Recruiting soon

CARE-ONCBurnout Prevention Program for First-Year Medical Oncology Residents

Study Aim

This study aims to prevent burnout among first-year medical oncology residents by evaluating their emotional exhaustion, depersonalization, and personal accomplishment using the Maslach Burnout Inventory-Human Services Survey.

What is being tested

Self-Care and Burnout Prevention Program

Behavioral

Who is being recruted

Occupational Stress+4

+ Burnout, Psychological

+ Behavior

Over 18 Years

+3 Eligibility Criteria

See all eligibility criteria

How is the trial designed

Prevention Study

Interventional

Study Start: March 2026

See protocol details

Summary

Principal SponsorFundacion Arturo Lopez Perez

Study ContactNicole M Caire, Medical OncologistMore contacts

Last updated: March 12, 2026

Sourced from a government-validated database.Claim as a partner

Study start date: March 2, 2026

Actual date on which the first participant was enrolled.

This study focuses on first-year medical oncology residents affiliated with FALP. The main goal is to understand and prevent burnout among these residents over a period of 12 months. The study uses a mix of methods, including a self-care and burnout prevention program. This research is important as it aims to help future medical oncology residents manage stress and prevent burnout, improving their overall well-being and the quality of care they provide. During the study, participants will engage in a burnout prevention program that lasts 12 months. Their participation and attendance will be tracked throughout the program. The program's effectiveness will be measured using the Maslach Burnout Inventory-Human Services Survey (MBI-HSS), which looks at emotional exhaustion, depersonalization, and personal accomplishment. At the end of the program, residents will share their satisfaction and perceived usefulness of the program. Feedback from participants and faculty will be used to identify any challenges and opportunities for improvement in future programs.

Official TitleA Prospective Mixed-Methods Quasi-Experimental Study Evaluating Burnout Variation Over 12 Months and the Influence of a Self-Care and Burnout Prevention Program in First-Year Medical Oncology Residents

NCT07459868

Principal SponsorFundacion Arturo Lopez Perez

Study ContactNicole M Caire, Medical OncologistMore contacts

Last updated: March 12, 2026

Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

9 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.

Conditions

Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Occupational StressBurnout, PsychologicalBehaviorBehavioral SymptomsBurnout, ProfessionalOccupational DiseasesStress, Psychological

Criteria

1 inclusion criteria required to participate

First-year medical oncology residents at FALP; continued residency enrollment; minimum attendance requirement per protocol ( >= 75%)

2 exclusion criteria prevent from participating

Maternity leave during the study period

Interruption/withdrawal from the residency program

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.

Treatment Groups

Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group

Treatment Groups

Group I

Experimental

First-year medical oncology residents participate in a structured wellness program delivered over 12 months. Attendance is tracked, and feedback is collected to evaluate satisfaction and implementation.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has no location dataSave this study to your profile to know when the location data is available.

Recruiting soonNo study centers