Usability Study of Gestational and Postpartum Weight Management Program
Recruiting · NCT07272824 · Observational (researchers observe without assigning treatment) · Lead sponsor: Turku University Hospital
View the official record on ClinicalTrials.gov →What this trial is about
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 management from pregnancy to 6 months postpartum.
Who can take part
Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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)
Where it is running
1 location listed.
- The wellbeing services county of Southwest Finland - Turku, Finland, Finland