Skip to main content
OpenTrials
Not yet recruiting

NCT Number: NCT07837193

Healthy Adaptation to Pregnancy, Postpartum and Parenthood

Healthy Adaptation to Pregnancy, Postpartum and Parenthood (HAP3) The HAP3 study is evaluating a new digital support program for pregnant women and their partners. The program includes the HAP3 Family App, which provides information and practical tools on healthy eating, physical activity, sleep, emotional well-being, pregnancy and postpartum care, healthy weight management, parenting, and child development.

Researchers want to find out whether the app is easy to use, acceptable to families, and practical to implement during pregnancy and after birth. The study will also explore whether using the app may help improve parents' mental well-being, healthy lifestyle habits, weight management, and early child development.

Participants will be randomly assigned to one of two groups. One group will receive access to the full HAP3 Family App, personalized coaching by phone or video call, and supportive messages. The other group will receive usual care and use the app only to complete study questionnaires.

The study will follow families from pregnancy until six months after birth. Participants will complete questionnaires about their health, well-being, and parenting experiences. Those using the full app will also be asked to complete brief in-app check-ins about mood, sleep, stress, and daily habits.

The HAP3 intervention is not a medical treatment and involves minimal risk. Potential benefits include increased awareness of health behaviors, access to evidence-based information, and support during the transition to parenthood.

The study is being conducted by researchers from KU Leuven (Belgium), Vrije Universiteit Amsterdam (Netherlands), and Technische Universität Dresden (Germany) as part of the European HAP3 project.

Not yet recruiting

Trial opening soon.

Get Notified

Key information

About this study

The Healthy Adaptation to Pregnancy, Postpartum and Parenthood (HAP3) study is a multicountry randomized controlled feasibility trial evaluating a digital intervention designed to support pregnant women and their partners during pregnancy and the first six months after birth. The study is conducted in Belgium, the Netherlands, and Germany.

The intervention consists of the HAP3 Family App and a supporting Dashboard used by the study team. The app provides evidence-based information and self-management tools covering nutrition, physical activity, sleep, emotional well-being, healthy weight management, pregnancy and postpartum care, parenting, and child development. Participants can engage with educational and interactive content tailored to their stage of pregnancy or postpartum period.

Participants assigned to the intervention group will have access to the full HAP3 Family App, brief video or telephone coaching sessions, personalized messages, and short in-app assessments that capture daily experiences such as mood, stress, sleep, appetite, and physical activity. Participants assigned to the control group will receive usual care and use a questionnaire-only version of the app.

The primary aim of the study is to evaluate the feasibility, usability, acceptability, and implementation of the HAP3 intervention and study procedures. This includes assessing recruitment and retention rates, participant engagement with the app, adherence to study procedures, data completeness, and user experiences.

Secondary objectives are exploratory and focus on potential effects of the intervention on parental mental well-being, healthy lifestyle behaviors, weight management, and early child development. Outcomes assessed include symptoms of anxiety, depression, stress, eating behavior, sleep quality, physical activity, social support, parent-child bonding, parental self-efficacy, and infant development during the first six months of life.

The HAP3 intervention is a non-invasive digital health program and is not intended to diagnose, treat, or replace routine medical care. The study is expected to provide important information about the practicality and acceptability of delivering integrated mental health, lifestyle, and parenting support through a digital platform during the transition to parenthood

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

HAP3 Family App

Behavioral

The HAP3 Family App is a multicomponent digital behavioral intervention designed specifically for pregnant women and their partners during pregnancy and the first six months postpartum. The intervention combines self-monitoring, self-management, evidence-based educational modules, Ecological Momentary Assessments (EMA), personalized dashboard messages, and structured video/telephone coaching. Content addresses multiple interconnected domains including mental well-being, healthy eating, physical activity, sleep, healthy weight management, pregnancy and postpartum care, parenting, and child development. Unlike interventions that focus on a single health outcome, the HAP3 intervention provides integrated support for both physical and mental health and actively involves partners. The intervention is delivered through a mobile application and supported by a dashboard that enables tailored feedback and coaching based on participant engagement and self-reported experiences.

Primary outcomes

  1. Participant Recruitment Rate

    Time frame: At enrollment (enrollment can be at any gestational age)

    Percentage of eligible participants who provide informed consent and are enrolled in the study.

  2. Participant Retention Rate

    Time frame: From enrollment until 6 months postpartum.

    Percentage of enrolled participants who complete the 6-month postpartum assessment.

  3. HAP3 Family App Acceptability

    Time frame: From enrollment until 6 months postpartum.

    Acceptability assessed using a study-specific questionnaire developed for the HAP3 feasibility study and informed by the Attitudes towards Psychological Online Interventions Questionnaire (APOI). The questionnaire evaluates participants' perceptions, satisfaction, and acceptance of the HAP3 Family App. Higher scores indicate greater acceptability of the intervention. The questionnaire is currently undergoing psychometric evaluation and has not yet been formally validated.

