NCT05607758

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
117

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 2, 2022

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 7, 2022

Completed
3 days until next milestone

Study Start

First participant enrolled

November 10, 2022

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 16, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
Last Updated

May 28, 2025

Status Verified

May 1, 2025

Enrollment Period

2.5 years

First QC Date

November 2, 2022

Last Update Submit

May 27, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • The Perceived Stress Scale (PSS-14)

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

    Change from baseline to f-up month 3

  • The Perceived Stress Scale (PSS-14)

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

    Change from baseline to f-up month 6

Secondary Outcomes (6)

  • The Hospital Anxiety and Depression Scale (HADS)

    Change from baseline to f-up month 3

  • 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 3

  • SF-36 Item Short Form Health Survey (RAND-36 version)

    Change from baseline to f-up month 6

  • The Self-Regulatory Fatigue-18 (SRF-18)

    Change from baseline to f-up month 3

  • +1 more secondary outcomes

Other Outcomes (3)

  • Intervention commentary

    3 months

  • Sleep

    Change from baseline to f-up month 3

  • Sleep

    Change from baseline to f-up month 6

Study Arms (1)

App for Stress management

EXPERIMENTAL

Participants will: * Participate in a physical introduction to the app-based stress management program * Get access to the app-based program, and a new module every third day (total 10 modules). The app consists of stress management education, cognitive behavioral interventions and relaxation training exercises. * Receive two phone follow-up calls from study personnel (about 3 and 6 weeks after the physical introduction)

Behavioral: StressProffen©™

Interventions

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

Also known as: Stress Management
App for Stress management

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Oslo University hospital

Oslo, 0588, Norway

Location

Study Officials

  • Lise Solberg Nes, PhD

    Oslo University Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 2, 2022

First Posted

November 7, 2022

Study Start

November 10, 2022

Primary Completion

May 16, 2025

Study Completion

July 31, 2025

Last Updated

May 28, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations