StayOK - an Innovative Measuring Instrument for the Early Identification and Treatment of Psychosocial Risks (StayOK)
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|ClinicalTrials.gov Identifier: NCT03213327|
Recruitment Status : Recruiting
First Posted : July 11, 2017
Last Update Posted : July 11, 2017
|Condition or disease||Intervention/treatment|
|Mental Health Disorder||Device: StayOk web application|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||350 participants|
|Intervention Model:||Single Group Assignment|
|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.
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||StayOK - an Innovative Measuring Instrument for the Early Identification and Treatment of Psychosocial Risks|
|Actual Study Start Date :||July 10, 2017|
|Estimated Primary Completion Date :||December 31, 2018|
|Estimated Study Completion Date :||March 31, 2019|
Case management program Utilization of the StayOk web application
Device: StayOk web application
Patients fill in the questionnaires of the web application and receive an analyzed profile of their psychosocial condition and health-promoting advices
- Psychological distress [ Time Frame: 0 week (first assessment) ]The psychological distress is assessed by the Brief Symptom Inventory (BSI; Derogatis & Melisaratos, 1983)
- 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)
- Perceived self-efficacy [ Time Frame: 0 weeks ]This aspect is measure by the General Self-Efficacy Scale (GSE; Damásio et al., 2016)
- 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03213327
|Contact: Ursula Büsser, MSc||+41 79 957 11 email@example.com|
|Contact: Ebru Tekol|
|Principal Investigator:||Agnes von Wyl, Prof||Zurich University of Applied Sciences|