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GrowthEHFPNCT01825226

Helen Keller International's Enhanced-Homestead Food Production Program in Burkina Faso

A study testing Enhanced-Homestead Food Production Program in people with Growth and Anemia, run by International Food Policy Research Institute at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Helen Keller International (HKI) has been implementing homestead food production (HFP) programs in Asia for the past 20 years and has recently begun implementing HFP programs in Africa as well. Read more about this study

Who is it for?
Ages 3 to 12 months
Conditions the study is for
Growth, Anemia
What is being tested?
Enhanced-Homestead Food Production Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,763 participants
Where
1 siteUnited States
Study dates
Feb 2010to 28 Sep 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 12 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Mother of child between the ages of 3 and 12 months and her child

Who cannot join

  • N/A

Trial locations and contacts

1 site in 1 country.

United States1 site
  • International Food Policy Research Institute

    Washington D.C., District of Columbia, 20006

Other trials in United States

About this study

Official title: THE IMPACT OF THE ENHANCED HOMESTEAD FOOD PRODUCTION PROGRAM ON CHILD HEALTH

Helen Keller International (HKI) has been implementing homestead food production (HFP) programs in Asia for the past 20 years and has recently begun implementing HFP programs in Africa as well. In general, these programs target women and are designed to improve maternal and child health and nutrition outcomes through three primary pathways: 1. Increasing the availability of micronutrient-rich foods through increased household production of these foods; 2. Raising income through the sale of surplus production; and 3. Increasing knowledge and adoption of optimal nutrition practices, including the consumption of micronutrient-rich foods. Evaluations of HFP programs have consistently demonstrated significant increases in household production and consumption of micronutrient-rich foods. This increased consumption, along with improvements in health and nutrition related knowledge, and increased income, could all contribute to improvements in maternal and child health and nutrition outcomes. However, to date there has been limited understanding as to how these types of programs can be optimized to maximize impacts on these outcomes.

In order to better understand the potential of these types of programs to improve maternal and child health and nutrition outcomes and how this impact may be achieved IFPRI has been collaborating with HKI to evaluate one of their E-HFP programs in Burkina Faso. The evaluation considers impact of the program through the three pathways above, and assesses anthropometric and clinical measures of nutrition, as well as looking at how the programs might be improved.

Conditions
Growth, Anemia
Being tested
Enhanced-Homestead Food Production Program
Medical subject headings
Anemia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Enhanced-Homestead Food Production ProgramOther

    Participation in an enhanced-homestead food production program including home gardening and nutrition and health behavior change communication

Study groups in NCT01825226
Study groupRoleWhat they receive
Program participationExperimentalParticipation in an enhanced-homestead food production program including home gardening and nutrition and health behavior change communication
Receives: Other: Enhanced-Homestead Food Production Program
ControlNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Growth

    Change in height-for-age Z-scores, weight-for-age Z-scores and weight-for-height Z-scores will be measured as well as the change in the prevalence of stunting (HAZ <-2), underweight (WAZ <-2) and wasting (WHZ <-2) over the course of the two year program period.

    Measured: Measurements will be made for children between the ages of 3 and 12 months of age at baseline and then 2 years later, at endline, when the children are between the ages of 23 and 40 months

  2. Hemoglobin

    Measured: Measurements will be made for children between the ages of 3 and 12 months of age at baseline and then 2 years later, at endline, when the children are between the ages of 23 and 40 months

Secondary outcomes (8)
  1. Food security

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  2. Household assets

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  3. Household consumption

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  4. Household livestock holdings

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  5. Dietary diversity

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  6. Mother's BMI

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  7. Maternal health and nutrition-related knowledge

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

  8. IYCF practices

    Measured: Baseline (2010), Endline (2012), follow-up (2013)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Apr 2013 (estimated)
  2. Study startFeb 2010
  3. Primary completionJun 2013
  4. Study completion28 Sep 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
1,763 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01825226
Sponsor's protocol ID
6117001
Acronym
EHFP
Status last verified
Apr 2025
First submitted
1 Jan 2013
Last updated
1 May 2025
Results posted
No
Data monitoring committee
No

Publications

  • Nielsen JN, Olney DK, Ouedraogo M, Pedehombga A, Rouamba H, Yago-Wienne F. Process evaluation improves delivery of a nutrition-sensitive agriculture programme in Burkina Faso. Matern Child Nutr. 2018 Jul;14(3):e12573. doi: 10.1111/mcn.12573. Epub 2017 Dec 26.

    PubMed 29278449
  • Olney DK, Bliznashka L, Pedehombga A, Dillon A, Ruel MT, Heckert J. A 2-Year Integrated Agriculture and Nutrition Program Targeted to Mothers of Young Children in Burkina Faso Reduces Underweight among Mothers and Increases Their Empowerment: A Cluster-Randomized Controlled Trial. J Nutr. 2016 May;146(5):1109-17. doi: 10.3945/jn.115.224261. Epub 2016 Apr 13.

    PubMed 27075910
  • Olney DK, Pedehombga A, Ruel MT, Dillon A. A 2-year integrated agriculture and nutrition and health behavior change communication program targeted to women in Burkina Faso reduces anemia, wasting, and diarrhea in children 3-12.9 months of age at baseline: a cluster-randomized controlled trial. J Nutr. 2015 Jun;145(6):1317-24. doi: 10.3945/jn.114.203539. Epub 2015 Apr 22.

    PubMed 25904734

Questions about this trial

What is this clinical trial studying?

A study testing Enhanced-Homestead Food Production Program in people with Growth and Anemia, run by International Food Policy Research Institute at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Growth (time frame: Measurements will be made for children between the ages of 3 and 12 months of age at baseline and then 2 years later, at endline, when the children are between the ages of 23 and 40 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01825226, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2025.

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