Impact of a Mobile Health Breastfeeding Counseling Intervention for Employed Mothers in Kenya

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWheaton College

About this trial

Exclusive breastfeeding (EBF) is critical for child survival, growth, and maternal health; however, over half of mothers in low and middle-income countries (LMIC). Mobile health (mHealth) describes a range of wireless technologies and techniques that seek to increase patient access to and interaction with preventive health services. This study will develop and test the feasibility of an mHealth intervention to improve support counseling for breastfeeding at a large sub-county referral hospital in Naivasha, Kenya.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Mothers over 18 years who are employed in contract-based labor in sectors that include education, business, healthcare, commercial agriculture, tourism/food service.

Mothers must reside in the greater Naivasha, Kenya area and receive maternal and child health care at the Naivasha sub-County Referral Hospital.

Disqualifiers

Mothers of infants with cleft deformities or other abnormalities that interfere with breastfeeding.

Trial design

Design model

Parallel

Treatments tested in this trial

  • mobile Health Breastfeeding Counseling

    Behavioral

    a phone-based breastfeeding counseling intervention, delivered by labor and delivery nurses, nutritionists, and maternal and child health nurses.

  • Standard of care breastfeeding counseling

    Behavioral

    The ongoing antenatal, delivery and postnatal breastfeeding and lactation counseling that is provided by the Naivasha sub-County Referral Hospital.

Treatment groups

284 Participants
are divided into 2 treatment groups
Group A: Standard of CareActive comparator 1 intervention
Group B: mobile Health (mHealth)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Exclusive breastfeeding at 24 weeks

The proportion of mothers who feed only breastmilk to their infants, without other liquids, formula or semi-solid or solid food.

Time frame
24 weeks post-partum

Secondary outcomes

1

Continued breastfeeding

Any breastfeeding in the past 24 hours

Time frame
36 weeks post partum
2

Early initiation of breastfeeding

Breastfeeding within 1 hour of childbirth

Time frame
Within 1 hour of childbirth

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Wheaton College

Lead sponsor

Kenya Medical Research Institute

Collaborator

This trial is not recruiting at the moment. You can still explore other options: