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Interprofessional Mindfulness Practices Advancing Cancer Teamwork

Interprofessional Mindfulness Practices Advancing Cancer Teamwork (IMPACT Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06423183
Acronym
IMPACT
Enrollment
21
Registered
2024-05-21
Start date
2024-09-26
Completion date
2024-12-31
Last updated
2025-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn Out

Keywords

oncology, health care, clinicians, mindfulness, well-being

Brief summary

The purpose of the research is to understand if mindfulness team training can improve the well-being and teamwork in caring for oncology patients. This study will enroll healthcare professionals in oncology teams, including clinic nurses, nurse managers, medical assistants, social workers, technicians, patient navigators, advanced practice providers, and physicians at UW Madison. Participants will be on study for up to approximately 6 months.

Detailed description

Aim 1: Determine the effect of resilience training on team resilience and well-being. The investigators test the hypothesis that resilience training provided to interprofessional oncology care teams will improve team resilience and individual well-being. Aim 2: Determine the feasibility and acceptability of a resilience training on team resilience. The investigators test the hypothesis that resilience training is feasible and acceptable in interprofessional oncology care teams.

Interventions

BEHAVIORALA Mindful Approach to Building a Resilient Healthcare Workforce (RENEW)

Synchronous, 4-month intervention that teaches skills in mindfulness, stress management, and resilience as an individual and as a team. Sessions occur monthly and include a 1 hour in-person introductory session followed by 3 50-minute virtual sessions.

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This study is a prospective, pre-post study at a single institution

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* A care provider in an oncology clinic team (clinic nurse, nurse manager, medical assistant, technician, social worker, patient navigator, advanced practice provider, physician)

Exclusion criteria

* Does not participate in patient care or support services

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of Intervention Measure (FIM)up to 3 monthsFIM is a 4-item survey scored on a 5 point likert scale from 1 (completely disagree) to 5 (completely agree), where higher scores indicate greater feasibility.
Change in Teamwork Measurebaseline (pre-intervention), post-intervention (3 months), follow up (6 months)4-item Edmondson's psychology safety scale is scored on a likert scale from 1 (strongly disagree) to 7 (strongly agree), where higher scores indicate higher psychology safety
Number of Participants Who Attend Each Sessionup to 3 monthsSession 1 baseline, session 2 at 1 month, session 3 at 2 months, session 4 at 3 months
Acceptability of Intervention Measure (AIM)up to 3 monthsAIM is a 4-item survey scored on a 5 point likert scale from 1 (completely disagree) to 5 (completely agree), where higher scores indicate greater acceptability.
Intervention Appropriateness Measure (IAM)up to 3 monthsIAM is a 4-item survey scored on a 5 point likert scale from 1 (completely disagree) to 5 (completely agree), where higher scores indicate greater appropriateness.

Secondary

MeasureTime frameDescription
Change in Burnout measured by Maslach Burnout Inventorybaseline (pre-intervention), post-intervention (3 months), follow up (6 months)This is a 2-item survey scored from 0-6 where higher scores indicate increased burnout.
Change in Resilience measured by Connor Davidson Resilience Scale (CD-RISC 2)baseline (pre-intervention), post-intervention (3 months), follow up (6 months)CD-RISC 2 is a 2-item survey each scored on a 5 point likert scale from 0 (not true at all) to 4 (true nearly all of the time), higher scores indicate increased resilience.
Change in Well-being measured by Flourishing Indexbaseline (pre-intervention), post-intervention (3 months), follow up (6 months)Flourishing measure is a 12-item survey that measure well being in each of 6 domains: happiness and life satisfaction; mental and physical health; meaning and purpose; character and virtue; close social relationships; financial and material stability. Each domain is scored from 0 - 10 where higher numbers are indicative of increased well being.
Change in Stress measured by Perceived Stress Scale (PSS)baseline (pre-intervention), post-intervention (3 months), follow up (6 months)PSS is a 10-item survey scored from 0 (never) to 4 (very often) for a total possible range of scores from 0-40 where higher scores indicate higher perceived stress.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026