Supporting Lifestyle Changes After Delivery
Recruiting
N/A
Interventional Study
Obesity, Maternal
Lifestyle
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 200 (estimated)
- Sponsor
- Oulu University Hospital · Other
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About This Trial
Use of information and communication technology -based health behavior change support system in modifying lifestyle after delivery among women with obesity.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pre-pregnancy BMI ≥ 30.0 kg/m\^2
* Smartphone user
Exclusion Criteria:
* Eating disorder
* Severe mental disorder
* Use of other lifestyle support system or medication
* Non-Finnish speaker
Contacts