Kogito: App to Reduce Perinatal Psychosocial Stress

Status Recruiting

Clinical Trial Summary

The purpose of this research study is to test the efectivness of the remote solution for psychosocial stress in pregnant women and postpartum women. Based on the connection of know-how in the field of social sciences and humanities (psychology, volunteer community and peer work with target group) and technological know-how (software design and development), investigators developed an interactive intervention software (Kogito app) to reduce psychosocial stress in the target group.

Clinical Trial Description

This study examine the potential of Kogito app in the delivery of mental and social support care to pregnant and postpartum women using psychometric methods. A) Clinical efficacy of Kogito app in a clinical cohort. Sample: pregnant or postpartum women with who are being treated in the psychiatric perinatal outpatient clinic of the National Institute of Mental Health, Czech Republic. The app will be tested as a add-on method of care. Intervention group: Kogito app is added to the usual care Control group: usual care Randomization: 1:1 Participants in the intervention group will be asked to do following things: 1. complete survey questions at entrance into the study 2. use the kogito app 3. complete survey questions one month after study entrance Participants in the control group will be asked to do following things: 1. complete survey questions at entrance into the study 2. complete survey questions one month after study entrance B) Clinical efficacy of the Kogito app in a general cohort. The app will be offered free of charge to users from the population of pregnant and postpartum women for the duration of the study. Recruitment method: advertisements on social networks of National Institute of Mental Health and other public media in Czechia Sample: pregnant or postpartum women from general population in Czechia. The app will be tested using the waiting list as a control condition. Intervention group: Kogito app Control group: one month waiting list Randomization: 1:1 Participants in the intervention group will be asked to do following things: 1. complete survey questions at entrance into the study 2. use the kogito app 3. complete survey questions one month after study entrance Participants in the control group will be asked to do following things: 1. complete survey questions at entrance into the study 2. complete survey questions one month after study entrance ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04876144
Study type	Interventional
Source	National Institute of Mental Health, Czech Republic
Contact	Pavla Spadova
Phone	+420 283 088 436
Email	pavla.spadova@nudz.cz
Status	Recruiting
Phase	N/A
Start date	July 28, 2021
Completion date	December 31, 2021

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