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Coaching for Advanced Practice Providers

Primary Purpose

Burnout, Professional

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
hybrid asynchronous-synchronous group coaching program
treatment as usual group (TAU)
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Burnout, Professional focused on measuring Advanced Practice Providers, APPs, Coaching, Healthcare provider, Nurse burnout, Wellness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Advanced Practice Providers (nurse practitioners, physician assistants, certified midwife nurses, certified registered nurse anesthetists, anesthesiology assistants, and clinical nurse specialists) at Children's Healthcare of Atlanta, Emory University, and CU and its affiliate hospitals. Pregnant women will be included in this population, though this inclusion is incidental. Exclusion Criteria: adults unable to consent, individuals who are not adults, prisoners, cognitively impaired or individuals with impaired decision-making capacity and individuals who do not clearly understand English.

Sites / Locations

  • University of ColoradoRecruiting
  • Children's Healthcare of AtlantaRecruiting
  • Emory Healthcare SystemRecruiting
  • Emory UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Group Coaching Program

Usual Treatment

Arm Description

The study intervention is a hybrid asynchronous-synchronous group coaching treatment that will occur over four months. Participants will be given access to a members-only, web-based platform to access the intervention.

This group will participate in the study intervention following a 4-month waitlist/control group.

Outcomes

Primary Outcome Measures

Change in Burnout
Burnout as defined by the Maslach Burnout Inventory (MBI). The Maslach burnout inventory (MBI) is a 22-item measurement of worker burnout that assesses emotional exhaustion (EE), depersonalization (DP), and personal fulfillment (PF) domains. Possible scores range from 0-6 on a Likert scale for each item. Scores of EE ≥ 27 points, DP ≥ 10, and PF <33 would indicate a high degree of burnout. Scores of EE≤18 points, DP≤5 points, and PF≥40 points would indicate a low degree of burnout.
Change in the percentage of participants that accept the program course
Data collection will be at baseline, month 4, and month 9 for both groups.
Percentage of participants who watch program calls
Number of participants who watch program calls. Data collection will only be at the end of participation Group Coaching Program.
Change in the percentage of participants that complete >50% of self-study worksheets
Number of participants who complete >50% of self-study worksheets. Data collection will only be at the end of participation Group Coaching Program.
Change in the percentage of participants that use the Ask A Coach Forum at least once
Percentage of participants that use the Ask A Coach Forum at least once. Data collection will only be at the end of participation Group Coaching Program.
Change in the rate of participation in the program
Percentage of participants that complete the outcome measures (pre/post surveys). Data collection will be at month 4 and month 9 for both groups.

Secondary Outcome Measures

Change in Trauma Symptoms of Discrimination Scale
This two-part scale measures the experiences of discrimination using trauma symptoms. Part 1 includes 21 questions where the participant can respond to agree or disagree with the statement using Likert scale response options. Part 2 of the scale allows the respondent to allocate what percentage of their identity they experience discrimination on (i.e. race/ethnicity: 70%, disability: 20 %, and gender: 10%).
Change in Self-Compassion
Self-Compassion as defined by Neff's Self Compassion Score Short Form is a 12-item measurement of self-compassion. Possible scores range from 0-6 on a Likert scale for each item, where the higher scale scores indicate greater self-compassion. Scores of 1.0- 2.49 are considered to be low, between 2.5-3.5 to be moderate, and 3.51-5.0 to be high.
Change in Moral Injury
Moral Injury as defined by the Moral Injury Symptom Scale for Health Professions. (MISS-HP) is a 10-item measurement of moral injury. Possible scores range from 0-5 on a Likert scale for each item, where the higher scale scores indicate greater moral injury. Scores >35 (on a possible score range of 10 to 100) are considered high for moral injury symptoms causing moderate to extreme problems with family, social, and occupational functioning.
Change in the Young's Imposter Syndrome Symptoms Scale
Imposter Syndrome as defined by Young's Imposter Syndrome Symptoms Scale. (YISS) is an 8-item measurement of imposter syndrome. Scoring is yes/no where a score of >5/8 is felt to be positive for imposter syndrome.
Change in the intention to leave
Intent-to-leave is defined by a single-item question, on a 3-point Likert scale, where the higher the score reflects more intention to leave the current position. Followed by a single multiple-choice question as to why the participant is leaving.
Change in Loneliness
Loneliness as defined by the University of California, Los Angeles (UCLA) 3-item Loneliness Scale. It is a 3-item measure of relational connectedness, social connectedness, and self-perceived isolation. Items are measured on a 3-point scale where a score range of 3-5 is "not lonely" and a score range of 6-9 is "lonely".
Change in Self Reflection and Insight Scale
Self-reflection and insight as defined by Self Reflection and Insight Short Scale (SIRSS). It is a 12-point item measurement of the capacity to reflect on oneself and to think about one's thoughts, experiences, and actions on a 7-point Likert scale, where higher scores reflect more inspection, evaluation and perception of thoughts, beliefs, feelings, and behaviors.

