Skip to main content
Clinical Trials/NCT07402837
NCT07402837Enrolling By InvitationNot Applicable

Creating a Flexible Curriculum Tool for Pediatric Palliative Care Rotating Learners

Children's National Research Institute1 site in 1 country30 target enrollmentStarted: January 1, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Response to the question "I achieved the standard objectives of the palliative care rotation."

Study Overview

Brief Summary

The goal of this clinical trial is to learn if a new educational tool can improve the training and educational process for learners who will already be taking part in the palliative care rotation at Children's National Hospital. The main questions it aims to answer are:

  • If learners who are trained using the educational tool more frequently answer strongly agree/agree to the question "I achieved the standard objectives of the palliative care rotation"
  • If learners who are trained using the educational tool more frequently answer strongly agree/agree to the question "I achieved my specific objectives of the palliative care rotation"

If there is a comparison group: Researchers will compare responses from learners who did and and did not have their rotation guided by the educational tool to see if there are differences.

Participants will engage in their palliative care rotation as they would have otherwise, though those in the intervention group will be provided different resources. They will be asked to provide responses to survey questions on their end-of-rotation evaluation, and some will be invited to participate in a focus group at the end of their rotation.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • must be an adult, greater than or equal to 18 years old
  • must have rotated with the pediatric palliative care team for at least 1/2 day during the study period
  • must speak English

Exclusion Criteria

  • there are no exclusion criteria for this study

Arms & Interventions

Control - Standard Education

Active Comparator

This is the standard palliative care education that most learners receive.

Intervention: Standard Palliative Care Education (Behavioral)

Intervention - Education Using Flexible Curriculum Tool

Experimental

This is the education using a new educational tool that tailors resources, guidance, and education to learner objectives, level of training, learning style, and palliative care experience.

Intervention: Rotation Using Flexible Education Tool (Behavioral)

Outcomes

Primary Outcomes

Response to the question "I achieved the standard objectives of the palliative care rotation."

Time Frame: Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt

Measured using Likert scale with 5 choices, 1 meaning Strongly Disagree, 5 meaning Strongly Agree

Secondary Outcomes

  • Response to the question "I achieved my specific objectives of the palliative care rotation."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "I was provided with a variety of resources to meet my learning objectives."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "The education I received matched my level of training."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "The education was appropriate to my previous exposure to hospice and palliative medicine."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "The education on this rotation matched my learning style."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "This rotation was valuable."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "The clinical educators promoted an open, respectful, and safe environment for discussion, learning, and improvement."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)
  • Response to the question "I would recommend this rotation to other learners."(Measured on an evaluation survey sent to participants within 2 weeks after the last day of their rotation, response due within 4 weeks after receipt)

Investigators

Sponsor
Children's National Research Institute
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nimisha Bajaj

Co-Principal Investigator

Children's National Research Institute

Study Sites (1)

Loading locations...

Similar Trials

Creating a Flexible Curriculum Tool for... | Clinical Trial