Sensory Profile and Early Clinical Signs of Calm Room Users
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorCentre Hospitalier Esquirol
About this trial
This descriptive study aims primarily to characterize the sensory profile of patients in a closed psychiatric hospital unit who use a calming room.
The main questions it aims to answer are :
* Could sensory information processing disorders be the cause of distress and tension in these patients? * Could users of the calming room present extreme sensory processing profiles, characterized by either hypersensitivity or hyposensitivity ?
Participants will answer a survey to determine their the sensory profile. Participants can already use the calming room as part of their regular medical care and they will answer surveys before and after each use.
Eligibility criteria
Qualifiers
Gender and Age: Male or female, aged 18 to 65
Hospitalization: Admitted to the closed hospitalization unit for less than 10 days
Social security: Affiliated or beneficiary of a social security system
Consent: Free, informed, and written consent, signed by the participant and/or their legal representative (for participants under protection measures) and the investigator (at the latest on the day of inclusion and before any research-related examination).
Disqualifiers
Inability to understand information related to the study
Proven sensory disability
Dementia
Pregnancy
Trial design
Treatments tested in this trial
- Calm room
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov