Impact of Maternal Stress on Infant Stunting

Sponsor
McGill University (Other)
Overall Status
Completed
CT.gov ID
NCT02755012
Collaborator
Center for Studies of Sensory Impairment, Aging and Metabolism (Other)
271
17

Study Details

Study Description

Brief Summary

This study takes place in rural Mam-Mayan communities of Guatemala characterized by high rates of childhood stunting. It aims to characterize women's exposure to nutrition, infection and psychosocial stressors vs. resilience factors, to evaluate the cumulative impact of maternal-level factors (nutritional, infectious, psychosocial), social factors (autonomy, social support, domestic violence), and household factors (socioeconomic status, food security) on early infant growth, and to evaluate whether maternal cortisol may be a mediator in the vertical transmission of stress.

Detailed Description

Grounded in participatory action research and a socio-ecological framework, this mixed-methods, observational study enrolled a longitudinal cohort of 155 women, seen during pregnancy (6-9 mo), early (0-6 wks) and later (4-6 mo) postpartum, and two cross-sectional cohorts (60 early, 56 later postpartum).

Maternal and infant anthropometry was recorded, maternal fecal, urine and saliva samples were collected, and questionnaires were used to explore household factors (socioeconomic status, food security), social factors (autonomy, paternal/social support, domestic violence), and maternal-level factors (nutrition, infection, emotional distress).

Analyses focused on (1) characterizing women's exposure to nutrition, infection and psychosocial stressors vs. resilience factors, (2) describing the maternal diurnal salivary cortisol rhythm in pregnancy and postpartum and explore its association with psychosocial variables, (3) assessing the cumulative impact of maternal-level factors (nutritional, infectious, psychosocial), social factors (autonomy, social support, domestic violence), and household factors (socioeconomic status, food security) on early infant growth, and (4) evaluating whether maternal cortisol may be a mediator in the vertical transmission of stress.

In addition, Photovoice activities involved giving a camera to 23 women from study communities, who documented sources of stress vs. resilience for local women, and shared photo-elicited narratives through six group sessions.

Study Design

Study Type:
Observational
Actual Enrollment :
271 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Reducing Maternal Stress Due to Infection, Malnutrition and Psychosocial Conditions of Poverty: A New Paradigm for Tackling Infant Stunting
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Nov 1, 2013
Actual Study Completion Date :
Nov 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Longitudinal

155 women enrolled in 2nd or 3rd trimester of pregnancy, and seen again, with their infant, at 0-6 wk postpartum, and 4-6 mo postpartum

Early Postpartum

60 women enrolled at 0-6 wk postpartum and seen once with their infant (cross-sectional)

Later Postpartum

56 women enrolled at 0-6 wk postpartum and seen once with their infant (cross-sectional)

Outcome Measures

Primary Outcome Measures

  1. Infant stunting (Infant height-for-age score) [0-6 wk]

    Infant height-for-age score measured at 0-6 wk

  2. Infant stunting (Infant height-for-age score) [4-6 mo postpartum]

    Infant height-for-age score measured at 4-6 mo postpartum

  3. Change in infant HAZ per month [Change over time (between 0-6wk and 4-6mo)]

    Change in infant HAZ score between 1st (0-6 wk) and 2nd (4-6 mo) visits

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Woman from study communities

  • Either pregnant or 0-6 wk postpartum or 4-6 mo postpartum

  • Consenting to participate

Exclusion Criteria:
  • Twin pregnancy

  • Not consenting to participate

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • McGill University
  • Center for Studies of Sensory Impairment, Aging and Metabolism

Investigators

  • Principal Investigator: Anne Marie Chomat, MD, PhD, MPH, McGill University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Anne Marie Chomat, Postdoctoral Fellow, McGill University
ClinicalTrials.gov Identifier:
NCT02755012
Other Study ID Numbers:
  • A04-B01-12A
First Posted:
Apr 28, 2016
Last Update Posted:
Apr 28, 2016
Last Verified:
Apr 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Anne Marie Chomat, Postdoctoral Fellow, McGill University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 28, 2016