Actively Recruiting

Phase Not Applicable
Age: 1Day - 59Months
All Genders
Healthy Volunteers
NCT06025786

Impact Evaluation of Benazir Nashonuma Program (BNP) on Stunting Among Under-five Children

Led by Aga Khan University · Updated on 2023-09-11

13200

Participants Needed

1

Research Sites

238 weeks

Total Duration

On this page

Sponsors

A

Aga Khan University

Lead Sponsor

I

International Food Policy Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of the study is to evaluate the impact of Benazir Nashonuma Program (BNP) on prevalence of stunting among under-five children in low income setting of Pakistan. The research question that the study aims to answer is: Is there any change in the prevalence of stunting among under-five children in districts where Benazir Nashonuma Program (BNP) is established compared to districts where BNP is not established? Districts where BNP is functional, and women and children are receiving the intervention will be compared at baseline and end line with control districts where conventional reproductive care services are given. Prevalence of stunting among under-five children will be compared along with other nutritional and growth status indicators over a period of 4 years.

CONDITIONS

Official Title

Impact Evaluation of Benazir Nashonuma Program (BNP) on Stunting Among Under-five Children

Who Can Participate

Age: 1Day - 59Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Households with an under-five child whose mother is registered with the Benazir Income Support Program (BISP)
  • Both the child and mother are available at the time of interview
Not Eligible

You will not qualify if you...

  • Child's mother is younger than 15 years or older than 49 years

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Trial Site Locations

Total: 1 location

1

Aga Khan University

Karachi, Sindh, Pakistan, 75290

Actively Recruiting

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Research Team

S

Sajid Bashir Soofi, MD, CPSP

CONTACT

S

Shah Muhammad, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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