Education for Recognition and Management of Delirium
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03642249 |
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Recruitment Status :
Completed
First Posted : August 22, 2018
Last Update Posted : March 30, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Delirium Intensive Care Unit Syndrome Nurse-Patient Relations | Behavioral: OSCEs Behavioral: Lecture Behavioral: E-learning | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 72 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Investigator) |
| Primary Purpose: | Health Services Research |
| Official Title: | Evaluating the Effects of Implementing an Scenario-based Education Initiative and OSCE for Recognition and Management of Delirium in Adult Intensive Care Unit: Randomised Controlled Trial |
| Actual Study Start Date : | November 5, 2019 |
| Actual Primary Completion Date : | December 24, 2019 |
| Actual Study Completion Date : | December 31, 2019 |
| Arm | Intervention/treatment |
|---|---|
Experimental: experimental group
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Behavioral: OSCEs
Scenario-based education intervention, including objective structured clinical examinations (OSCEs) Behavioral: Lecture Face-to-face Education using Delirium Care Flip Chart Behavioral: E-learning Including 7 parts of delirium care video |
Active Comparator: control group
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Behavioral: Lecture
Face-to-face Education using Delirium Care Flip Chart Behavioral: E-learning Including 7 parts of delirium care video |
- Change from Baseline Delirium Knowledge and Skills at the time Immediately after the intervention and Six weeks [ Time Frame: T0(Baseline), T1(Immediately after the intervention), T2(Six weeks after the intervention) ]Delirium Knowledge and Skills Test (included 18 questions)
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Registered nurse worked in acute care unit and care with critical patients
- Licensed physician which undertake the post graduate year program worked in acute care unit and care with critical patients
Exclusion Criteria:
- Unwilling to involved the research
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03642249
| Taiwan | |
| Wan Fang Hospital | |
| Taipei, Taiwan, 116 | |
| Study Director: | Kee-Hsin Chen, PhD | Taipei Medical University |
| Responsible Party: | Taipei Medical University |
| ClinicalTrials.gov Identifier: | NCT03642249 |
| Other Study ID Numbers: |
N201803104 |
| First Posted: | August 22, 2018 Key Record Dates |
| Last Update Posted: | March 30, 2020 |
| Last Verified: | September 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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delirium knowledge translation Objective Structured Clinical Examination evidence-based practice |
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Delirium Confusion Neurobehavioral Manifestations Neurologic Manifestations |
Nervous System Diseases Neurocognitive Disorders Mental Disorders |

