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Achieving Resilience in Acute Care Nurses (ARISE).

Primary Purpose

Stress, Psychological, Compassion Fatigue

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
ARISE
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stress, Psychological focused on measuring Resilience, Workplace Stress, Occupational Fatigue, Compassion Fatigue, Peer Support, Self-Care, Employee Assistance

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Nurse in the medical-surgical and trauma-neurosurgical intensive care units (MSICU and TNICU) and the medical/surgical floor (9CCN),
  • full-time or part-time employment status,
  • approval of clinical leader manager (CLM),
  • receipt of written informed consent.

Exclusion Crieria:

  • casual employment status
  • inability to attend intervention days

Sites / Locations

  • St. Michael's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

ARISE Intervention

Control Group

Arm Description

Nurses who participate in the 1.5 day ARISE Intervention

Nurses who do not participate in the ARISE Intervention

Outcomes

Primary Outcome Measures

Connor Davidson Resilience Scale (CD-RISC)

Secondary Outcome Measures

Connor Davidson Resilience Scale (CD-RISC)
Occupational fatigue and recovery (OFER) scale
Acute fatigue and inter-shift recovery scales only
Occupational fatigue and recovery (OFER) scale
Acute fatigue and inter-shift recovery scales only
Professional Quality of Life (ProQOL5) scale
Professional Quality of Life (ProQOL5) scale
Perceived Stress Scale (PSS)
Perceived Stress Scale (PSS)
Occupational Coping Self-Efficacy Questionnaire for Nurses (OCSE-N).
Occupational Coping Self-Efficacy Questionnaire for Nurses (OCSE-N).
Mindfulness Attention Awareness Scale (MASS)
Mindfulness Attention Awareness Scale (MASS)
Mindfulness attention awareness will be measured using the Mindfulness Attention Awareness Scale (MASS).
Program Evaluation Outcomes for ARISE participants
For each component of the intervention, and for the ARISE program as a whole, we will ask participants to rate utility, satisfaction, and frequency of use of intervention components.
Program Evaluation Outcomes for ARISE participants
For each component of the intervention, and for the ARISE program as a whole, we will ask participants to rate utility, satisfaction, and frequency of use of intervention components.

Full Information

First Posted
January 9, 2017
Last Updated
April 16, 2018
Sponsor
Unity Health Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT03017469
Brief Title
Achieving Resilience in Acute Care Nurses (ARISE).
Official Title
Achieving Resilience in Acute Care Nurses (ARISE): A Randomized Controlled Trial of a Multi-component Intervention for Nurses in Critical Care and Trauma.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
February 21, 2017 (Actual)
Primary Completion Date
May 31, 2017 (Actual)
Study Completion Date
October 15, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Unity Health Toronto

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
Nurses are exposed to myriad stressors, both in the workplace and in their everyday lives, which can lead to adverse personal and professional outcomes. While workplace stress cannot be eliminated, nurses can learn techniques to build resilience, mitigate stress, and decrease fatigue. Organizational employee health, wellness, and assistance programs are all intentioned to provide this type of support; however, nurses often lack awareness of options and opportunities, and access can be a challenge. The purpose of the proposed study is to assess the outcomes of a multi-modal intervention and toolkit, ARISE, designed to enhance resilience and promote awareness of organizational resources for health, wellness, and employee assistance. We will evaluate the impact of participation in ARISE on resilience and other outcomes in nurses in critical care and trauma settings. As a Best Practice Spotlight Organization designated by the Registered Nurses Association of Ontario (RNAO), this project will incorporate relevant recommendations from Best Practice Guidelines (BPG) related to Workplace Health, Safety, and Well-being of the Nurse; and Preventing and Mitigating Nurse Fatigue in Health Care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress, Psychological, Compassion Fatigue
Keywords
Resilience, Workplace Stress, Occupational Fatigue, Compassion Fatigue, Peer Support, Self-Care, Employee Assistance

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ARISE Intervention
Arm Type
Experimental
Arm Description
Nurses who participate in the 1.5 day ARISE Intervention
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Nurses who do not participate in the ARISE Intervention
Intervention Type
Other
Intervention Name(s)
ARISE
Intervention Description
Full day (7.5 hours) workshop consisting of a resilience-focused seminar facilitated by our Employee Assistance Provider (EAP) [Shepell], an introduction to hospital based resources including EAP and health and wellness offerings, and an introduction to self-care and self-care techniques including yoga and stretches, stress relief using the senses and mindfulness Half day (3.75 hours) workshop focusing on the following self-care techniques: mindfulness, yoga and stretching, and creative and reflective reading and writing Peer support through social media engagement (closed Facebook group) for 3 months post-intervention participation Five online, instructor-guided mindfulness sessions (Zoom)
Primary Outcome Measure Information:
Title
Connor Davidson Resilience Scale (CD-RISC)
Time Frame
1 month post intervention
Secondary Outcome Measure Information:
Title
Connor Davidson Resilience Scale (CD-RISC)
Time Frame
3 months post intervention
Title
Occupational fatigue and recovery (OFER) scale
Description
Acute fatigue and inter-shift recovery scales only
Time Frame
1 month post intervention
Title
Occupational fatigue and recovery (OFER) scale
Description
Acute fatigue and inter-shift recovery scales only
Time Frame
3 months post intervention
Title
Professional Quality of Life (ProQOL5) scale
Time Frame
1 month post intervention
Title
Professional Quality of Life (ProQOL5) scale
Time Frame
3 months post intervention
Title
Perceived Stress Scale (PSS)
Time Frame
1 month post intervention
Title
Perceived Stress Scale (PSS)
Time Frame
3 months post intervention
Title
Occupational Coping Self-Efficacy Questionnaire for Nurses (OCSE-N).
Time Frame
1 month post intervention
Title
Occupational Coping Self-Efficacy Questionnaire for Nurses (OCSE-N).
Time Frame
3 months post intervention
Title
Mindfulness Attention Awareness Scale (MASS)
Time Frame
1 month post intervention
Title
Mindfulness Attention Awareness Scale (MASS)
Description
Mindfulness attention awareness will be measured using the Mindfulness Attention Awareness Scale (MASS).
Time Frame
3 months post intervention
Title
Program Evaluation Outcomes for ARISE participants
Description
For each component of the intervention, and for the ARISE program as a whole, we will ask participants to rate utility, satisfaction, and frequency of use of intervention components.
Time Frame
1 month post intervention
Title
Program Evaluation Outcomes for ARISE participants
Description
For each component of the intervention, and for the ARISE program as a whole, we will ask participants to rate utility, satisfaction, and frequency of use of intervention components.
Time Frame
3 months post intervention

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Nurse in the medical-surgical and trauma-neurosurgical intensive care units (MSICU and TNICU) and the medical/surgical floor (9CCN), full-time or part-time employment status, approval of clinical leader manager (CLM), receipt of written informed consent. Exclusion Crieria: casual employment status inability to attend intervention days
Facility Information:
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B1W8
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
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Achieving Resilience in Acute Care Nurses (ARISE).

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