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

NCT ID: NCT03213327

Last Updated: 2020-06-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

174 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-07-10

Study Completion Date

2019-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Mental Health Disorder

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

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.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Case management

Case management program Utilization of the StayOk web application

Group Type OTHER

StayOk web application

Intervention Type DEVICE

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

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

16 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Health and Medical Services

UNKNOWN

Sponsor Role collaborator

Helsana

UNKNOWN

Sponsor Role collaborator

Neomentum

UNKNOWN

Sponsor Role collaborator

Sanatorium Kilchberg AG

OTHER

Sponsor Role collaborator

Design your life

UNKNOWN

Sponsor Role collaborator

Zurich University of Applied Sciences

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Aureliano Crameri

Dr. phil.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Agnes von Wyl, Prof

Role: PRINCIPAL_INVESTIGATOR

Zurich University of Applied Sciences

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Helsana

Zurich, , Switzerland

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Switzerland

References

Explore related publications, articles, or registry entries linked to this study.

Derogatis LR, Melisaratos N. The Brief Symptom Inventory: an introductory report. Psychol Med. 1983 Aug;13(3):595-605.

Reference Type BACKGROUND
PMID: 6622612 (View on PubMed)

Jenny GJ, Bauer GF, Vinje HF, Vogt K, Torp S. The Application of Salutogenesis to Work. 2016 Sep 3. In: Mittelmark MB, Sagy S, Eriksson M, Bauer GF, Pelikan JM, Lindstrom B, Espnes GA, editors. The Handbook of Salutogenesis [Internet]. Cham (CH): Springer; 2017. Chapter 20. Available from http://www.ncbi.nlm.nih.gov/books/NBK435821/

Reference Type BACKGROUND
PMID: 28590629 (View on PubMed)

Damasio BF, Valentini F, Nunes-Rodriguez SI, Kliem S, Koller SH, Hinz A, Brahler E, Finck C, Zenger M. Is the General Self-Efficacy Scale a Reliable Measure to be used in Cross-Cultural Studies? Results from Brazil, Germany and Colombia. Span J Psychol. 2016 May 26;19:E29. doi: 10.1017/sjp.2016.30.

Reference Type BACKGROUND
PMID: 27225231 (View on PubMed)

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BASEC-Nr. 2016-00879

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Student Wellness 2.0
NCT06804213 COMPLETED NA
I-ACT With Check Yourself
NCT02764190 COMPLETED NA
Working Toward Wellness
NCT00694681 COMPLETED NA
New Technology and Child Health
NCT02622035 COMPLETED NA