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Clinical Trials/NCT05607758
NCT05607758
Active, not recruiting
Not Applicable

Digital Stress Management Intervention for Health Care Providers

Oslo University Hospital1 site in 1 country117 target enrollmentNovember 10, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Health Care Providers
Sponsor
Oslo University Hospital
Enrollment
117
Locations
1
Primary Endpoint
The Perceived Stress Scale (PSS-14)
Status
Active, not recruiting
Last Updated
11 months ago

Overview

Brief Summary

The purpose with this study is to test if the app-based stress management program StressProffen, can be of interest and support for stress management among health care providers.

Detailed Description

For health care providers, work-related stress can be a major challenge that can lead to frustration, lower motivation, reduced quality of life and burnout, and the last year's COVID-19 pandemic particularly emphasized the challenges in the stressful everyday life faced by health care providers. There are, however, interventions that can be of support, both for the prevention of stress and for coping with stress in challenging situations, and in recent years there has also been an increased focus on stress in working life in this setting. Several studies have also recently been carried out which aim to deliver such interventions via applications (apps) to promote employees' physical and mental health, as well as their ability to cope with stress. However, there is a need for more research in the field, especially with a focus that content in such apps should be based on evidence-based theory, and that interviews and a similar qualitative approach should be included in studies to gain increased insight into the need for and usefulness of digital tools among health care providers. This study will therefore test the effect of an app-based program for stress management, StressProffen, among health care providers, in a single arm study. The app contains 10 modules distributed over four weeks, focusing on education of different techniques for reduction of stress and stress reduction exercises. StressProffen was initially developed and tested for stress management in patients with cancer, with good results. Among other things, a randomized controlled trial showed a statistically significant reduction in perceived stress, anxiety, depression and self-regulation fatigue, as well as increased health-related quality of life, for participants in the intervention group compared to the control group. The aim of this study is to test whether StressProffen can be of interest and support for stress management among health care providers.

Registry
clinicaltrials.gov
Start Date
November 10, 2022
End Date
July 31, 2025
Last Updated
11 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Elin Børøsund

Principal Investigator

Oslo University Hospital

Eligibility Criteria

Inclusion Criteria

  • Health care providers (included but not restricted to, registered nurses, physicians, physiotherapists, occupational therapists, dietitians, social workers, health workers).
  • Working with patient treatment or follow up at Oslo University Hospital
  • Having their own smart phone or tablet
  • Being able to write/read/speak Norwegian

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

The Perceived Stress Scale (PSS-14)

Time Frame: Change from baseline to f-up month 6

14 item scale measuring perceived stress. Scale range: 0-56. Higher scores indicate higher perceived stress.

Secondary Outcomes

  • The Self-Regulatory Fatigue-18 (SRF-18)(Change from baseline to f-up month 6)
  • The Hospital Anxiety and Depression Scale (HADS)(Change from baseline to f-up month 6)
  • SF-36 Item Short Form Health Survey (RAND-36 version)(Change from baseline to f-up month 6)

Study Sites (1)

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