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Interprofessional Group Intervention to Promote Faculty Wellbeing and Engagement

Primary Purpose

Burnout, Professional

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Discussion Guide
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Burnout, Professional

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Physican in the Department of Obstetrics and Gynecology at Massachusetts General Hospital
  • Nurse Practitioner in the Department of Obstetrics and Gynecology at Massachusetts General Hospital
  • Certified Nurse Midwife in the Department of Obstetrics and Gynecology at Massachusetts General Hospital

Exclusion Criteria:

  • None

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Providers were placed in small groups and given the intervention of a discussion guide to facilitate discussion.

Providers were placed in small groups and not given a discussion guide to facilitate discussion.

Outcomes

Primary Outcome Measures

Burnout
Change from baseline in 2 item Maslach Burnout Inventory scores before and after the intervention. Minimum score: 2; Maximum score: 14 Higher score = more burnt out (worse outcome)
Stress from Uncertainty
Change in scores on Physician Response to Uncertainty Scale before and after intervention Minimum score: 6; Maximum score: 90 Higher score = increased stress due to uncertainty (worse outcome)
Work Engagement
Change in scores on Utrecht Work Engagement Scale before and after intervention Minimum score: 0; Maximum score: 54 Higher score = higher engagement at work (better outcome)
Urine oxytocin
Change from baseline in the level of urine oxytocin before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Salivary Oxytocin
Change from baseline in the level of salivary oxytocin before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Salivary Cortisol
Change from baseline in the level of salivary cortisol before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Hair Cortisol
Change from baseline in hair cortisol levels. Maximum and minimum levels are not known and any change up or down is interesting.
Work Empowerment Scale
Minimum score: 12; Maximum score: 84 Change from baseline on Work Empowerment Scale before and after intervention. Higher score = higher empowerment at work (better outcome)

Secondary Outcome Measures

Full Information

First Posted
March 3, 2020
Last Updated
March 10, 2020
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04305886
Brief Title
Interprofessional Group Intervention to Promote Faculty Wellbeing and Engagement
Official Title
Interprofessional Group Intervention to Promote Faculty Wellbeing and Engagement
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
September 30, 2018 (Actual)
Study Completion Date
September 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A randomized trial of an interprofessional intervention to reduce burnout and enhance professional engagement in physicians, certified nurse midwives, and nurse practitioners.
Detailed Description
To test the hypothesis that an intervention involving self-facilitated interprofessional group meetings would result in improvement in wellbeing and to determine whether use of a written curriculum provided increased benefit, the following study is conducted: Practicing clinical faculty in the Department of Obstetrics and Gynecology at the Massachusetts General Hospital were recruited to participate in three monthly small groups over dinner. Participants were randomized to a control group, which met without any specified guidelines for discussion content, or to receive an intervention which consisted of a one-page discussion guide addressing themes relevant to challenges in the healthcare environment: reframing challenging patient interactions; embracing uncertainty in work; and coping with errors, near misses, and bad outcomes. Outcomes included burnout, empowerment and engagement in work, stress from uncertainty assessed using validated metrics, and perception of of collegiality and community. All participants were also offered the option of participating in evaluation of biomarkers. To test the hypothesis that an increased sense of bonding and relational connection, and reduced stress levels would be reflected by changes in hormone levels during the meeting and over the course of the study. Faculty who opted into this portion of the study gave the following samples: Urine Oxytocin before and after the first and third group meetings Salivary Oxytocin before and after the first and third group meetings Salivary Cortisol before and after the first and third group meetings Hair Cortisol at the beginning of the study and at the end of the study (a roughly three month interval). An optional focus group was conducted after the three monthly sessions. All participants signed a consent form prior to participating in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Professional

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Providers were placed in small groups and given the intervention of a discussion guide to facilitate discussion.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Providers were placed in small groups and not given a discussion guide to facilitate discussion.
Intervention Type
Other
Intervention Name(s)
Discussion Guide
Intervention Description
Written list of prompts to facilitate discussion
Primary Outcome Measure Information:
Title
Burnout
Description
Change from baseline in 2 item Maslach Burnout Inventory scores before and after the intervention. Minimum score: 2; Maximum score: 14 Higher score = more burnt out (worse outcome)
Time Frame
Change over the three month study period. Baseline measurement and immediately after final intervention.
Title
Stress from Uncertainty
Description
Change in scores on Physician Response to Uncertainty Scale before and after intervention Minimum score: 6; Maximum score: 90 Higher score = increased stress due to uncertainty (worse outcome)
Time Frame
Change over the three month study period. Baseline measurement and immediately after final intervention.
Title
Work Engagement
Description
Change in scores on Utrecht Work Engagement Scale before and after intervention Minimum score: 0; Maximum score: 54 Higher score = higher engagement at work (better outcome)
Time Frame
Change over the three month study period. Baseline measurement and immediately after final intervention.
Title
Urine oxytocin
Description
Change from baseline in the level of urine oxytocin before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Time Frame
Two samples were taken one hour apart at baseline, and this was repeated three months later.
Title
Salivary Oxytocin
Description
Change from baseline in the level of salivary oxytocin before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Time Frame
Two samples were taken one hour apart at baseline, and this was repeated three months later
Title
Salivary Cortisol
Description
Change from baseline in the level of salivary cortisol before and after each intervention. This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
Time Frame
Two samples were taken one hour apart at baseline, and this was repeated three months later
Title
Hair Cortisol
Description
Change from baseline in hair cortisol levels. Maximum and minimum levels are not known and any change up or down is interesting.
Time Frame
Change over the three month study period. Baseline measurement and immediately after final intervention.
Title
Work Empowerment Scale
Description
Minimum score: 12; Maximum score: 84 Change from baseline on Work Empowerment Scale before and after intervention. Higher score = higher empowerment at work (better outcome)
Time Frame
Change over the three month study period. Baseline measurement and immediately after final intervention.

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Physican in the Department of Obstetrics and Gynecology at Massachusetts General Hospital Nurse Practitioner in the Department of Obstetrics and Gynecology at Massachusetts General Hospital Certified Nurse Midwife in the Department of Obstetrics and Gynecology at Massachusetts General Hospital Exclusion Criteria: None
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Interprofessional Group Intervention to Promote Faculty Wellbeing and Engagement

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