  4. HAP3 Family App Usability

    Time frame: From enrollment until 6 months postpartum.

    Usability measured using the mHealth App Usability Questionnaire (MAUQ). Scores range from 1 (Strongly agree) to 7 (Strongly disagree). A higher overall mean score (closer to 7.0) indicates a more favorable evaluation of the mobile health application's usability.

  5. Motivation for Eating Behavior Change

    Time frame: Baseline, 32 weeks pregnancy, and 6 months postpartum.

    Behavioural Change Towards Eating Behaviour (IBEB) questionnaire, a study-specific measure based on the Stages of Change framework. Higher scores indicate greater readiness and motivation to adopt healthy eating behaviors. A total score is calculated from the questionnaire items; score range will be determined following validation of the instrument.

  6. Motivation for Mental Health Behavior Change

    Time frame: Baseline, 32 weeks pregnancy, and 6 months postpartum.

    Evaluated using the University of Rhode Island Change Assessment (URICA) scale. The URICA is a 32-item questionnaire scored on a 5-point Likert scale (1 = Strongly Disagree, 5 = Strongly Agree). It measures four subscales representing stages of behavior change: Precontemplation, Contemplation, Action, and Maintenance.

    A composite Readiness to Change score is calculated using the formula: Contemplation + Action + Maintenance - Precontemplation. Composite scores typically range from a minimum of -2 to a maximum of 14. Higher composite scores indicate a greater readiness and overall motivation to change the target behavior.

Secondary outcomes

  1. Edinburgh Postnatal Depression Scale (EPDS)

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, and 6 months postpartum.

    Depressive symptoms assessed using the Edinburgh Postnatal Depression Scale (EPDS). Total scores range from 0 to 30, with higher scores indicating more severe depressive symptoms.

  2. 6-item State-Trait Anxiety Inventory (STAI-6)

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Anxiety symptoms assessed using the 6-item State-Trait Anxiety Inventory (STAI-6). Scores range from 20 to 80 after score transformation, with higher scores indicating greater anxiety.

  3. Depression Anxiety Stress Scales, Stress Subscale (DASS-21)

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    tress symptoms assessed using the Stress subscale of the Depression Anxiety Stress Scales-21 (DASS-21). Subscale scores range from 0 to 42 after standard scoring, with higher scores indicating greater stress.

  4. Pregnancy-related Anxiety Questionnaire-Revised 2 (PRAQ-R2)

    Time frame: 32 weeks pregnancy.

    Assessed using the Pregnancy-related Anxiety Questionnaire-Revised 2 (PRAQ-R2). The PRAQ-R2 is a 10-item self-report questionnaire scored on a 5-point Likert scale. Total scores are calculated by summing all items and range from a minimum of 10 to a maximum of 50. Higher scores indicate greater pregnancy-related anxiety.

  5. Paternal Pregnancy-related Anxiety Scale (PPrAS)

    Time frame: 32 weeks pregnancy.

    Pregnancy-related anxiety among partners assessed using the Paternal Pregnancy-related Anxiety Scale (PPrAS). Higher scores indicate greater pregnancy-related anxiety.

  6. Maternal and Partner Weight

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Body weight measured in kilograms (kg) using standardized measurements at study visits and self-reported weight between visits (used for gastational weight gain (GWG) and postpartum weight retention (PPWR))

  7. Maternal and Partner Body Composition

    Time frame: Baseline and 6 months postpartum.

    Body composition assessed using Bioelectrical Impedance Analysis (BIA).

  8. Eating Behavior

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    The Three-Factor Eating Questionnaire-Revised 18-item (TFEQ-R18) evaluates three distinct domains of eating behavior: Cognitive Restraint (6 items evaluating conscious restriction of food intake to control weight), Uncontrolled Eating (9 items evaluating the tendency to lose control over eating when triggered by food cues), and Emotional Eating (3 items evaluating overeating in response to negative mood states). Raw item responses for each subscale are summed and linearly transformed to a standardized 0 to 100 scale. The overall outcome reports three separate subscale scores ranging from 0 to 100, where higher scores indicate greater cognitive control over food intake, a higher tendency to overeat impulsively, or a greater likelihood of eating in response to negative emotions, respectively.

  9. Body Image

    Time frame: 32 weeks pregnancy and 6 months postpartum.

    The Body Image in Pregnancy and Postpartum Scale (BIPPS) evaluates multi-dimensional maternal body image dissatisfaction and physical anxieties distinct to the perinatal period. Individual questionnaire items are scored on a 5-point Likert scale (ranging from 1 to 5) and aggregated to generate an overall composite total score. Total scores range from 20 to 100, where higher scores indicate greater body image concerns, reflecting increased dissatisfaction or distress regarding physical appearance and structural bodily changes during pregnancy or postpartum phases.

  10. Infant weight

    Time frame: 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Infant weight measured in kilograms (kg). Higher values indicate greater infant weight.

