Promotion of Exclusive Breast Feeding and Young Child Feeding Practices Through m-Health

Sponsor
Aga Khan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05590351
Collaborator
(none)
258
1
2
24
10.7

Study Details

Study Description

Brief Summary

Early life nutrition is the key modifiable determinant of child growth, development, survival and diseases of adult onset. Pakistan ranks highest for neonatal mortality rate (44.2/1000 live births (LBs)) globally. One third of under-five deaths (74.9/1000 LBs) are attributable to high prevalence of stunting (38%), underweight (23%) and wasting (7%), greatly related to feeding practices. Given the low prevalence of exclusively breast fed (EBF) (48%) and use of minimum acceptable diet (13%), mitigation of early life nutritional risk through promotion of EBF and Young Child Feeding Practices (YCFP) provides a critical window of opportunity for intervention. Secondary Care Hospitals (SCH) of the Aga Khan Health Services Pakistan provide essential maternal and child health services for low-middle income population. Babies born at these SCHs are followed up for vaccination, growth-monitoring and other services at the closely affiliated Family Health Centers (FHCs) run by Lady Health Visitors (LHVs). We aim to examine the effectiveness of a locally designed m-Health application for empowering mothers for child nutritional care as a potentially sustainable approach. The first six months of formative research would identify perceptions, barriers and facilitators for EBF and YCFP using self-determination behavioral theory, among multi-parous pregnant mothers enrolled at three SCHs of Karachi. A randomization trial would be conducted during next 18 months among near-term pregnant women who have access to smart-phones. A culturally appropriate mhealth application called first diet would be developed to provide personalized push messages delivered weekly by the LHVs. Non-intervention group will receive face-face nutritional counselling by the research staff at FHC following routine vaccination and growth-monitoring schedule. Mothers would followed-up from one month prior to expected delivery to child's first birthday. We expect 20% improvement in rates of EBF and YCFP with m-Health intervention. If proven effective, m-health would be incorporated in routine child care provision by LHVs.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: First diet: m-health coaching application
  • Behavioral: Face to Face counselling
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
258 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
m-health coaching applicationm-health coaching application
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Promotion of Exclusive Breast Feeding and Young Child Feeding Practices Through m-Health: A Randomized Controlled Trial
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

m-health coaching application

Behavioral: First diet: m-health coaching application
Intervention for the study would comprise of a culturally appropriate m-health application called first diet. This application will be developed considering the perceptions, barriers and facilitators identified through formative research. Content of the messages would focus on breastfeeding, its importance and early initiation within one hour of birth, significance of first feed i.e. colostrum, importance of EBF from birth till 6 months, introduction of complementary feeding to 6-8 months old infants and appropriate YCFP. These messages would be drafted in the local preferable language assessed during formative research. The content of the messages would be translated and then back translated to ensure validity. These messages will be short, contextual and tailored according to the women's stage of gestation, delivery and infant's age

Active Comparator: Standard of care

Face to face counselling

Behavioral: Face to Face counselling
Women randomly enrolled in the non-interventional group will receive face-face nutritional counseling instead of mobile application. Once enrolled in the group, Research Assistant (RA) will collect relevant details on the baseline questionnaire like intervention group but on a paper-based questionnaire. Women will be given first face-face counseling on the day of enrollment. The counseling sessions will coincide with the routine vaccination and growth monitoring schedule of the infant after women deliver

Outcome Measures

Primary Outcome Measures

  1. Early Initiation of Breastfeeding (EIBF) [1 year]

    EIBF is defined as the proportion of children put to the breast within one hour of birth

  2. Exclusive Breast Feeding (EBF) [1 year]

    EBF up to 6 months of age defined as proportion of infants of 0-6 months of age who are fed exclusively with breast milk

  3. Introduction of solid, semi-solid or soft foods [1 year]

    Introduction of solid, semi-solid or soft foods defined as the proportion of infants 6-8 months of age who receive solid, semi-solid or soft foods.

