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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03213327
Acronym
StayOK
Enrollment
174
Registered
2017-07-11
Start date
2017-07-10
Completion date
2019-07-31
Last updated
2020-06-23

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

Conditions

Mental Health Disorder

Keywords

mental health, assessment, health promotion, case management, health insurance

Brief summary

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.

Interventions

DEVICEStayOk web application

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

Sponsors

Health and Medical Services
CollaboratorUNKNOWN
Helsana
CollaboratorUNKNOWN
Neomentum
CollaboratorUNKNOWN
Sanatorium Kilchberg AG
CollaboratorOTHER
Design your life
CollaboratorUNKNOWN
Zurich University of Applied Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Patients are examined at two time points: baseline and 12 weeks after the Intervention. The Intervention consists of health-promoting advices provided by the software algorithm. The effect of this intervention is evaluated 12 weeks after.

Eligibility

Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Psychological distress0 week (first assessment)The psychological distress is assessed by the Brief Symptom Inventory (BSI; Derogatis & Melisaratos, 1983)
Work-related sense of coherence0 weeksThe work-related sense of coherence is assessed by the Work Sense of Coherence (W-SoC 9; Jenny et al., 2016)
Perceived self-efficacy0 weeksThis aspect is measure by the General Self-Efficacy Scale (GSE; Damásio et al., 2016)

Secondary

MeasureTime frameDescription
Effectiveness of health-promoting advices12 weeks after the first assessmentThe 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.

Countries

Switzerland

Outcome results

None listed

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