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Rajarata Pregnancy Cohort (RaPCo)
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Sample details

RaPCo investigated the factors underlying maternal mortality and morbidity in Sri Lanka. Between 1 July and 30 September 2019, the study invited all pregnant women registering in the National Maternal Care Programme (Coverage 100%) in the Anuradhapura district, the largest district in Sri Lanka. The recruitment was district representative and amounted to almost 90% of all pregnant women. At baseline, the study included over 3,300 participants. The recruited women were in the early stages of pregnancy (less than 12 weeks gestation) and permanently resident in the Anuradhapura district. After the baseline assessment, participants were followed up at 25-28 weeks, 36 weeks, and at childbirth. The children of the RaPCo participants were included in a separate linked neonatal cohort.

Study design
Cohort

Number of participants at first data collection

3,374 (pregnant women)

Age at first data collection

≥ 18 years (participants)

Participant year of birth

Varied (participants)

Participant sex
Female

Representative sample at baseline?
Pregnant women of Anuradhapura district which is a predominantly rural largest district in Sri Lanka

Sample features

Cohort
Community-based sample
Maternal morbidities
Pregnant people
Dataset details

Country

Sri Lanka

Year of first data collection

2019

Primary Institutions

Rajarata University of Sri Lanka (ශ්‍රී ලංකා රජරට විශ්වවිද්‍යාලය/இலங்கை ரஜரட்ட பல்கலைக்கழகம்)

Links

doi.org/10.1136/bmjgh-2023-012852

Funders

State Ministry of Higher Education (උසස් අධ්‍යාපන රාජ්‍ය අමාත්‍යාංශය, உயர் கல்வி இராஜாங்க அமைச்சு)

World Bank

Ongoing?
No

Data types collected

mentalHealthData
qualitativeData
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • Interviews or focus groups
  • Qualitative survey
Neuroimaging data collection
  • None
Linked or secondary data
  • None
Features

Engagement

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Anaemia
    Anthropometry
    Biological samples/biospecimens
    Health determinants
    Health expenditure
    Healthcare access and use
    Human development
    Liver disease
    Maternal mental health
    Metabolic syndrome
    Out-of-pocket expenditure
    Pregnancy outcomes
    Social capital
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