A Pilot Study of RISE for Nurse Managers

February 25, 2022 updated by: AdventHealth

A Pilot Study of RISE (Resilience, Insight, Self-Compassion, Empowerment) for Nurse Managers

The purpose of this study is to determine whether RISE for Nurse Managers has a significant impact on nurse managers' post-traumatic growth, resilience, insight, self-compassion, and empowerment, as well as mental well-being, in their personal lives and their working environment.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Orlando, Florida, United States, 32804
        • AdventHealth Orlando

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Adult ≥ 18 years old
  2. Licensed as an RN
  3. Nurse manager employed by AdventHealth in a hospital-based setting at the Altamonte Springs, Apopka, Carrollwood, Celebration, Connerton, Dade City, Daytona Beach, DeLand, East Orlando, Fish Memorial, Heart of Florida, Kissimmee, Lake Placid, Lake Wales, New Smyrna Beach, North Pinellas, Ocala, Orlando, Palm Coast, Sebring, Tampa, Waterman, Wauchula, Wesley Chapel, Winter Garden, Winter Park, or Zephyrhills campus
  4. Able to speak, read, and understand English fluently
  5. Able to provide informed consent
  6. Willing and able to comply with all study procedures and requirements for the duration of the study

Exclusion Criteria:

1. Employed as a direct care nurse or in another level of nursing leadership (i.e., assistant nurse manager, director of nursing, executive leader)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Counseling and Surveys
nine 90-minute weekly psychoeducational group sessions facilitated by a licensed mental health counselor (LMHC).
nine 90-minute weekly psychoeducational group sessions facilitated by a licensed mental health counselor (LMHC).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Posttraumatic Growth Inventory
Time Frame: Change from Baseline to 6 months
21 item questionnaire with a scale of 0-5, with 0 meaning I did not experience this change as a result of my crisis to 5 meaning I experienced this change to a very great degree as a result of my crisis
Change from Baseline to 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Brief Cope
Time Frame: Change from Baseline to 6 months
28 item questionnaire with a scale of 1-4, with 1 meaning I haven't been doing this at all; and 4 meaning I've been doing this a lot
Change from Baseline to 6 months
Brief Index of Affective Job Satisfaction
Time Frame: Change from Baseline to 6 months
4 item questionnaire with a scale of 1-5, with 1 meaning strongly disagree; and 5 meaning strongly agree
Change from Baseline to 6 months
Brief Resilience Scale
Time Frame: Change from Baseline to 6 months
6 item questionnaire with a scale of 1-5, with 1 meaning strongly disagree; and 5 meaning strongly agree
Change from Baseline to 6 months
Psychological Empowerment Instrument
Time Frame: Change from Baseline to 6 months
12 item questionnaire with a scale of A-G, with A meaning very strongly disagree; and G meaning very strongly agree
Change from Baseline to 6 months
Perceived Stress Scale
Time Frame: Change from Baseline to 6 months
10 item questionnaire with a scale of 0-4, with 0 meaning never; and 4 meaning very often
Change from Baseline to 6 months
Maslach Burnout Inventory General Survey
Time Frame: Change from Baseline to 6 months
16 item questionnaire with a scale of 0-6 with 0 meaning never; and 6 meaning everyday
Change from Baseline to 6 months
Self-Compassion Scale - Short Form
Time Frame: Change from Baseline to 6 months
12 item questionnaire with a scale of 1-5, with 1 meaning almost never; and 5 meaning almost always
Change from Baseline to 6 months
Self-Reflection and Insight Scale
Time Frame: Change from Baseline to 6 months
20 item questionnaire with a scale of 1-6; with 1 meaning strongly disagree; and 6 meaning strongly agree
Change from Baseline to 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 13, 2021

Primary Completion (Actual)

December 31, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

March 3, 2020

First Submitted That Met QC Criteria

July 28, 2021

First Posted (Actual)

August 3, 2021

Study Record Updates

Last Update Posted (Actual)

February 28, 2022

Last Update Submitted That Met QC Criteria

February 25, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 1504917

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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