NCT06839950Recruiting
Sensory Profile and Early Clinical Signs of Calm Room Users
Source: ClinicalTrials.gov · Last updated 30 Oct 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 80 (estimated)
- First submitted
- 12 Feb 2025
- Start date
- 19 Dec 2023
- Primary completion date
- 19 Dec 2027
- Lead sponsor
- Centre Hospitalier Esquirol
- NCT number
- NCT06839950
What you commit to
- Study type: Observational
- Planned participants: 80
- From 19 Dec 2023 to the primary completion date, 19 Dec 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous Participation in this research protocol (in the case of a new hospitalization)
Other illness
- Dementia
Other
- Inability to understand information related to the study
- Proven sensory disability
- Pregnancy
- Lack of social protection
- Expression abilities incompatible with completing the AASP Scale (e.g., french language comprehension issues, mute individuals, patients in restraint and/or therapeutic isolation)
Who the study is looking for
- 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).
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Esquirol Hsopital Center Coordinator of this site? Confirm its status | Limoges | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.