  11. Infant length

    Time frame: 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Infant length measured in centimeters (cm). Higher values indicate greater infant length.

  12. APGAR Score

    Time frame: at birth

    Neonatal health status assessed using the APGAR score. Total scores range from 0 to 10, with higher scores indicating better neonatal health and adaptation after birth.

  13. Infant Development

    Time frame: 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Infant development assessed using the Infant Development Inventory (IDI), a parent-reported measure of developmental attainment across the domains of language, self-help, motor, and social development. Higher scores indicate more advanced developmental attainment. The score range depends on the age-specific version administered.

  14. Infant temperament

    Time frame: 3 months postpartum.

    Infant temperament assessed using the Infant Behavior Questionnaire-Revised Very Short Form (IBQ-R VSF) Negative Reactivity Subscale. Scores range from 1 to 7, with higher scores indicating greater infant negative reactivity, including distress, fearfulness, and difficulty in emotional regulation.

  15. Body Height

    Time frame: Baseline and 6 months postpartum.

    Body height measured in centimeters (cm) using standardized measurement procedures. Higher values indicate greater body height.

Other outcomes

  1. Health, Lifestyle, and Parenting-Related Outcomes

    Time frame: Baseline, 32 weeks pregnancy, 6 weeks postpartum, 3 months postpartum, and 6 months postpartum, depending on the specific measure.

    Exploratory assessment of factors associated with parental and child well-being, including sleep quality, physical activity, social support, body image, eating behaviors, parent-child bonding, parental self-efficacy, and birth-related post-traumatic stress symptoms using validated questionnaires (PSQI, PPAQ, OSSS-3, BIPPS, TFEQ, PPBS, SENR, and City BiTS-SF).

  2. Sleep Quality

    Time frame: 32 weeks pregnancy, 6 weeks postpartum, and 6 months postpartum.

    Sleep quality assessed using the Pittsburgh Sleep Quality Index (PSQI). Total scores range from 0 to 21, with higher scores indicating poorer sleep quality. A global score >5 is commonly used to indicate poor sleep quality.

  3. Physical activity

    Time frame: Baseline, 32 weeks pregnancy, and 6 months postpartum

    Physical activity assessed using the Pregnancy Physical Activity Questionnaire-Short Form (PPAQ-SF). Scores are calculated as Metabolic Equivalent of Task (MET)-hours per week across activity domains. Higher scores indicate greater physical activity levels. No fixed minimum or maximum score is defined because scores depend on the participant's reported activity.

  4. Social support

    Time frame: Baseline, 6 weeks postpartum, and 6 months postpartum.

    Social support assessed using the Oslo Social Support Scale (OSSS-3). Total scores range from 3 to 14, with higher scores indicating greater perceived social support. Scores of 3-8 indicate poor support, 9-11 indicate moderate support, and 12-14 indicate strong support.

  5. Childbirth-Related Posttraumatic Stress Symptoms

    Time frame: 6 weeks postpartum.

    Childbirth-related posttraumatic stress symptoms assessed using the City Birth Trauma Scale Short Form (City BiTS-SF). Total scores range from 0 to 24, with higher scores indicating more severe childbirth-related posttraumatic stress symptoms.

  6. Parent-Child Bonding

    Time frame: 32 weeks pregnancy, 6 weeks postpartum, and 6 months postpartum

    Parent-child bonding assessed using the Pre- and Postnatal Bonding Scale (PPBS). Total scores range from 8 to 40, with higher scores indicating stronger parent-child bonding.

  7. Parental Self-Efficacy

    Time frame: 32 weeks pregnancy and 3 months postpartum

    Parenting self-efficacy assessed using the Self-Efficacy in the Nurturing Role (SENR) questionnaire. Total scores range from 16 to 112, with higher scores indicating greater parental self-efficacy in the nurturing role.

  8. Perinatal Events and Pathology

    Time frame: 6 weeks postpartum.

    Perinatal events and pregnancy-, birth-, and postpartum-related pathology assessed using study-specific questions. Outcomes include the occurrence of maternal, fetal, neonatal, and obstetric complications. Higher scores are not inherently better or worse as responses consist of categorical clinical events and conditions.

  9. Postpartum Experience

    Time frame: 6 weeks postpartum, 3 months postpartum, and 6 months postpartum.

    Postpartum experience assessed using study-specific questions regarding breastfeeding and postpartum pain. Outcomes include breastfeeding status and pain-related experiences. Higher scores are not inherently better or worse because responses may be categorical or item-specific.

Study contacts

Contact information is provided by the study sponsor or research team.

Annick Bogaerts Prof. Dr., Prof. Dr.

CONTACT

[email protected]

Annick Bogaerts

Sponsors and collaborators

Lead sponsor

KU Leuven

Other

Collaborators

  • Technische Universität Dresden
  • University of Aarhus
  • University of Dublin, Trinity College
  • VU University of Amsterdam

Registry information

Official study 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

Acronym: HAP3

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Sep 23, 2026
Registry last updated
Sep 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.