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Effectiveness of an HIV-adapted IMCI Training and Supervision Programme for Community Health Workers

U

University of KwaZulu-Natal (UKZN)

Status

Completed

Conditions

Infant Feeding Practices
Postnatal Health Care Utilization
Antenatal Health Care Utilization
Prevention of Mother-to-child Transmission of HIV

Treatments

Behavioral: Enhanced HIV and MCH training for CHW

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT01774136
Nompilo

Details and patient eligibility

About

This is a cluster randomized controlled trial (C-RCT) to evaluate the effectiveness of a Community-Integrated Management of Childhood Illness (C-IMCI) training for community caregivers (CCGs), adapted to include HIV-related interventions, on the delivery of maternal, newborn and child health interventions within households in rural communities in Ugu District, KwaZulu-Natal (KZN) Province, South Africa. The intervention includes two components: (1) a 2-week HIV/C-IMCI training for CCGs and their associated facilitators and supervisors, and (2) continuous support and supervision following the continuous quality improvement (CQI) framework, a low-technology approach to management and supervision of health programs. The primary objectives of the proposed evaluation are to measure the effect of the intervention on key outcomes, including early uptake of antenatal care, facility based delivery, postnatal visits, coverage of exclusive breastfeeding, and uptake of HIV PCR testing in infants at 6 weeks. We will also examine the effects of the intervention on immunization uptake up to 12 months and knowledge and practices of CCGs and mothers pertaining to maternal, newborn and child health.

Enrollment

1,342 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Community caregivers

  • CCGs who work in Ugu District
  • age 18 years or older
  • with grade 9 education or greater

Mothers

  • Mothers age 18 years and older who delivered a live-born infant within the prior 12 months
  • Reside in households served by participating CCGs.

Exclusion criteria

  • None

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1,342 participants in 2 patient groups

Enhanced HIV and MCH training for CHW
Experimental group
Description:
The intervention includes two components: (1) a 2-week HIV/C-IMCI training for CCGs and their associated facilitators and supervisors, and (2) continuous support and supervision following the continuous quality improvement (CQI) framework, a low-technology approach to management and supervision of health programs.
Treatment:
Behavioral: Enhanced HIV and MCH training for CHW
Standard of Care
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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