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Completed

NCT Number: NCT02238704

Cornell University-Micronutrient Initiative Calcium Supplementation Study

The World Health Organization (WHO) now recommends prenatal calcium supplementation for prevention of preeclampsia in populations with inadequate dietary intake. This study seeks to compare the effect of two dosing strategies on the amount of supplement ingested by pregnant women and adherence to related recommendations.

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Key information

Age range

15 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Chebwayi Health centre, Kakamega, Kenya

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About this study

This study is a non-inferiority trial that compares the effect of a dosing strategy involving lower overall dose and fewer administrations per day to the current WHO recommendation. The comparator arm, Regimen B, prescribes 3 doses per day (consistent with current WHO standard) and was found to be burdensome in qualitative studies. The experimental arm, Regimen A, prescribes 2 doses per day and has been associated with greater satisfaction. On face value Regimen A should result in 33% less amount of supplement ingested than Regimen B. However, we hypothesize that the difference in amount ingested, when rolled out in routine practice will be MUCH LESS than that BECAUSE THE LOWER DOSE REGIMEN RESULTS IN HIGHER LEVELS OF ADHERENCE. We hypothesize that THE DIFFERENCE IN AMOUNT CONSUMED WILL BE NEGLIGIBLE OR will not exceed 15%. Hence, we hypothesize that Regimen A is not inferior to Regimen B in terms of total amount of supplement ingested (within a 15% margin of inferiority).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Attendance at ANC clinic in a primary care facility in Kakamega north

Exclusion criteria

  • Gestational age < 16 weeks,
  • Gestational age > 30 weeks,
  • Dietary or medicinal consumption of adequate calcium (according to the screening survey),
  • Intention to leave study community before 8weeks from date of interview

Treatment and study plan

Regimen A calcium and iron/folic acid

Dietary Supplement

Comparison of recommended administration schedule for calcium and iron/folic acid supplements in pregnant women

Regimen B calcium and iron/folic acid

Dietary Supplement

Comparison of recommended administration schedule for calcium and iron/folic acid supplements in pregnant women

Primary outcomes

  1. Amount of calcium supplement ingested

    Time frame: 8 weeks after ANC consultation, during which recruitment into the study occurred

    This is the actual number of supplements ingested expressed as a percentage of the number of supplements expected to be ingested since the ANC consultation if 100% adherent to the current WHO recommendation.

    [Total number of calcium supplements consumed/(Number of days since last ANC consultation X 3)] X 100

Secondary outcomes

  1. Adherence to related recommendations

    Time frame: 8 weeks after ANC consultation, during which recruitment into the study occurred

    Adherence to other features of the WHO recommendation (taking supplements with food).

  2. Motivation

    Time frame: 8 weeks after ANC consultation, during which recruitment into the study occurred

    Motivation scores extracted from the survey instrument administered at follow up.

  3. Self-efficacy

    Time frame: 8 weeks after ANC consultation, during which recruitment into the study occurred

    Self-efficacy scores extracted from the survey instrument administered at follow up.

  4. Satisfaction

    Time frame: 8 weeks after ANC consultation, during which recruitment into the study occurred

    Satisfaction scores extracted from the survey instrument administered at follow up.

Sponsors and collaborators

Lead sponsor

Cornell University

Other

Collaborators

  • Kenya Ministry of Health
  • Micronutrient Initiative
  • University of Nairobi

Registry information

Official study title

A Cluster-randomized, Non-inferiority Open-label Trial of the Impact of Supplementation Regimen on Consumption of Prenatal Calcium and Iron/Folic Acid Supplements and Adherence to Related Recommendations

Acronym: MICA

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Sep 12, 2014
Registry last updated
Jul 27, 2016

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.

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