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Radiation OncologyNCT06115811

Radiation Treatment Plan Evaluation Learning Tool Pilot Project

A study testing Radiation Treatment Plan Evaluation Learning Tool in people with Radiation Oncology, run by Massachusetts General Hospital at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Radiation Oncology
What is being tested?
Radiation Treatment Plan Evaluation Learning Tool
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteUnited States
Study dates
15 Jun 2026to 1 Jul 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • -The study will not include any special populations.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Rachel Jimenez, MD contact

617-726-8651

RBJIMENEZ@PARTNERS.ORG

United States1 site
  • Massachusetts General Hospital Cancer Center

    Boston, Massachusetts, 02215

    Rachel Jimenez, MD, 617-726-8651, RBJIMENEZ@PARTNERS.ORG

Other trials in United States

About this study

Official title: Development and Assessment of a Novel, Systematic Radiation Treatment Plan Evaluation Learning Tool for Radiation Oncology Residents

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.

Read the 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.

Being tested
Radiation Treatment Plan Evaluation Learning Tool
Keywords
Radiation Oncology, Education

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Radiation Treatment Plan Evaluation Learning ToolBehavioural

    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.

Study groups in NCT06115811
Study groupRoleWhat they receive
Radiation Treatment Plan Evaluation Learning ModuleExperimentalRadiation oncology resident physicians will complete study procedures as below: * Initial survey and pre-module examination. * Learning module. * Post-module survey and examination.
Receives: Behavioral: Radiation Treatment Plan Evaluation Learning Tool

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Objective Examination Score

    Analyzed with a paired samples t-test.

    Measured: Up to 8 weeks

Secondary outcomes (2)
  1. Oncology Resident Confidence Rate

    Scored using Likert scales and analyzed with non-parametric tests.

    Measured: Week 1 - 8

  2. Oncology Resident Perceived Competence Rate

    Scored using Likert scales and analyzed with non-parametric tests.

    Measured: Week 1 - 8

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Nov 2023
  2. Study start15 Jun 2026 (estimated)
  3. Primary completion15 Jun 2028 (estimated)
  4. Study completion1 Jul 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06115811
Sponsor's protocol ID
23-021
Status last verified
May 2026
First submitted
30 Oct 2023
Last updated
22 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The Dana-Farber / Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: \[contact information for Sponsor Investigator or designee\]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.

Questions about this trial

What is this clinical trial studying?

A study testing Radiation Treatment Plan Evaluation Learning Tool in people with Radiation Oncology, run by Massachusetts General Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 22 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Rachel Jimenez, MD (617-726-8651, RBJIMENEZ@PARTNERS.ORG), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Objective Examination Score (time frame: Up to 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 May 2026; AzTrials last refreshed its copy on 2 Nov 2026.

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