  4. Minimum dietary diversity [1 year]

    Minimum dietary diversity is defined as the proportion of children 6-12 months of age who receive food from 4 or more food groups

  5. Meal frequency [1 year]

    Meal frequency defined as the average number of daily meals for children 6-12 months of age, who receive solid, semi-solid, or soft foods Infant and young child feeding indicator

  6. Minimum acceptable diet [1 year]

    Minimum acceptable diet is a composite variable and would be based on meal frequency and dietary diversity.

  7. Mean Duration of BF [1 year]

    Mean Duration of BF defined as average duration an infant is breastfed for 12 months.

  8. Continued BF at 1 year [1 year]

    Continued BF at 1 year defined as the proportion of children 12 months of age who are still on breast milk.

Secondary Outcome Measures

  1. Acute respiratory Infection (ARI) [1 year]

    Acute respiratory Infection will be defined as short, rapid breathing that is chest-related and/or difficult breathing that is chest-related. Percentage of children up to 1 year of age with symptoms of ARI at any time in the last 2 weeks preceding the follow-up.

  2. Acute Diarrhea [1 Year]

    Acute Diarrhea will be defined as the passage of three or more loose or liquid stools per day (or more frequent passage than is normal for the individual). The frequent passing of formed stools is not diarrhea, nor is the passing of loose, "pasty" stools by breastfed babies. Percentage of children up to 1 year of age with symptoms of diarrhea at any time in the last 2 weeks preceding the follow-up.

  3. Visit to the Emergency room [1 year]

    Visit to the Emergency room will be defined as the infant brought to the emergency room for management of any acute illness in the past 2 weeks.

  4. Hospitalization [1 year]

    Hospitalization will be defined as the infant admitted to the hospital for diagnosis or management of any acute illness in the past 2 weeks.

  5. Stunting (height-for-age) [1 year]

    Stunting will be defined as Children whose height-for-age Z-score is below minus two standards deviations (-2 SD) from the median of the reference population

  6. Severe stunting [1 year]

    Children who are below minus three standard deviations (-3 SD) are considered severely stunted

  7. Wasting (weight-for-height) [1 year]

    Wasting will be defined as the children whose Z-score is below (-2 SD) from the median of the reference populations are considered thin (wasted), or acutely undernourished

  8. Severely wasted [1 year]

    Children whose weight-for-height Z-score is below minus three standards deviations (-3 SD) from the median of the reference population are considered severely wasted

  9. Overweight (weight-for-height) [1 year]

    Children whose weight-for-height Z-score is more than 2 standard deviations (+2 SD) above the median of the reference population is considered overweight.

  10. Underweight (weight-for-age) [1 year]

    Children whose weight-for-age Z-score is below (-2 SD) from the median of the reference population are classified as underweight.

  11. Severely underweight [1 year]

    Children whose weight-for-age Z-score is below minus three standards deviations (-3 SD) from the median are considered severely underweight.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Hour to 1 Year
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Pregnant women in the third trimester at 36 +/- 1 week of gestation.

  2. Planned to stay in their respective areas for at least 1 year after delivery

  3. Planned to get the infant immunized from the respective FHC of the hospitals.

  4. Have access to smart phones with internet connection.

  5. Registered and planning to deliver to any of the Secondary Care Hospitals

  6. Can read and write in local language (English and/or Urdu).

  7. Consent to participate and remain in the study until 1 year of child age

Exclusion Criteria:
  1. Women who do not possess smart phone.

  2. Women who plan to move to different location after delivery.

  3. Women with complicated pregnancy that might require referral by the end of pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Aga Khan University Karachi Sindh Pakistan 74000

Sponsors and Collaborators

  • Aga Khan University

Investigators

  • Principal Investigator: Rozina Nuruddin, PhD, Agha Khan University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Rozina Nuruddin, Assistant Professor, Aga Khan University
ClinicalTrials.gov Identifier:
NCT05590351
Other Study ID Numbers:
  • 2022-3424-20757
First Posted:
Oct 21, 2022
Last Update Posted:
Oct 21, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rozina Nuruddin, Assistant Professor, Aga Khan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 21, 2022