Status:
COMPLETED
Efficacy of a Sensory Comfort Room in Agitation Control
Lead Sponsor:
Bioaraba Health Research Institute
Conditions:
Mental Disorders, Severe
Eligibility:
All Genders
Phase:
NA
Brief Summary
In the initial approach of the study, it was considered that the comfort room would be used by all patients with GCT treated in the Functional Rehabilitation Area 1 (ARF 1) of the Álava Psychiatric Ho...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- All patients admitted to functional rehabilitation area 1 presenting with questionable, mild or moderate Agitation (score less than or equal to 20 on the PEC scale) or at the patient's request.
- To have freely accepted to participate in the intervention and to have signed the informed consent. An information sheet will also be given to the patient and an information sheet to the tutor (APPENDIXES 1 and 2). Experts in easy reading are consulted to adapt this document.
- Exclusion criteria:
- Severe and extremely severe agitation (score greater than or equal to 21 on the PEC scale). Immediate previous physical aggression.
- Declination of the signature of informed consent.
- Any participant who does not comply with the rules of use of the room will be excluded from the study.
Exclusion
Key Trial Info
Start Date :
May 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2023
Estimated Enrollment :
62 Patients enrolled
Trial Details
Trial ID
NCT06547671
Start Date
May 1 2021
End Date
May 1 2023
Last Update
August 9 2024
Active Locations (1)
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1
Araba University Hospital
Vitoria-Gasteiz, Alava, Spain