Viewing Study NCT06495801



Ignite Creation Date: 2024-07-17 @ 11:05 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06495801
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-11
First Post: 2024-07-02

Brief Title: Effectiveness of a Mobile Application in Improving Employees Social Well-being
Sponsor: University of Eastern Finland
Organization: University of Eastern Finland

Study Overview

Official Title: Työntekijöiden Sosiaalisen Hyvinvoinnin lisääminen Mobiilisovelluksen Avulla Effectiveness of a Mobile Application in Improving Employees Social Well-being
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this cluster randomized controlled trial is to learn if using Frendie PRO mobile application at workplaces improves social well-being in employees The main questions it aims to answer are

Does using Frendie PRO mobile application at work for 6 months reduce loneliness in employees Does using Fendie PRO mobile application at work for 6 months reduce social isolation in employees

Researchers will compare employees from workplaces that use the Frendie PRO mobile application to employees from workplaces that do not use the mobile application to see if there are differences in their levels of social well-being loneliness social isolation perceived social support depressive symptoms

Participants will be given access to the Frendie PRO mobile application and encouraged to use it by employers
Detailed Description: Participants will be recruited from workplaces that use the Frendie PRO mobile application After collecting baseline data each workplace will be randomly assigned to treatment or control conditions The unit of randomization is a workplace or a team or department in bigger organizations

The intervention group will be encouraged to download and start using the Frendie PRO mobile application The control group will be informed of the date when they will have access to it six months after the baseline

Both groups are asked to participate in two follow-ups - a 3-month follow-up and a 6-month follow-up

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None