Full Information

First Posted
June 8, 2023
Last Updated
August 21, 2023
Sponsor
Emory University
Collaborators
Children's Healthcare of Atlanta, University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT05938556
Brief Title
Coaching for Advanced Practice Providers
Official Title
The Impact of a Multicenter Randomized Control Trial of Hybrid Synchronous-Asynchronous Virtual Group Coaching on Burnout and Retention in Advanced Practice Providers
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 14, 2023 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Children's Healthcare of Atlanta, University of Colorado, Denver

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
This study aims to determine if online coaching is feasible in advanced practice providers (APP) and can impact burnout. The study will recruit APPs from Children's Healthcare of Atlanta (CHOA), Emory, Colorado University (CU), and their affiliate hospitals through online consent sent via email. Interventions will include online video coaching, written coaching, and self-coaching through self-study material.
Detailed Description
The purpose of this study is to determine the feasibility of establishing a coaching program directed toward Advanced Practice Providers (APPs), to determine the generalizability of tools shown to relieve physician burnout in the population of APPs, and to advance research in the field of healthcare wellness. The coaching group will have a curriculum of self-study modules, pre-recorded webinars, and worksheets. The coaching group will also have access to two live group calls per week as well as an online forum to receive anonymously written coaching. After four months, participants will be switched to the other group, so that each participant is exposed to treatment but at separate times. At the completion of each intervention time point, participants will fill out a post-study survey.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Professional
Keywords
Advanced Practice Providers, APPs, Coaching, Healthcare provider, Nurse burnout, Wellness

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will be randomly assigned to receive either four months of group coaching or treatment as usual. After fourth months of the assigned treatment, the two arms will switch for another four months of either group coaching or treatment as usual.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group Coaching Program
Arm Type
Experimental
Arm Description
The study intervention is a hybrid asynchronous-synchronous group coaching treatment that will occur over four months. Participants will be given access to a members-only, web-based platform to access the intervention.
Arm Title
Usual Treatment
Arm Type
Placebo Comparator
Arm Description
This group will participate in the study intervention following a 4-month waitlist/control group.
Intervention Type
Behavioral
Intervention Name(s)
hybrid asynchronous-synchronous group coaching program
Other Intervention Name(s)
group coaching program
Intervention Description
A hybrid asynchronous-synchronous program. The synchronous part has two weekly recorded live group coaching calls for four months. The asynchronous consist of 1) on-demand replies to recorded coaching calls, 2) Self-coaching through weekly self-study modules and worksheets, and 3) written Ask A Coach. Content modified per needs of APPs by a physician, a certified coach, and an APP who is also a Co-I. The curriculum has weekly themes that build. Month-1 consists of 1) Introduction to the Model, 2) How to Feel Better, 3) Defining Your Purpose, and 4) Living Your Purpose. Month-2 consists of 1) Growth Mindset, 2) Welcoming Feedback and Assessment Bias, 3) Feeling Valued and Belonging, and 4) How to Deal with Hidden Expectations. Month-3 consists of 1) Imposter Syndrome, 2) Perfectionism, 3) Approval Addiction, and 4) How to Change Your Thoughts. Month-4 consists of 1) How to deal with Ambiguity, 2) Confidence, 3) Self-Appreciation and Self-Compassion, and 4) Celebrate the New You.
Intervention Type
Other
Intervention Name(s)
treatment as usual group (TAU)
Other Intervention Name(s)
TAU
Intervention Description
The treatment as usual group will consist of any structural or programmatic interventions, resources, lectures, curriculum, etc. offered at the participants' hospital of employment. Thus, this active control is designed to represent a best-case alternative to group coaching, making it a more rigorous form of control. Participants randomly assigned to TAU will also continue any structural or programmatic interventions or resources they were previously participating in.
Primary Outcome Measure Information:
Title
Change in Burnout
Description
Burnout as defined by the Maslach Burnout Inventory (MBI). The Maslach burnout inventory (MBI) is a 22-item measurement of worker burnout that assesses emotional exhaustion (EE), depersonalization (DP), and personal fulfillment (PF) domains. Possible scores range from 0-6 on a Likert scale for each item. Scores of EE ≥ 27 points, DP ≥ 10, and PF <33 would indicate a high degree of burnout. Scores of EE≤18 points, DP≤5 points, and PF≥40 points would indicate a low degree of burnout.
Time Frame
Baseline, 4 months, 9 months
Title
Change in the percentage of participants that accept the program course
Description
Data collection will be at baseline, month 4, and month 9 for both groups.
Time Frame
Baseline, 4 months, 9 months
Title
Percentage of participants who watch program calls
Description
Number of participants who watch program calls. Data collection will only be at the end of participation Group Coaching Program.
Time Frame
4 month or 9 months
Title
Change in the percentage of participants that complete >50% of self-study worksheets
Description
Number of participants who complete >50% of self-study worksheets. Data collection will only be at the end of participation Group Coaching Program.
Time Frame
4 month or 9 months
Title
Change in the percentage of participants that use the Ask A Coach Forum at least once
Description
Percentage of participants that use the Ask A Coach Forum at least once. Data collection will only be at the end of participation Group Coaching Program.
Time Frame
4 month or 9 months
Title
Change in the rate of participation in the program
Description
Percentage of participants that complete the outcome measures (pre/post surveys). Data collection will be at month 4 and month 9 for both groups.
Time Frame
Baseline, 4 months, 9 months
Secondary Outcome Measure Information:
Title
Change in Trauma Symptoms of Discrimination Scale
Description
This two-part scale measures the experiences of discrimination using trauma symptoms. Part 1 includes 21 questions where the participant can respond to agree or disagree with the statement using Likert scale response options. Part 2 of the scale allows the respondent to allocate what percentage of their identity they experience discrimination on (i.e. race/ethnicity: 70%, disability: 20 %, and gender: 10%).
Time Frame
Baseline, 4 months, 9 months
Title
Change in Self-Compassion
Description
Self-Compassion as defined by Neff's Self Compassion Score Short Form is a 12-item measurement of self-compassion. Possible scores range from 0-6 on a Likert scale for each item, where the higher scale scores indicate greater self-compassion. Scores of 1.0- 2.49 are considered to be low, between 2.5-3.5 to be moderate, and 3.51-5.0 to be high.
Time Frame
Baseline, 4 months, 9 months
Title
Change in Moral Injury
Description
Moral Injury as defined by the Moral Injury Symptom Scale for Health Professions. (MISS-HP) is a 10-item measurement of moral injury. Possible scores range from 0-5 on a Likert scale for each item, where the higher scale scores indicate greater moral injury. Scores >35 (on a possible score range of 10 to 100) are considered high for moral injury symptoms causing moderate to extreme problems with family, social, and occupational functioning.
Time Frame
Baseline, 4 months, 9 months
Title
Change in the Young's Imposter Syndrome Symptoms Scale
Description
Imposter Syndrome as defined by Young's Imposter Syndrome Symptoms Scale. (YISS) is an 8-item measurement of imposter syndrome. Scoring is yes/no where a score of >5/8 is felt to be positive for imposter syndrome.
Time Frame
Baseline, 4 months, 9 months
Title
Change in the intention to leave
Description
Intent-to-leave is defined by a single-item question, on a 3-point Likert scale, where the higher the score reflects more intention to leave the current position. Followed by a single multiple-choice question as to why the participant is leaving.
Time Frame
Baseline, 4 months, 9 months
Title
Change in Loneliness
Description
Loneliness as defined by the University of California, Los Angeles (UCLA) 3-item Loneliness Scale. It is a 3-item measure of relational connectedness, social connectedness, and self-perceived isolation. Items are measured on a 3-point scale where a score range of 3-5 is "not lonely" and a score range of 6-9 is "lonely".
Time Frame
Baseline, 4 months, 9 months
Title
Change in Self Reflection and Insight Scale
Description
Self-reflection and insight as defined by Self Reflection and Insight Short Scale (SIRSS). It is a 12-point item measurement of the capacity to reflect on oneself and to think about one's thoughts, experiences, and actions on a 7-point Likert scale, where higher scores reflect more inspection, evaluation and perception of thoughts, beliefs, feelings, and behaviors.
Time Frame
Baseline, 4 months, 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Advanced Practice Providers (nurse practitioners, physician assistants, certified midwife nurses, certified registered nurse anesthetists, anesthesiology assistants, and clinical nurse specialists) at Children's Healthcare of Atlanta, Emory University, and CU and its affiliate hospitals. Pregnant women will be included in this population, though this inclusion is incidental. Exclusion Criteria: adults unable to consent, individuals who are not adults, prisoners, cognitively impaired or individuals with impaired decision-making capacity and individuals who do not clearly understand English.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zahidee (Saidie) Rodriguez, MD
Phone
678-469-6859
Email
rodriguezz@kidsheart.com
First Name & Middle Initial & Last Name or Official Title & Degree
Brooke Seitter
Phone
404-785-6953
Email
Brooke.Seitter@choa.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zahidee (Saidie) Rodriguez, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Colorado
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Individual Site Status
Recruiting
Facility Name
Children's Healthcare of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zahidee (Saidie) Rodriguez, MD
Facility Name
Emory Healthcare System
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30329
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Investigators will share all of the individual participant data collected during the trial, after deidentification.
IPD Sharing Time Frame
Beginning 3 months and ending 5 years following article publication.
IPD Sharing Access Criteria
Proposals should be directed to rodriguezz@kidsheart.com with a signed data access agreement, for up to 5 yrs (example 2 language)

Learn more about this trial

Coaching for Advanced Practice Providers

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