Skip to main content
OpenTrials
Completed

NCT Number: NCT05389540

Rural South and Southeast Asia Household Health Survey

A cross-sectional household survey with two-stage cluster-randomized sampling. This cross-sectional household survey design to recruit a random sample of households that is representative for each of the study sites. From the selected households, all consenting, household members will be included in the study.

This study is funded by the UK Wellcome Trust. The grant reference number is 215604/Z/19/Z

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

BangladeshBuilding Resources Across Communities (BRAC), Dhaka, Bangladesh

Loading trial locations.

About this study

371 households will be randomly selected from each site in Bangladesh, Cambodia, Myanmar, and Thailand. Assuming each household has an average of 4.5 members and all members will be sampled, 1500 participants will be recruited per site. This sample size allows for the overall prevalence estimation of key survey indicators with 95% confidence and 5% degree of precision.

The survey components include questionnaire interview, physical examination, blood sample collection, and point of care (PoC) tests. The questionnaire interview will collect information on household characteristics, members' disability, presence or history of disease, risk factors, self-perceived quality of life, and health seeking behaviour. For women, questions about reproductive health and antenatal care, and for young children, vaccination coverage and achievement of child development goals, will also be assessed.

For physical examinations, tympanic temperature, weight and height will be measured in all household members, mid-upper arm circumference in young children, and blood pressure in adults. Blood sample will be collected from all participants aged 6 months and above. Venous blood samples will be collected from participants aged 5 years and older, and dried blood spot will be collected from children under 5 years. Samples will be shipped to a central laboratory and analysed. Haemoglobin PoC will be administered to all participants.

All data will be collected directly on an electronic case report form using tablets, and uploaded to an electronic database.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • All members of the selected households at the time of the survey; and able to provide informed consent.

Exclusion criteria

  • Adults or children whose parent/guardian/ caretaker are unable or unwilling to provide informed consent.

Treatment and study plan

Primary outcomes

  1. Prevalence of long-lasting antibodies (IgG) against selected causes of non-malaria febrile illnesses

    Time frame: Upon enrollment

  2. Prevalence of Plasmodium spp. by PCR

    Time frame: Upon enrollment

  3. Prevalence of chronic Hepatitis B and C

    Time frame: Upon enrollment

  4. Prevalence of selected non-communicable diseases (e.g. diabetes, chronic obstructive pulmonary diseases, stroke) according to self-reported disease history and laboratory tests

    Time frame: Upon enrollment

  5. Prevalence of reported disability

    Time frame: Upon enrollment

  6. Lifetime prevalence of reported injury or death caused by an accident

    Time frame: Upon enrollment

  7. Self-rated overall health status

    Time frame: Upon enrollment

  8. Questionnaire evaluation of health-related quality of life

    Time frame: Upon enrollment

  9. Prevalence of self-reported tobacco, alcohol, and other substitute use among the population aged 15 and above

    Time frame: Upon enrollment

  10. Prevalence of underweight and overweight, raised blood pressure and total cholesterol

    Time frame: Upon enrollment

Secondary outcomes

  1. Evaluation of household wealth quartile according to self-reported household characteristics

    Time frame: Upon enrollment

  2. Education level, marital status, and occupation

    Time frame: Upon enrollment

  3. Self-reported health-related household characteristics (e.g. household cooking fuel, source of drinking water, possession of mosquito net)

    Time frame: Upon enrollment

  4. Proportion of population self-reported having sought for medical care in the past month, and care providers visited

    Time frame: Upon enrollment

  5. Self-reported antenatal care coverage among women who have ever given birth

    Time frame: Upon enrollment

  6. Reported vaccination coverage among children < 3 years

    Time frame: Upon enrollment

  7. Prevalence of reported exclusive breast feeding among children < 5 years

    Time frame: Upon enrollment

  8. Prevalence of children aged 3-4 years who have reached early child development milestones, reported by caretaker

    Time frame: Upon enrollment

  9. Presence of self-reported symptoms or diagnosed illness besides the outcome measures of the primary objectives

    Time frame: Upon enrollment

  10. Reported illness in the last month and type of illness

    Time frame: Upon enrollment

  11. Prevalence of IgM antibodies against selected acute non-malaria causes of febrile illness

    Time frame: Upon enrollment

Sponsors and collaborators

Lead sponsor

University of Oxford

Other

Collaborators

  • Bangladesh Rural Advancement Committee
  • Cambodia Action for Health Development (AHEAD)
  • Chiang Rai Clinical Research Unit, Thailand
  • Mahidol Oxford Tropical Medicine Research Unit
  • Myanmar Oxford Clinical Research Unit

Registry information

Official study title

Overview of Disease Burden in Rural South and Southeast Asia: A Cross-sectional Household Health Survey With Questionnaire Interviews and Selected Laboratory Tests

Acronym: SEACTN-HHS

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
May 25, 2022
Registry last updated
Feb 28, 2024

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.