Clinical research on the feasibility of the contact detection sensor to prevent self-removal
Not Applicable
Recruiting
- Conditions
- Cognitive decline or dementiaD003704
- Registration Number
- JPRN-jRCT1030220494
- Lead Sponsor
- Amemiya Ayumi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Patients using physical restraint with cognitive decline who have a nasogastric tube, intravenous catheter, or oxygen tube attached and are at risk of self-removal
Exclusion Criteria
Patients who do not consent to participate in the study
Patients with unstable vital signs, patients
Terminally ill patients
Aggressive patients
Patients with delirium
Patients without family members
Patients receiving drugs that need to be adjusted in minute doses
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method