Coaching for Advanced Practice Providers

Sponsor
Emory University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05938556
Collaborator
Children's Healthcare of Atlanta (Other), University of Colorado, Denver (Other)
300
4
2
11
75
6.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: hybrid asynchronous-synchronous group coaching program
  • Other: treatment as usual group
N/A

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 different times. At the completion of each intervention time point, participants will fill out a post-study survey.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Intervention 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.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)
Primary Purpose:
Prevention
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
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group Coaching Program

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.

Behavioral: hybrid asynchronous-synchronous group coaching program
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.
Other Names:
  • group coaching program
  • Placebo Comparator: Usual Treatment

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

    Other: treatment as usual group
    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.
    Other Names:
  • TAU
  • Outcome Measures

    Primary Outcome Measures

    1. Change in the rate of participation in the program [4 months and 9 months]

      Percentage of participants that complete the outcome measures (pre/post surveys). Data collection will be at month 4 for the intervention group and month 9 for both groups.

    2. Change in Burnout [Baseline, 4 months and 9 months]

      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.

    Secondary Outcome Measures

    1. Change in Trauma Symptoms of Discrimination Scale [Baseline, 4 months and 9 months]

      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%).

    2. Change in Self-Compassion [Baseline, 4 months and 9 months]

      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.

    3. Change in Moral Injury [Baseline, 4 months and 9 months]

      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.

    4. Change in the Young's Imposter Syndrome Symptoms Scale [Baseline, 4 months and 9 months]

      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.

    5. Change in the intention to leave [Baseline, 4 months and 9 months]

      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.

    6. Change in Loneliness [Baseline, 4 months and 9 months]

      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".

    7. Change in Self Reflection and Insight Scale [Baseline, 4 months and 9 months]

      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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Advanced Practice Providers (nurse practitioners, physician assistants, clinical nurse specialists, and certified registered nurse anesthetists) 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Colorado Denver Colorado United States 80220
    2 Children's Healthcare of Atlanta Atlanta Georgia United States 30322
    3 Emory Healthcare System Atlanta Georgia United States 30322
    4 Emory University Atlanta Georgia United States 30329

    Sponsors and Collaborators

    • Emory University
    • Children's Healthcare of Atlanta
    • University of Colorado, Denver

    Investigators

    • Principal Investigator: Zahidee (Saidie) Rodriguez, MD, Emory University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Zahidee (Saidie) Rodriguez, Assistant Professor, Emory University
    ClinicalTrials.gov Identifier:
    NCT05938556
    Other Study ID Numbers:
    • STUDY00005675
    First Posted:
    Jul 10, 2023
    Last Update Posted:
    Jul 10, 2023
    Last Verified:
    Jul 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Zahidee (Saidie) Rodriguez, Assistant Professor, Emory University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 10, 2023