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Clinical Trials/NCT03403335
NCT03403335
Completed
Not Applicable

Mindfulness Practices for Healthcare Professional Trainees

Virginia Commonwealth University1 site in 1 country57 target enrollmentFebruary 9, 2018
ConditionsStress

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress
Sponsor
Virginia Commonwealth University
Enrollment
57
Locations
1
Primary Endpoint
Change in burnout
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

A newly developed intervention, Mindfulness Based Practices for Health Care Professionals in Training: Clinical Applications, will be piloted to determine the feasibility and accessibility within this population. The purpose of the proposed study is to assess the change in perceived stress at work/school and psychological symptomology; i.e., depression, stress, emotion regulation, and dispositional mindfulness, from pre to post intervention in health care professional students and when compared to a matched control group.

Detailed Description

The proposed study aims to investigate an 8-week intervention: Mindfulness Based Practices for Health Care Professionals in Training: Clinical Applications. During the intervention, participants will engage in didactic education, experiential mindfulness practices, including gentle yoga, and group dialogue. The aim of the study is to investigate the feasibility of this intervention in producing measurable differences between the participants and matched controls on their perception of their well-being and clinical work.

Registry
clinicaltrials.gov
Start Date
February 9, 2018
End Date
April 28, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Students/faculty from any health care department at VCU

Exclusion Criteria

  • Anyone who is not a student/faculty from a health care department at VCU

Outcomes

Primary Outcomes

Change in burnout

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using Maslach Burnout Inventory a 22 item screening tool with higher values indicating more burnout

Change in depressive symptoms

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using Patient Health Questionnaire 9. 9-items with lower values indicating less depression

Change in state anxiety

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using State Trait Anxiety Inventory -- a 20 item measure with some items reverse scored and higher scored indicating higher state anxiety

Change in ruminative thinking

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using Rumination Response Scale -- a 10 item measure with higher scores indicating higher rumination

Change in stress

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using Perceived Stress Scale -- a 14-item scale with higher scores indicating higher levels of stress

Change in dispositional mindfulness

Time Frame: administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up

Assessed using Five Facet Mindfulness Questionnaire -- a 39-item measure of 5 domains of mindfulness in daily life, with higher scores indicating higher levels of mindfulness

Change in cognitive functioning

Time Frame: administered at baseline and post-intervention (8 weeks)

Assessed using Trail Making Test A \& B -- a brief task requiring respondents to connect numbered dots and then switch between number and letters, speed and accuracy are both recorded

Secondary Outcomes

  • Change in interprofessional attitudes measure(administered at baseline, post-intervention (8 weeks), and 3 month post-intervention follow-up)
  • Follow-up Interview of Perceptions of Mindfulness and Interprofessional Education(assessed at 3-month post-intervention follow-up)

Study Sites (1)

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