- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06927674
DELIVER Evaluation in Nigeria
May 30, 2025 updated by: Valerie Flax, RTI International
Evaluation of the Global Alliance for Improved Nutrition (GAIN) DEcent LIVelihoods for Small-scale Producers Delivered Through Economic & Resilient Food Systems (DELIVER) Project in Nigeria
The DEcent LIVelihoods for small-scale producers delivered through Economic & Resilient food systems in Nigeria (DELIVER) (2024-2027) project is designed to address the low per capita consumption of vegetables and variety of vegetable consumption in northern Nigeria by working with smallholder farmers to increase production and promoting healthier diets through greater vegetable consumption among farmers and their neighbors.
The objective of this evaluation is to assess the effectiveness of GAIN's DELIVER program for increasing the quantity and variety of vegetables consumed by smallholder farmer households participating in the program and by neighbor households.
This evaluation will use a quasi-experimental design to assess the impact of GAIN's DELIVER programs on the quantity and diversity of vegetables consumed by smallholder farmers and non-farming neighbor households.
The evaluation will be guided by the RE-AIM (reach, effectiveness, adoption, implementation, maintenance) framework.
RE-AIM is a framework that is useful for evaluating the program impact of multifaceted and multilevel interventions.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
1568
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Valerie Flax, PhD, MPH
- Phone Number: (919) 541-6000
- Email: vflax@rti.org
Study Locations
-
-
-
Abuja, Nigeria
- Recruiting
- Datametrics Associates Ltd.
-
Principal Investigator:
- Valerie Flax, PhD, MPH
-
Principal Investigator:
- Rufina Ayogu
-
Principal Investigator:
- Moradeyo Otitoju
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Contact:
- Abiodun F. Ipadeola, PhD
- Phone Number: +234 806 447 0614
- Email: Abiodun.ipadeola@datametricsnigeria.com
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Principal Investigator:
- Abiodun F. Ipadeola, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Farmer household member or neighbor household recruited by DELIVER farmer
- Located within the intervention LGA
- Farmer must be a member who is participating in the DELIVER project
- Adult who is ≥ 18 years old
- Able to speak English or Hausa
- Provide informed consent to participate in the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Intervention
|
DELIVER is designed to address challenges of low consumption of vegetables in both variety and quantity by working with smallholder farmers to increase production and promoting healthier diets through greater vegetable consumption.
The project will build the capacity of smallholder farmers in vegetable production through collaborating with lead farmers to establish demonstration plots that showcase advanced agricultural techniques and technologies.
These plots will serve as training hubs for other farmers in vegetable production, postharvest handling, as well as business and market planning.
DELIVER aims to increase consumption among neighbors of the smallholder farmers by asking the farmers to recruit at least one neighbor family to whom they will regularly sell vegetables.
The project also includes a livelihood component that will increase market connections and access to finance for smallholder farmers.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantity of vegetables consumed
Time Frame: Baseline (April 2025), Endline (April 2027) (2 years)
|
Change in the mean grams of vegetables consumed in the previous 24 hours by farmer and neighbor households
|
Baseline (April 2025), Endline (April 2027) (2 years)
|
|
Variety of vegetables consumed
Time Frame: Baseline (April 2025), Endline (April 2027) (2 years)
|
Change in the number of types of vegetables consumed by farmer and non-farming neighbor households
|
Baseline (April 2025), Endline (April 2027) (2 years)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Abiodun F. Ipadeola, PhD, Datametrics Associates Ltd
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 12, 2025
Primary Completion (Estimated)
May 31, 2027
Study Completion (Estimated)
May 31, 2027
Study Registration Dates
First Submitted
April 7, 2025
First Submitted That Met QC Criteria
April 7, 2025
First Posted (Actual)
April 15, 2025
Study Record Updates
Last Update Posted (Actual)
June 4, 2025
Last Update Submitted That Met QC Criteria
May 30, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 424607
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Dataset will be shared through Nesstar.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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