Usability Study of Gestational and Postpartum Weight Management Program
Recruiting
Observational Study
Pregnancy
Postpartum
Obese Pregnant Women
Weight Management
Digital Intervention
Usability
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Observational
- Participants needed
- 30 (estimated)
- Sponsor
- Turku University Hospital · Government
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
The principal aim of this study is to evaluate the usability of the Hope-D gestational and 6 months postpartum weight management program. We will evaluate the usability, functionality, and acceptability of the developed Hope-D weight management program that includes digital pathway for weight management, general or individual weight management plan and individual or group coaching for weight manag…
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria:
* General pregnant women with prepregnancy BMI at least 30 kg/m2
* Competence in using the digital care pathway and electronic maternity card
Exclusion Criteria:
\- Significant difficulty in cooperating (e.g. inadequate Finnish language skills)
Contacts