VAGABOND: a Mnemonic to Aid in the Memory Retention of the Canadian CT Head Rule
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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: NCT03565549 |
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Recruitment Status :
Completed
First Posted : June 21, 2018
Last Update Posted : March 31, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Traumatic Brain Injury Education | Behavioral: Mnemonic Behavioral: CCHR rule | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 100 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Masking Description: | Double |
| Primary Purpose: | Other |
| Official Title: | VAGABOND: a Mnemonic to Aid in the Memory Retention of the Canadian CT Head Rule for Patients With Minor Head Injury: A Randomized Controlled Trial on Interns and Senior Medical Students |
| Actual Study Start Date : | December 1, 2018 |
| Actual Primary Completion Date : | April 1, 2019 |
| Actual Study Completion Date : | September 1, 2019 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Mnemonic
Intervention group will receive a mnemonic aid to remember the CCHR
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Behavioral: Mnemonic
A mnemonic used as a memory aid |
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Active Comparator: CCHR rule
The control group will receive the CCHR only
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Behavioral: CCHR rule
A list of the CCHR items |
- memory retention of the Canadian CT Head Rule [ Time Frame: 6 months ]the effectiveness and usefulness of a simple one word mnemonic in the memory retention of the different components of the Canadian CT Head Rule
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: | 20 Years to 30 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- all final year medical students and interns
Exclusion Criteria:
- none
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): NCT03565549
| Oman | |
| Sultan Qaboos University | |
| Muscat, Oman | |
| Responsible Party: | Ammar Al Kashmiri, Senior consultant, Sultan Qaboos University |
| ClinicalTrials.gov Identifier: | NCT03565549 |
| Other Study ID Numbers: |
SultanQU |
| First Posted: | June 21, 2018 Key Record Dates |
| Last Update Posted: | March 31, 2020 |
| Last Verified: | March 2020 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Brain Trauma Medical education Emergency department |
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Brain Injuries Brain Injuries, Traumatic Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Craniocerebral Trauma Trauma, Nervous System Wounds and Injuries |

