Stress Clinical Trial
— RISEOfficial title:
A Randomized Controlled Trial of RISE for Nurse Leaders
NCT number | NCT05254600 |
Other study ID # | 1839775 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 28, 2022 |
Est. completion date | May 15, 2023 |
Verified date | June 2023 |
Source | AdventHealth |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine whether RISE for Nurse Leaders has a significant impact on nurse leaders' post-traumatic growth, resilience, insight, self-compassion, and empowerment, as well as mental well-being, in their personal lives and their working environment.
Status | Completed |
Enrollment | 80 |
Est. completion date | May 15, 2023 |
Est. primary completion date | March 15, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult = 18 years old - Licensed as an RN - Unit-based nurse leader (i.e., assistant nurse manager, nurse manager) employed by AdventHealth in a hospital-based setting at the Altamonte Springs, Apopka, Celebration, Daytona Beach, DeLand, East Orlando, Fish Memorial, Kissimmee, New Smyrna Beach, Orlando, Palm Coast, Waterman, or Winter Park campus - Able to speak, read, and understand English fluently - Able to provide informed consent - Willing and able to comply with all study procedures and requirements for the duration of the study. Exclusion Criteria: - Employed as a direct care nurse or in another level of nursing leadership (i.e., director of nursing, executive leader) - A study participant of IRBNet #1504917 titled A Pilot Study of RISE for Nurse Managers |
Country | Name | City | State |
---|---|---|---|
United States | AdventHealth Orlando | Orlando | Florida |
Lead Sponsor | Collaborator |
---|---|
AdventHealth |
United States,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Posttraumatic Growth Inventory | 21 item questionnaire with a scale of 0-5, with 0 meaning I did not experience this change as a result of my crisis; and 5 meaning I experienced this change to a very great degree as a result of my crisis | Group comparison from baseline to 3-month follow-up | |
Secondary | Brief Index of Affective Job Satisfaction | 4 item questionnaire with a scale of 1-5, with 1 meaning strongly disagree; and 5 meaning strongly agree | Group comparison from baseline to 3-month follow-up | |
Secondary | Brief Resilience Scale | 6 item questionnaire with a scale of 1-5, with 1 meaning strongly disagree; and 5 meaning strongly agree | Group comparison from baseline to 3-month follow-up | |
Secondary | General Self-Efficacy Scale | 10 item questionnaire with a scale of 1-4, with 1 meaning not at all true; and 4 meaning exactly true | Group comparison from baseline to 3-month follow-up | |
Secondary | Perceived Stress Scale | 10 item questionnaire with a scale of 0-4, with 0 meaning never; and 4 meaning very often | Group comparison from baseline to 3-month follow-up | |
Secondary | Professional Quality of Life (ProQOL) Scale | 30 item questionnaire with a scale of 1-5 with 1 meaning never; and 5 meaning very often | Group comparison from baseline to 3-month follow-up | |
Secondary | Psychological Empowerment Instrument | 12 item questionnaire with a scale of A-G, with A meaning very strongly disagree; and G meaning very strongly agree | Group comparison from baseline to 3-month follow-up | |
Secondary | Self-Reflection and Insight Scale | 20 item questionnaire with a scale of 1-6; with 1 meaning strongly disagree; and 6 meaning strongly agree | Group comparison from baseline to 3-month follow-up |
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