Healthy Adaptation to Pregnancy, Postpartum and Parenthood

NCT ID
NCT07837193
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
KU Leuven
Conditions
Child Development, Gestational Weight Gain, Perinatal Mental Health, Postpartum Weight Retention

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Healthy Adaptation to Pregnancy, Postpartum and Parenthood (HAP3) Feasibility Study of the HAP3 Family App and Dashboard Targeting Health Behaviours for Weight and Mental Health in Women, Partners, and Offspring During Pregnancy and Postpartum

Enrollment: 572 participants (Estimated).

What is being studied

  • Behavioral: HAP3 Family App

Who may be eligible

Ages
Not specified in the registry data
Sex
All
Healthy volunteers accepted
Yes

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Pregnant person aged 18 years or older. * Currently pregnant (participants may be recruited at any stage of pregnancy, -although recruitment before 16 weeks of pregnancy is preferred). * Sufficient proficiency in Dutch, German, or English. * Resident of Belgium, the Netherlands, or Germany. * Able and willing to provide informed consent. Partners: * Partner of an eligible pregnant participant. * Aged 18 years or older. * Sufficient proficiency in Dutch, German, or English. * Resident of Belgium, the Netherlands, or Germany. * Able and willing to provide informed consent. Exclusion Criteria: * Current suicidal ideation. * Severe mental health disorder (e.g., bipolar disorder, schizophrenia, borderline personality disorder). * Severely debilitating physical health condition that substantially affects daily functioning (e.g., advanced cardiovascular disease, advanced respiratory disease, or active cancer). * History of or planned bariatric surgery during the study period. * Failure or unwillingness to provide informed consent. * Current participation or planned enrollment in another clinical trial that may conflict with this study.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Belgium

Sample of listed locations

  • Vrouw en Kind — Leuven, 3000, Belgium — Site recruitment status not specified in the registry data

Study details

Start date
September 1, 2026
Primary completion date
May 1, 2029
Completion date
May 1, 2029
First posted
September 23, 2026
Collaborators
Technische Universität Dresden, University of Aarhus, University of Dublin, Trinity College, VU University of Amsterdam

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07837193
Registry last updated
September 23, 2026
QualifiedStudies registry data refreshed
September 28, 2026
QualifiedStudies record fetched
September 28, 2026

View NCT07837193 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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