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Digital Stress Management Intervention for Health Care Providers

Digital Stress Management Intervention for Health Care Providers

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05607758
Enrollment
117
Registered
2022-11-07
Start date
2022-11-10
Completion date
2025-07-31
Last updated
2025-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Care Providers, Psychological, Stress

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.

Interventions

BEHAVIORALStressProffen©™

An app-based program for stress management consisting of 10 modules that teaches stress management, cognitive behavioral coping skills and relaxation training.

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

* None

Design outcomes

Primary

MeasureTime frameDescription
The Perceived Stress Scale (PSS-14)Change from baseline to f-up month 314 item scale measuring perceived stress. Scale range: 0-56. Higher scores indicate higher perceived stress.

Secondary

MeasureTime frameDescription
The Hospital Anxiety and Depression Scale (HADS)Change from baseline to f-up month 314 item scale measuring anxiety and depression. The Scale has a total score with a scale range of 0 to 42 and an anxiety (HADS-A) and a depression (HADS-D) subscale, both with scale range of 0 to 21. Sub scale scores: 0-7= Normal, 8-10= Borderline abnormal (borderline case), 11-21= abnormal (case).
SF-36 Item Short Form Health Survey (RAND-36 version)Change from baseline to f-up month 336 item scale measuring health related quality of life (HRQoL). The scale has 8 subscales and 1 single item score. Scale and single item range: 0 to 100. Higher scores indicate higher HRQoL.
The Self-Regulatory Fatigue-18 (SRF-18)Change from baseline to f-up month 318 item scale measuring self-regulation. Scale range: 18 to 90. A higher score indicates higher self-regulatory fatigue

Other

MeasureTime frameDescription
Intervention commentary3 monthsA six item brief measure of participant's intervention reactions. The first 3 items gauged participants' program perception on a scale from 1 to 5, with 5 indicating better perception. The next 3 items were open ended questions: \* What did you like best? \* What did you like the least? \* Suggestions for improvement?
SleepChange from baseline to f-up month 3Four questions related to number of hours of sleep per 24 hours, how much sleep participants need to feel rested, experienced quality of sleep an impact of shift-work on sleep

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026