Supporting Lifestyle Changes After Delivery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorOulu University Hospital
About this trial
Use of information and communication technology -based health behavior change support system in modifying lifestyle after delivery among women with obesity.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Pre-pregnancy BMI ≥ 30.0 kg/m²
Smartphone user
Disqualifiers
Eating disorder
Severe mental disorder
Use of other lifestyle support system or medication
Non-Finnish speaker
Trial design
Design model
Parallel
Treatments tested in this trial
Information and communication technology -based health behavior change support system
DeviceInformation and communication technology -based health behavior change support system addition to conventional postpartum lifestyle education
Treatment groups
200 Participants
are divided into 2 treatment groupsGroup A: InterventionExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Weight change
Weight change in kilograms and change of body mass index (kg/m\^2)
Time frame
12 months2
Weight change
Weight change in kilograms and change of body mass index (kg/m\^2)
Time frame
24 monthsSecondary outcomes
1
Weight change before subsequent pregnancy
Weight change in kilograms and change of body mass index (kg/m\^2)
Time frame
1-8 years2
Pregnancy disorders in subsequent pregnancy (gestational diabetes, pre-eclampsia, gestational hypertension, preterm delivery)
Number of participants with pregnancy disorders in subsequent pregnancy (gestational diabetes, pre-eclampsia, gestational hypertension, preterm delivery, mortality)
Time frame
1-8 years3
Neonatal outcome in subsequent pregnancy (preterm birth, large for gestational age, small for gestational age, need for neonatal intensive care, mortality)
Number of neonates with adverse neonatal outcome (preterm birth, large for gestational age, small for gestational age, need for neonatal intensive care, mortality)
Time frame
1-8 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Oulu University Hospital
Lead sponsor
University of Oulu
Collaborator
Source ClinicalTrials.gov