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Behavioral Intervention

Mindfulness Training for Burnout (IMPACT Trial)

N/A
Waitlist Available
Led By Lee Wilke, MD, FACS
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (pre-intervention), post-intervention (3 months), follow up (6 months)
Awards & highlights

Summary

This trial aims to see if training healthcare professionals in mindfulness can help improve their well-being and teamwork when caring for cancer patients. They will enroll various healthcare professionals in oncology teams and study them for about

Who is the study for?
This trial is for healthcare professionals like nurses, medical assistants, social workers, technicians, and doctors working in oncology teams at UW Madison. They must be involved in direct patient care or support services to join.
What is being tested?
The study tests a mindfulness team training program called RENEW aimed at improving well-being and teamwork among oncology care providers. Participants will engage with the program over a period of up to 6 months.
What are the potential side effects?
Since this trial involves mindfulness practices rather than medication, there are no typical drug side effects; however, participants may experience emotional discomfort as they reflect on stressful work experiences.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (pre-intervention), post-intervention (3 months), follow up (6 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline (pre-intervention), post-intervention (3 months), follow up (6 months) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Acceptability of Intervention Measure (AIM)
Change in Teamwork Measure
Feasibility of Intervention Measure (FIM)
+2 more
Secondary study objectives
Change in Burnout measured by Maslach Burnout Inventory
Change in Resilience measured by Connor Davidson Resilience Scale (CD-RISC 2)
Change in Stress measured by Perceived Stress Scale (PSS)
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Mindfulness-Based Team Resilience TrainingExperimental Treatment1 Intervention

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Who is running the clinical trial?

University of Wisconsin, MadisonLead Sponsor
1,210 Previous Clinical Trials
3,157,689 Total Patients Enrolled
Lee Wilke, MD, FACSPrincipal InvestigatorUW Carbone Cancer Center
~33 spots leftby Aug 2025
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