42 Participants NeededMy employer runs this trial

Digital Mindfulness for Physician Burnout

(CALM-PR Trial)

GO
JT
Overseen ByJason T Tsichlis, MD, MS
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Northwestern University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores how different formats of a digital mindfulness program might help pediatric residents manage stress from their demanding medical training. Participants will use an online program called the Wakeful Digital Mindfulness Program, either selecting the length of their course or having it assigned. Researchers aim to determine if having a choice affects participants' engagement and completion rates. The trial is open to pediatric residents at Northwestern University who are willing to participate. As an unphased trial, this study offers a unique opportunity for residents to enhance their stress management skills and contribute to research that could benefit future medical professionals.

Do I have to stop taking my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It seems unlikely that you would need to stop, as the study focuses on a mindfulness program rather than a medical treatment.

What prior data suggests that the Wakeful Digital Mindfulness Program is safe for pediatric residents?

Research has shown that digital mindfulness programs like Wakeful are generally safe for participants. Many studies have found positive results, such as reduced burnout and improved mood among healthcare workers. Specifically, mindfulness practice can decrease emotional exhaustion and enhance stress management.

No specific safety issues have been reported with the Wakeful program. These programs typically involve guided meditation and are considered low-risk. Participants often find them manageable. The absence of serious side effects in similar programs suggests that Wakeful is likely safe for those considering joining the trial.12345

Why are researchers excited about this trial?

Researchers are excited about the Wakeful Digital Mindfulness Program because it offers a flexible approach to combating physician burnout, which is different from traditional methods like therapy or medication. Unlike conventional treatments, this program allows participants to choose the duration of their mindfulness training, potentially increasing engagement and effectiveness. Additionally, the digital format makes it accessible and convenient, fitting easily into busy schedules, which is crucial in a high-demand profession like healthcare.

What evidence suggests that the Wakeful Digital Mindfulness Program is effective for physician burnout?

Research has shown that digital mindfulness programs can help reduce burnout, especially in healthcare workers. One study found that a mindfulness program reduced burnout in healthcare professionals by 27%. Another study discovered that digital meditation greatly improved feelings of emotional exhaustion and cynicism, which are major components of burnout. Practicing mindfulness also boosts mood, stress management, and energy levels. This trial will evaluate the Wakeful Digital Mindfulness Program, with participants either choosing their program duration or being assigned one, to assess its effectiveness in lessening burnout symptoms in pediatric residents.24567

Are You a Good Fit for This Trial?

This trial is for current pediatric residents at Northwestern University, including those planning to continue in pediatrics. Participants must be willing and able to give informed consent. There are no other exclusions.

Inclusion Criteria

Willing and able to provide informed consent
Current categorical pediatrics residents at Northwestern University
Preliminary pediatrics residents who intend to continue in pediatrics

Exclusion Criteria

I am a pediatric resident who meets the study's basic requirements.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants engage in the Wakeful digital mindfulness program, choosing or being assigned a duration of 3, 5, or 7 weeks

3-7 weeks
Remote participation via digital platform

Follow-up

Participants complete post-intervention surveys and optional in-person debrief interviews to assess engagement and perceptions

2-4 weeks
1 optional in-person visit for debrief interview

What Are the Treatments Tested in This Trial?

Interventions

  • Wakeful Digital Mindfulness Program

Trial Overview

The study tests a flexible online mindfulness program called Wakeful. Residents are randomly assigned either to choose their course length (3, 5, or 7 weeks) or have it assigned. The goal is to see if having a choice improves engagement and satisfaction.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: No ChoiceExperimental Treatment1 Intervention
Group II: ChoiceExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Northwestern University

Lead Sponsor

Trials
1,674
Recruited
989,000+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/39854701/

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