecht Dental Fear Survey (DFS) measures dental anxiety on a scale ranging from 20 (minimum) to 100 (maximum), where higher scores indicate greater levels of fear or anxiety - Comparison of means

Secondary Outcomes

  • Measure the waiting time in the waiting room(1day)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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