Understanding sensory profiles of patients using a calming room
Official title: Sensory Profile and Early Clinical Signs of Calm Room Users
Run by Centre Hospitalier Esquirol · NCT06839950 · Data updated 2026-11-12
This study looks at how patients in a psychiatric hospital respond to different senses before and after using a calming room to see if their sensory experiences affect their mental health.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Centre Hospitalier Esquirol Academic / other |
| Locations | 1 site (Limoges, New Aquitaine) |
| Status | Recruiting |
| Started | December 19, 2023 |
| Main results expected | December 19, 2027 |
| Study ends | May 19, 2028 |
| Registry record updated | October 30, 2026 |
| Trial ID | NCT06839950 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are males and females aged 18 to 65 who are hospitalized in a closed unit for less than 10 days.
✕Probably not a fit
Patients with proven sensory disabilities, dementia, or those unable to comprehend study information may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to characterize the sensory profiles of patients in a closed psychiatric hospital unit who utilize a calming room. Participants will complete surveys before and after using the calming room to assess their sensory processing and identify potential links between sensory processing disorders and distress. The study seeks to determine if users exhibit extreme sensory profiles, either hypersensitivity or hyposensitivity, which may contribute to their mental health conditions.
Why it matters
Potential benefit: If successful, this study could enhance therapeutic approaches for patients with psychotic, personality, and mood disorders by tailoring interventions based on sensory profiles.
How similar studies have gone: While the approach of assessing sensory profiles in psychiatric settings is gaining interest, this specific study appears to be novel and untested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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). Exclusion Criteria: * Inability to understand information related to the study * Proven sensory disability * Dementia * Pregnancy * Lack of social protection * Previous Participation in this research protocol (in the case of a new hospitalization) * Expression abilities incompatible with completing the AASP Scale (e.g., french language comprehension issues, mute individuals, patients in restraint and/or therapeutic isolation)
Where it's running
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Esquirol Hsopital Center
Limoges, New Aquitaine, France Recruiting
Study contacts
- Study coordinator: Aude Paquet, PhD in Psychology
- Email: aude.paquet@ch-esquirol-limoges.fr
- Phone: +33 5-55-43-11-27
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.