A Pilot study to assess PreSense system in improving turn-protocol compliance
Phase 3
- Conditions
- Health Condition 1: null- Pressure Ulcers
- Registration Number
- CTRI/2018/02/011713
- Lead Sponsor
- Healthcare Technology Innovation Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
All adults admitted to Intensive Care Unit (ICU) who are considered at risk of acquiring
pressure ulcers can be enrolled in the study.
Exclusion Criteria
1. Patients who cannot have the wearable device attached to their chest.
2. Patients who currently have implantable cardiovascular- defibrillator or pacemaker.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the current rate of compliance with prescribed turning protocols by using the system <br/ ><br>proposed and to compare it with the compliance rate prior to introduction of the system proposed.Timepoint: On completion of pilot study
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil