Facilitating Adaptive Expertise in Learning Computed Tomography (FAIL CT)
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ClinicalTrials.gov Identifier: NCT05284838 |
Recruitment Status :
Not yet recruiting
First Posted : March 17, 2022
Last Update Posted : March 17, 2022
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Condition or disease | Intervention/treatment | Phase |
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Adaptive Expertise Error Management Training | Other: Error Management Training (Difficult) Other: Error Management Training (Easy) Other: Error Avoidance Training | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 240 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | The FAIL CT Study: Facilitating Adaptive Expertise in Learning Computed Tomography, a Multi-center Randomized Controlled Trial |
Estimated Study Start Date : | July 2022 |
Estimated Primary Completion Date : | January 2023 |
Estimated Study Completion Date : | June 2023 |
Arm | Intervention/treatment |
---|---|
Experimental: Error Management Training (Difficult)
Participants receive the learning strategy Error Management Training and encounter difficult questions.
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Other: Error Management Training (Difficult)
Error Management Training is used to teach head computed tomography interpretation. Participants encounter difficult questions. |
Experimental: Error Management Training (Easy)
Participants receive the learning strategy Error Management Training and encounter easy questions.
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Other: Error Management Training (Easy)
Error Management Training is used to teach head computed tomography interpretation. Participants encounter easy questions. |
Active Comparator: Error Avoidance Training
Participants receive the learning strategy Error Avoidance Training.
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Other: Error Avoidance Training
Error Avoidance Training used to teach head computed tomography interpretation. |
- Percent correct on an assessment of transfer of skills [ Time Frame: Immediately after instructional session (up to 60 minutes to complete the assessment) ]Participants will have to demonstrate transfer of head computed tomography interpretation skills by interpreting novel radiology cases different from those used in the instructional session. Performance will be assessed by percent score on a head computed tomography interpretation test using novel radiology content not addressed in the instructional session. Score range is 0-100%.
- Percent correct on an assessment of post-session proficiency for learning objectives [ Time Frame: Immediately after instructional session (up to 60 minutes to complete the assessment) ]Participants will have to demonstrate direct application of the intervention's learning objectives by interpreting radiology cases similar to those used in the instructional session. Performance will be assessed by percent score on a head computed tomography interpretation test using radiology content similar to that used in the instructional session. Score range is 0-100%.
- Percent correct on an assessment of transfer of skills [ Time Frame: Three months after instructional session (up to 60 minutes to complete the assessment) ]Participants will have to demonstrate transfer of head computed tomography interpretation skills by interpreting novel radiology cases different from those used in the instructional session. Performance will be assessed by percent score on a head computed tomography interpretation test using novel radiology content not addressed in the instructional session. Score range is 0-100%.
- Percent correct on an assessment ofpost-session proficiency for learning objectives [ Time Frame: Three months after instructional session (up to 60 minutes to complete the assessment) ]Participants will have to demonstrate direct application of the intervention's learning objectives by interpreting radiology cases similar to those used in the instructional session. Performance will be assessed by percent score on a head computed tomography interpretation test using radiology content similar to that used in the instructional session. Score range is 0-100%.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Study participation will be available to all current emergency medicine residents at Stanford and at thirteen external sites.
Exclusion Criteria:
- Adults unable to consent
- Pregnant women
- Individuals who are not yet adults (infants, children, teenagers)
- Prisoners
- Medical students
- Residents from specialties other than emergency medicine

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): NCT05284838
Contact: Leonardo Aliaga, MD | 773-655-6705 | aliagal@stanford.edu |
Principal Investigator: | Leonardo Aliaga, MD | Stanford University |
Responsible Party: | Leonardo Aliaga, Clinical Instructor, Department of Emergency Medicine, Stanford University |
ClinicalTrials.gov Identifier: | NCT05284838 |
Other Study ID Numbers: |
64099 |
First Posted: | March 17, 2022 Key Record Dates |
Last Update Posted: | March 17, 2022 |
Last Verified: | March 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Plan Description: | No current plan to share data. |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |