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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02978352
Other study ID # 300/2559(EC4)
Secondary ID
Status Completed
Phase N/A
First received November 21, 2016
Last updated June 22, 2017
Start date January 2017
Est. completion date March 2017

Study information

Verified date June 2017
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Delirium is an acute and fluctuating disturbance of consciousness characterized by reduced attention, impaired cognition and perception, usually resulting from general physical conditions. Delirium contributes to longer hospital length of stay, increased mortality, increased healthcare costs, and long-term cognitive and functional impairment. However, it is often underdiagnosed and undertreated. E-learning (electronic learning) proves to be a time-efficient, flexible and convenient training method, making it suitable for a large organization like Siriraj hospital where there is a large employee turnover rate. So the investigators want to compare the passing rate between the e-learning group and the traditional learning group.


Description:

Primary objective: Compare the passing rate between the e-learning group and the traditional learning group

Secondary objectives: Assess the trainees' satisfaction and problems associated with e-learning implementation, Investigate the causes of inaccurate CAM-ICU assessment for improvement in future training sessions


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ICU nurse

- general ward nurse

- private ward nurses

- nurse anesthetists

Exclusion Criteria:

- Previous exposure to CAM-ICU

- Inability to complete the training courses

- Inability to complete the required 3 simulated patient scenarios

Study Design


Related Conditions & MeSH terms


Intervention

Other:
learning


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Outcome

Type Measure Description Time frame Safety issue
Primary The passing rate between the e-learning group and the traditional learning group 2 weeks
Secondary Assess the trainees' satisfaction Satisfaction score from 0 (dissatisfy) and 10 (very satisfy) 2 weeks
Secondary Investigate the causes of inaccurate CAM-ICU assessment for improvement in future training sessions 2 weeks
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