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Achieving Resilience in Acute Care Nurses (ARISE).

U

Unity Health Toronto

Status

Completed

Conditions

Compassion Fatigue
Stress, Psychological

Treatments

Other: ARISE

Study type

Interventional

Funder types

Other

Identifiers

NCT03017469
SMH30Dec2016

Details and patient eligibility

About

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.

Enrollment

29 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

29 participants in 2 patient groups

ARISE Intervention
Experimental group
Description:
Nurses who participate in the 1.5 day ARISE Intervention
Treatment:
Other: ARISE
Control Group
No Intervention group
Description:
Nurses who do not participate in the ARISE Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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