Trials / Completed
CompletedNCT03573843
Software-guided Cognitive Stimulation to Prevents Delirium
Cognitive Stimulation Guided by a Software to Prevent Delirium in Older Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- University of Chile · Academic / Other
- Sex
- All
- Age
- 65 Years
- Healthy volunteers
- Not accepted
Summary
This study is a pilot randomized controlled trial, comparing a group of older patients with standardized non-pharmacological delirium prevention plus a basic tablet versus a group with standardized non-pharmacological delirium prevention plus a tablet with a software of cognitive stimulation (PREVEDEL). Software:It is a local development, including a interprofessional team of delirium healthcare experts, older patients and a team og engineers. The software was developed during the first year of this project and was inscribed for author rights. Inclusion criteria: Older patients \> 65 y.o. Admitted to medicine room or intermediate care unit \> 48 hrs, and informed consent to participate. Exclusion Criteria:Delirium positive, neuroleptic use, dementia, and non-spanish speakers. The study was approved by ethical committee of Hospital Clinico University of Chile Standardized Non-pharmacological intervention: Health workers were previously educated in delirium, and environmental issues were implemented. This intervention coverage in nine different domains: orientation, early mobilization, environmental noise and light, sensorial deficit, sleep, hydratation, drug reduction, and family participation. Intervention: All patients will have a tablet with or without the software PREVEDEL between 09:00-19:00 hrs. Measures: delirium will be monitoring with CAM (Confusion Assessment Method) twice a day for 5 days. Primary outcome: Delirium rate between both groups Secondary outcomes:Long of stay, severity od delirium, time of use of electronic device, and Barthel to discharge.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Prevention software | All patients will have a tablet with the software PREVEDEL between 09:00-19:00 hrs. |
| OTHER | Placebo | All patients will have a tablet without the software PREVEDEL between 09:00-19:00 hrs. |
Timeline
- Start date
- 2018-06-15
- Primary completion
- 2018-08-31
- Completion
- 2019-10-30
- First posted
- 2018-06-29
- Last updated
- 2020-01-14
Locations
1 site across 1 country: Chile
Source: ClinicalTrials.gov record NCT03573843. Inclusion in this directory is not an endorsement.