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Neurological and Mental Health ConditionsMAMSNCT07432217

Mapping Antenatal Maternal Stress

An observational study of Neurological and Mental Health Conditions and Genetic Susceptibility, run by Institute for Human Development and Potential (IHDP), Singapore at 1 site in Singapore.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This study recruits women from early-mid pregnancy and later follows their children after birth, tracking both the mother and child until the child reaches at least 4 years of age. Read more about this study

Who is it for?
Ages 21 to 40 years, women onlyHealthy volunteers can take part
How many people
1,419 participants
Where
1 siteSingapore
Study dates
30 Sep 2019to 16 Jun 2029
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 40 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Study population: Singapore

Who may be able to join

  • Mothers aged 21 - 40 years
  • Below 24 weeks of pregnancy by ultrasonography
  • Proficient and able to respond to questionnaires in English
  • Intends for herself and her child to stay in Singapore for the next 5 years
  • Access to a smartphone or standard laptop/desktop
  • All participants whose data on pregnancy follow-up and delivery would be available from healthcare professionals
  • Willing to take part in this study and able to provide written consent

Who cannot join

  • Women with pre-existing or a history of psychotic depression, schizophrenia and bipolar disorders
  • Women currently on oral/IV steroids and/or thyroids medication
  • Women with a history of thyroid disease
  • Women who are pregnant via any assisted reproduction
  • Women carrying multiples
  • Women currently enrolled into any interventional randomized controlled trials

Trial locations and contacts

1 site in 1 country.

Singapore1 site
  • Institute for Human Development and Potential

    Singapore, 117609

Other trials in Singapore

About this study

Official title: Mapping Antenatal Maternal Stress (MAMS)

This study recruits women from early-mid pregnancy and later follows their children after birth, tracking both the mother and child until the child reaches at least 4 years of age. The study aims to examine the determinants of maternal mental health during pregnancy and how genetic factors could influence maternal mental health and child outcomes.

Read the detailed description

Prenatal maternal mental health has a significant long-lasting impact on both maternal functioning and child development. In Singapore and other developed nations, approximately 40% of pregnant women report symptoms of depression or anxiety at levels that predict poor maternal psychosocial functioning, as well as altered neurodevelopment and emotional-cognitive difficulties in their children. Despite the high prevalence and well-established consequences of prenatal mood disorders, the biological mechanisms underlying these conditions remain poorly understood. Prior research has implicated stress hormones, gonadal steroids, and genes, particularly within the serotonergic system, in contributing to perinatal depression and anxiety. However, candidate gene approaches have limitations. Mental health disorders arise from the combined effects of multiple genetic variants across distributed networks, rather than isolated loci. This understanding has led to the use of polygenic risk scores (PRS), which aggregate genetic variants associated with psychiatric conditions, to capture cumulative biological susceptibility. This MAMS study aims to build a predictive model for maternal antenatal i) anxiety, ii) depression, as well as iii) identify the genomic contribution to a composite score representing maternal mental health/well-being across a series of instruments. The research will also examine predictors of co-morbid conditions, notably depression and anxiety, where the effects on child developmental outcomes appear to be greater. Participants will be followed up from pregnancy through the child turning at least four years old. A subset of participants is enrolled in a sub-study Mapping Antenatal Maternal Stress - Child Outcomes (MAMS-CO).

Data will be collected through questionnaires done online, biological samples collection, and assessments done during lab-based visits.

  • Questionnaires related to depression, anxiety, psychosocial risk factors such as life stressors, social and partner support, socioeconomic factors, medical history, behavior, cognition, lifestyle, health status, parental bonding, childhood adversity experienced, socio-emotional factors, executive function, family dynamics, sleep quality, personality traits
  • Collection of samples such as blood, buccal swabs, and saliva
  • Sleep actigraphy measures on pregnant mothers and infants
  • Child developmental assessments
Keywords
Neurodevelopment, Genetics, Mental Health
Medical subject headings
Neurologic Manifestations, Genetic Predisposition to Disease, Psychological Well-Being

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07432217
Study groupRoleWhat they receive
Pregnant mothers, infants and childrenMothers who are aged 21 - 40 years, below 24 weeks of pregnancy by ultrasonography, are willing to respond to questionnaires in English, and intend to stay in Singapore with her child for the next 5 years are eligible for the study. Babies born from these mothers will be followed up until the child is at least 4 years old.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cumulative psychosocial risk index of maternal depression and anxiety

    To create a cumulative risk index by collecting data using existing validated measures on known risk factors for maternal depression and anxiety, including 1) low socio-economic status, 2) poor marital relations, 3) low social support, 4) high levels of perceived stress, 5) high levels of neuroticism, 6) low self-esteem, 7) poor family function, and 8) childhood adversity in the form of maltreatment and/or poor parental relations.

    Measured: From pregnancy up to 2 years postnatal

  2. Polygenic risk score for differential susceptibility to environmental susceptibility

    To identify genotypic variation associated with perinatal maternal mental health

    Measured: From pregnancy up to 2 years postnatal

  3. Determinants of maternal symptoms of depression and anxiety with those that predict positive maternal mental health

    To compare the determinants of maternal symptoms of depression and anxiety with those that predict the level of positive mental health

    Measured: From pregnancy up to 2 years postnatal

Secondary outcomes (3)
  1. Influence of perinatal maternal mental health in relation to child development outcomes

    To examine the impact of perinatal maternal mental health on child development outcomes using standardized clinical measures that have predictive validity for cognitive, emotional and social outcomes in young children. Our analyses will feature candidate moderators of the association between maternal mental health and child outcomes, including socioeconomic status, family cohesion and parental attitudes. We will also examine the moderating influence of the polygenic risk scores in determining the strength of the association between maternal mental health and specific child cognitive - emotional outcomes.

    Measured: From pregnancy to postnatal 6 years

  2. Determine specific contribution of maternal prenatal mood factor components to specific developmental outcomes in children

    Analyses of maternal prenatal mood factors (e.g., maternal positive mental health, somatic complaints, anxiety, etc.) to determine which components contribute to specific developmental outcomes in children.

    Measured: From pregnancy to postnatal 6 years

  3. Influence of genetic susceptibility on maternal mental health and child outcomes

    Exploratory analysis of the hypothesized moderating effect of the polygenic risk scores to examine those SNP's that best account for the association between the psychosocial risk index, maternal mental health and child outcomes.

    Measured: From pregnancy to postnatal 6 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Feb 2026
  2. Study start30 Sep 2019
  3. Primary completionJun 2029 (estimated)
  4. Study completion16 Jun 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,419 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07432217
Sponsor's protocol ID
2018/00967
Other IDs
2018
Acronym
MAMS
Status last verified
Feb 2026
First submitted
12 Feb 2026
Last updated
25 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Neurological and Mental Health Conditions and Genetic Susceptibility, run by Institute for Human Development and Potential (IHDP), Singapore at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 25 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cumulative psychosocial risk index of maternal depression and anxiety (time frame: From pregnancy up to 2 years postnatal). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Feb 2026.

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