With this study the investigators aim to examine through a mixed method study the feasibility, usability and satisfaction with the developed online tool for perinatal mental health problems. This will be done through a pre- and post measurement of depressive and anxiety symptoms and the use of the tool itself. In addition, a qualitative thematic analysis will be conducted on the clarity, understandability and user-friendliness of the tool.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
use of the online tool, by means of time logged in
Timeframe: up to 10 weeks
use of the online tool, by means of number of log-ins
Timeframe: up to 10 weeks
use of the online tool, by means of number of lesson/modules started
Timeframe: up to 10 weeks
use of the online tool, by means of number of exercises completed
Timeframe: up to 10 weeks
usability of the online tool, by means of the System Usability Scale (SUS), when participant completes the program
Timeframe: through study completion, after each module (up to 10 wks)
usability of the online tool, by means of the System Usability Scale (SUS) when participant no longer logs in and after invitation through email reminder
Timeframe: 2 weeks
usability of the online tool, by means of an open-ended qualitative question when participant completes the program.
Timeframe: through study completion, after each module (up to 10 wks)
usability of the online tool, by means of an open-ended qualitative question, when participant no longer logs in and after invitation through email reminder
Timeframe: 2 weeks
patient satisfaction, by means of qualitative questions when participant completes the program
Timeframe: through study completion, after each module (up to 10 wks)
patient satisfaction, by means of open-ended qualitative questions, when participant completes the program
Timeframe: through study completion, after each module (up to 10 wks)
patient satisfaction, by means of qualitative questions when participant no longer logs in, and after invitation through email reminder
Timeframe: 2 weeks
patient satisfaction, by means of open-ended qualitative questions when participant no longer logs in and after invitation through email reminder
Timeframe: 2 weeks