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Recruiting NCT05870878

Generation R Next - Optimaal Opgroeien

No phase Interventional Pregnancy Early Outcome, Adverse Birth Lifestyle Factors Preconception Care

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Standard care, Lifestyle program.
Who it may be relevant to
Registry conditions: Pregnancy Early, Outcome, Adverse Birth, Lifestyle Factors, Preconception Care. Basic parameters: No limits · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Netherlands
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of this randomized controlled trial is to improve birth outcomes and long-term outcomes in mother and child by optimizing lifestyle,nutrition and stress experience in the preconception period and early pregnancy in women and men The main research question that will be addressed is: Does an intervention focused on optimizing preconception and early pregnancy lifestyle, nutrition and stress improve the birth outcomes and long-term outcomes in mother and child? Participants will receive an individual lifestyle consultation at the start of the study. Depending on their study arm, participants will receive an additional lifestyle program focused on health during preconception and early pregnancy, coping with stress and adherence to a healthy(er) lifestyle. The given advices are based on national guidelines. Researchers will compare the intervention group and control group to see if (adherence to) this lifestyle program improve birth outcomes and long-term outcomes in mother and child.

Detailed description

Preconception and early pregnancy are critical periods for health and wellbeing across the full life course in the offspring. Improving lifestyle, nutrition and stress in both women and their partners already from the preconception period onwards may have beneficial effects on the offspring.

This RCT will include preconception/early pregnancy integrated life style intervention focused on a healthy weight (BMI: 18.5-25 kg/m2), stopping alcohol/smoking/drugs, supplementing folic acid and vitamin D, a healthy diet (weekly fish, iron and vitamin C rich food) and stress reduction. Reducing stress appears to be effective for improving (maternal) health and reducing risk behavior. Mind-body therapy, a combination of yoga exercises and mindfulness seems to be a popular intervention, especially among pregnant women or women of childbearing age from various ethnic backgrounds.

The use of the preconception consultation is not yet optimal. This is partly due to the difficulty of reaching (vulnerable) groups and the limited insight regarding the efficacy.

The aim of this randomized controlled trial is to improve birth outcomes and long-term outcomes in mother and child by optimizing lifestyle in the preconception period and early pregnancy in women and men. The main research question is whether an intervention focused on optimizing preconception and early pregnancy lifestyle, nutrition and stress improves the birth outcomes and long-term outcomes in mother and child?

This RCT will be embedded in the available Generation R Next research infrastructure.

Prior to randomization, the intervention and control groups will be offered an individual lifestyle consultation for both women and men, and, if pregnant, an early pregnancy ultrasound. After randomization, there will be two groups: the intervention group and the control group. Both groups will receive standard care, including an individual lifestyle consultation in line with current national standards for preconception and early pregnancy. The intervention group will additionally attend three group sessions (online and physical) focused on health during preconception and early pregnancy, coping with stress and adherence to a healthy lifestyle. The advices are based on national guidelines for health during the preconception period and early pregnancy. Compliance with the prescribed advice is encouraged via newly developed digital platform

Interventions

  • Other Standard care
    Individual lifestyle consultation
  • Other Lifestyle program
    Lifestyle program focusing on lifestyle advice, coping with stress and adherence to a healthy(er) lifestyle. This program consists of 3 group sessions and an online platform.

Primary outcome measures

  • Preterm birth [Time frame: Assessed at birth]
  • Low birthweight/small-for-gestational-age [Time frame: Assessed at birth]
  • High birthweight/large-for-gestational-age [Time frame: Assessed at birth]
  • Low Apgar-score [Time frame: Assessed at birth]
  • Birth weight [Time frame: Assessed at birth]
Secondary outcome measures (12)
  • Adherence to lifestyle advice (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Sleep/wake rhythm (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Sleep/wake rhythm (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Social support (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Experience of stress (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Weight gain during pregnancy (mother) [Time frame: During pregnancy and early childhood, until 12 months]
  • Weight maintenance after 6 and 12 months pregnancy (mother) [Time frame: 12 months after birth of the child]
  • Time to pregnancy (mother) [Time frame: At delivery]
  • Occurrence of miscarriage (mother) [Time frame: At delivery]
  • Glucose metabolism and diabetes during pregnancy (mother) [Time frame: At delivery]
  • Occurrence of gestational hypertensive disorders during pregnancy (mother) [Time frame: At delivery]
  • Adherence to lifestyle advice (partner) [Time frame: During pregnancy and early childhood, until 12 months]

Eligibility criteria

Inclusion criteria

Women and their parents:

  • Planning a pregnancy or early pregnancy up to < 12 weeks
  • With the presence of at least one of the predetermined risk factors
  • Residential address in the municipality of Rotterdam and expected residential address in the municipality of Rotterdam at the birth of their child
  • Consent for participation

Exclusion criteria

Women and their partners:

  • Temporary or complete withdrawal from participation
  • Gestational age > 12+0 at study entry

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Netherlands · 1 center
  • Erasmus MC — Rotterdam

Identifiers

NCT: NCT05870878 · MEC-2022-0440, NL81446.078.22

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