ClinicalTrials.Veeva

Menu

Assessing Cost and Effectiveness of Training and Supervision of Front Line Workers on Early Breastfeeding Practices (iycfch)

E

Eminence

Status and phase

Completed
Phase 1

Conditions

Malnutrition

Treatments

Behavioral: Improve Early Breastfeeding

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01407224
09-000076-AT10,EMI

Details and patient eligibility

About

The aim of this operational research is to compare the cost-effectiveness of two methods for capacity building of existing TBAs/CVs to improve rates of delayed cord clamping, early skin to skin contact and infant-led initiation of breastfeeding, to reduce prelacteal feeding and increase early exclusive breastfeeding in research areas of rural Bangladesh.

Full description

Suboptimal early infant feeding practices are the norm in Bangladesh, and contribute to its poor infant health and nutrition. However, the modern health services are unable to help because approximately 85% of births take place at home. The Government has begun the huge process of training the informal community traditional birth attendants (TBAs) who, along with community volunteers (CVs), deliver the majority of babies, especially in the rural areas. The proposed operations research will take place in one of the poorest rural districts. It will compare the cost effectiveness of practical training of these relatively uneducated community members, with or without supportive supervision in improving early infant feeding practices, using a cluster-randomized study design. The practices to be measured before and after on probability samples include: 1) delayed cord clamping, 2) early skin to skin contact and 3) newborn-led initiation of breastfeeding within one hour of birth, 4) avoidance of the traditional prelacteal feeds, and 5) exclusive breastfeeding, at least for the early months. Costs will be carefully monitored so as to compare the cost per behavior improved per infant.

Enrollment

1,200 patients

Sex

All

Ages

1 day to 5 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Lactating women of children ages 0 to 5 months and pregnant women with second and third trimester

Exclusion criteria

  • First trimester women and lactating women of children ages 6 to 23 months.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1,200 participants in 3 patient groups

Only training
Experimental group
Description:
Training on Early Breastfeeding Practices to front line health workers
Treatment:
Behavioral: Improve Early Breastfeeding
Training and supervision
Active Comparator group
Description:
Training as well as supervision by field supervisor for six months intervention
Treatment:
Behavioral: Improve Early Breastfeeding
Control
No Intervention group
Description:
No intervention such as training or supervision
Treatment:
Behavioral: Improve Early Breastfeeding

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems