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Clinical Trials/ISRCTN17842200
ISRCTN17842200
Completed
N/A

Virtual Antenatal Intervention for improved Diet and Iron intake (VALID): A randomized controlled trial in Kapilbastu district, Nepal

HERD International0 sites319 target enrollmentJanuary 13, 2022
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ConditionsPrevention of iron deficiency anaemia during pregnancyPregnancy and Childbirth

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prevention of iron deficiency anaemia during pregnancy
Sponsor
HERD International
Enrollment
319
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/36797013/ (added 17/02/2023) 2023 Other publications in https://doi.org/10.1186/s12889-023-16195-5 Process evaluation (added 01/08/2023) 2023 Preprint results in https://dx.doi.org/10.2139/ssrn.4527762 (added 15/02/2024)

Registry
who.int
Start Date
January 13, 2022
End Date
December 31, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
HERD International

Eligibility Criteria

Inclusion Criteria

  • •1\. Pregnant girl/woman aged between 13 to 49 years
  • •2\. Able to respond to questions
  • •3\. Resident of study cluster (whether at husband’s or parental home)
  • •4\. Less than or equal to 28 weeks’ gestation estimated from recall of last menstrual period (or expected date of delivery given by a health worker)
  • •5\. Plans not to leave the country during the follow\-up period 5 weeks since enrolment
  • •6\. Does not have another pregnant woman in her household already enrolled in the trial
  • •7\. Consents to participate in the trial

Exclusion Criteria

  • •1\. Aged \<\=12 years or \>\=50 years
  • •2\. Not\-consenting to participate in the trial
  • •3\. Unable to respond to questions
  • •4\. \=28 weeks’ gestation at enrolment as estimated from LMP (or expected date of delivery given by a health worker)
  • •5\. Planning to leave the country during follow up period.
  • •6\. Has another pregnant woman in her household already enrolled in the trial

Outcomes

Primary Outcomes

Not specified

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