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Clinical Trials/NCT06423183
NCT06423183
Completed
N/A

Interprofessional Mindfulness Practices Advancing Cancer Teamwork (IMPACT Study)

University of Wisconsin, Madison1 site in 1 country21 target enrollmentSeptember 26, 2024
ConditionsBurn Out

Overview

Phase
N/A
Intervention
Not specified
Conditions
Burn Out
Sponsor
University of Wisconsin, Madison
Enrollment
21
Locations
1
Primary Endpoint
Number of Participants Who Attend Each Session
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 26, 2024
End Date
December 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Number of Participants Who Attend Each Session

Time Frame: up to 3 months

Session 1 baseline, session 2 at 1 month, session 3 at 2 months, session 4 at 3 months

Acceptability of Intervention Measure (AIM)

Time Frame: up to 3 months

AIM 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.

Feasibility of Intervention Measure (FIM)

Time Frame: up to 3 months

FIM 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 Measure

Time Frame: baseline (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

Intervention Appropriateness Measure (IAM)

Time Frame: up to 3 months

IAM 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 Outcomes

  • Change in Stress measured by Perceived Stress Scale (PSS)(baseline (pre-intervention), post-intervention (3 months), follow up (6 months))
  • Change in Resilience measured by Connor Davidson Resilience Scale (CD-RISC 2)(baseline (pre-intervention), post-intervention (3 months), follow up (6 months))
  • Change in Well-being measured by Flourishing Index(baseline (pre-intervention), post-intervention (3 months), follow up (6 months))
  • Change in Burnout measured by Maslach Burnout Inventory(baseline (pre-intervention), post-intervention (3 months), follow up (6 months))

Study Sites (1)

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