Skip to main content
OpenTrials
Completed

NCT Number: NCT03213327

StayOK - an Innovative Measuring Instrument for the Early Identification and Treatment of Psychosocial Risks

The validity and the sensitivity of different measures implemented in the web application StayOk are investigated. The measures are used primarily for the assessment and the early identification of psychosocial risks. Secondarily, the results of the assessment are applied to generate health-promoting advices for the user of the web application.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Mental Health Disorder Behavior Mental Disorders Personal Satisfaction Psychological Well-Being

Age range

16 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Helsana

Zurich, Switzerland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • at 16 years of age
  • mild to moderate psychological distress

Exclusion criteria

  • serious cognitive impairment due to dementia or cerebrovascular insult
  • Insufficient knowledge of one of the following languages: German, French, Italian or English

Treatment and study plan

StayOk web application

Device

Patients fill in the questionnaires of the web application and receive an analyzed profile of their psychosocial condition and health-promoting advices

Primary outcomes

  1. Psychological distress

    Time frame: 0 week (first assessment)

    The psychological distress is assessed by the Brief Symptom Inventory (BSI; Derogatis & Melisaratos, 1983)

  2. Work-related sense of coherence

    Time frame: 0 weeks

    The work-related sense of coherence is assessed by the Work Sense of Coherence (W-SoC 9; Jenny et al., 2016)

  3. Perceived self-efficacy

    Time frame: 0 weeks

    This aspect is measure by the General Self-Efficacy Scale (GSE; Damásio et al., 2016)

Secondary outcomes

  1. Effectiveness of health-promoting advices

    Time frame: 12 weeks after the first assessment

    The effectiveness of the advices generated by the software is assessed by means of a self-developed questionnaire: Participants are inquired as to (1) whether they put in practice the advices and (2) how they evaluate the benefit of the applied advices and the consequent satisfaction.

Sponsors and collaborators

Lead sponsor

Zurich University of Applied Sciences

Other

Collaborators

  • Design your life
  • Health and Medical Services
  • Helsana
  • Neomentum
  • Sanatorium Kilchberg AG

Registry information

Acronym: StayOK

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 11, 2017
Registry last updated
Jun 23, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.