- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06115811
Radiation Treatment Plan Evaluation Learning Tool Pilot Project
Development and Assessment of a Novel, Systematic Radiation Treatment Plan Evaluation Learning Tool for Radiation Oncology Residents
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study involves both the development of a novel learning tool, the Radiation Treatment Plan Evaluation Learning Module, as well as a pilot program to validate this tool as an effective resource to teach treatment plan review and optimization to radiation oncology residents.
Stud procedures include screening for eligibility and completion of surveys and oncology examinations.
Participation is expected to last about 6-8 weeks.
It is expected about 20 radiation oncology resident physicians will participate in the study.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rachel Jimenez, MD
- Phone Number: 617-726-8651
- Email: RBJIMENEZ@PARTNERS.ORG
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02215
- Massachusetts General Hospital Cancer Center
-
Contact:
- Rachel Jimenez, MD
- Phone Number: 617-726-8651
- Email: RBJIMENEZ@PARTNERS.ORG
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The pilot program will be open to radiation oncology resident physicians that are in their PGY-2, PGY-3, or PGY-4 year.
- All residents must have completed a breast cancer-specific radiation oncology rotation at least 3 months prior to enrollment in the pilot program in order to be eligible.
Exclusion Criteria:
-The study will not include any special populations.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Radiation Treatment Plan Evaluation Learning Module
Radiation oncology resident physicians will complete study procedures as below:
|
Web-based program comprised of a systematic, oncology treatment plan review system and learning modules.
The case bank of radiation treatments plans is accessible via econtour.org.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Objective Examination Score
Time Frame: Up to 8 weeks
|
Analyzed with a paired samples t-test.
|
Up to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oncology Resident Confidence Rate
Time Frame: Week 1 - 8
|
Scored using Likert scales and analyzed with non-parametric tests.
|
Week 1 - 8
|
|
Oncology Resident Perceived Competence Rate
Time Frame: Week 1 - 8
|
Scored using Likert scales and analyzed with non-parametric tests.
|
Week 1 - 8
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rachel Jimenez, MD, Massachusetts General Hospital
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23-021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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