search
Back to results

Supplementation Trial of KOKO Plus Among HIV Exposed Children in Accra

Primary Purpose

HIV Infections, Nutrition Poor, Child Development

Status
Unknown status
Phase
Not Applicable
Locations
Ghana
Study Type
Interventional
Intervention
KOKOPlus protein and micronutrient powder
Sponsored by
Noguchi Memorial Institute for Medical Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring HIV-Exposed, Nutrient Status, KOKOPlus

Eligibility Criteria

6 Months - 18 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Mother-infant dyads; HIV positive mothers and children between 6 and 12 months of age attending antiretroviral (ART) Clinics and child HIV Clinics.

Exclusion Criteria:

  • Mothers who decline to participate in the study

Children with severe acute malnutrition (mid-upper arm circumference <115 mm or a weight-for-height/length <-3 Z-scores of the WHO growth standards).

Children on hospital admission

Children with diagnosed or apparent congenital conditions such as encephalitis, cleft palate, hole in heart, which negatively affect the child's ability to eat and/or growth.

Sites / Locations

  • 37 Military HospitalRecruiting
  • Greater Accra Regional HospitalRecruiting
  • Korle-bu Teaching HospitalRecruiting
  • Princess Marie Louise Children's HospitalRecruiting
  • Ashaiman PolyclinicRecruiting
  • Tema General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

KOKOPlus protein and micronutrient powder , a complementary food supplement containing soya powder, sugar and oil along with the essential amino acid lysine and a micronutrient mix was formulated. Two weeks' supply of KOKOPlus sachets will be given to intervention arm participants every fortnight for 6 months to be mixed into any cereal, soup, stew, or other food given to the children.

This arm will receive no supplement and no placebo for the duration of the study.,

Outcomes

Primary Outcome Measures

Anthropometry
Length-for-age Z score, Weight-for-age Z score. Weight for length Z score
Haemoglobin
(g/dl), anaemia
Child developmental Milestones achieved

Secondary Outcome Measures

Morbidity
Incidence of fever, malaise, loss of appetite

Full Information

First Posted
August 6, 2021
Last Updated
November 5, 2021
Sponsor
Noguchi Memorial Institute for Medical Research
Collaborators
International Food Policy Research Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT04995874
Brief Title
Supplementation Trial of KOKO Plus Among HIV Exposed Children in Accra
Official Title
Supplementation Trial of KOKO Plus Among HIV Exposed Children in Accra
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 6, 2021 (Actual)
Primary Completion Date
June 25, 2022 (Anticipated)
Study Completion Date
June 25, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Noguchi Memorial Institute for Medical Research
Collaborators
International Food Policy Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall aim of the research is to conduct a randomised controlled trial of KOKOPlus in young HIV exposed children attending HIV clinics in Accra, Ghana to test the effectiveness of KOKOPlus over a period of 6 months to improve nutritional status and child development in HIV exposed children 6-18 months of age in Accra
Detailed Description
The specific objectives are to accomplish the following To test the effectiveness of KOKOPlus to improve the nutritional status of HIV exposed infants aged 6-18 months. To measure and compare nutritional status in intervention and control arms by monitoring growth in terms of height and weight over the period of 6 months To measure and compare micronutrient status of intervention and control arms by comparing baseline midline and endline measurements of hemoglobin levels. To measure and compare morbidity rates of intervention and control arms. To measure and compare rates of achievement of child development goals between intervention and control arms using a standardized tool, the Caregiver Reported Early Development Instrument (CREDI). To understand and record experiences relating to the use of KOKOPlus of mothers/caregivers in the intervention arm through focus group discussion

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Nutrition Poor, Child Development
Keywords
HIV-Exposed, Nutrient Status, KOKOPlus

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
649 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
KOKOPlus protein and micronutrient powder , a complementary food supplement containing soya powder, sugar and oil along with the essential amino acid lysine and a micronutrient mix was formulated. Two weeks' supply of KOKOPlus sachets will be given to intervention arm participants every fortnight for 6 months to be mixed into any cereal, soup, stew, or other food given to the children.
Arm Title
Control
Arm Type
No Intervention
Arm Description
This arm will receive no supplement and no placebo for the duration of the study.,
Intervention Type
Dietary Supplement
Intervention Name(s)
KOKOPlus protein and micronutrient powder
Intervention Description
KokoPlus, a complementary food supplement was formulated by using linear programming methodology to improve the protein quality as well as the micronutrient and macronutrient content of commonly consumed traditional complementary (baby) foods in Ghana . It contains soya powder, sugar and oil along with the essential amino acid lysine and a micronutrient mix. It complies with WHO's complementary feeding guidelines, FAO/WHO recommended micronutrient intake (RNI) and the WHO's guidelines for protein and essential amino acid intake for children in the age group of 6 to 24 months. A daily supply of KokoPlus achieves 30% of the total recommended energy, 60% of total protein and 40% of total fat requirements from complementary foods. It also meets 35-55% of minimum intake of essential amino acids and 50-150% RNI based on the total daily requirements.
Primary Outcome Measure Information:
Title
Anthropometry
Description
Length-for-age Z score, Weight-for-age Z score. Weight for length Z score
Time Frame
6 months
Title
Haemoglobin
Description
(g/dl), anaemia
Time Frame
6 months
Title
Child developmental Milestones achieved
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Morbidity
Description
Incidence of fever, malaise, loss of appetite
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Mother-infant dyads; HIV positive mothers and children between 6 and 12 months of age attending antiretroviral (ART) Clinics and child HIV Clinics. Exclusion Criteria: Mothers who decline to participate in the study Children with severe acute malnutrition (mid-upper arm circumference <115 mm or a weight-for-height/length <-3 Z-scores of the WHO growth standards). Children on hospital admission Children with diagnosed or apparent congenital conditions such as encephalitis, cleft palate, hole in heart, which negatively affect the child's ability to eat and/or growth.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gloria K Folson
Phone
+233550006053
Email
gfolson@noguchi.ug.edu.gh
First Name & Middle Initial & Last Name or Official Title & Degree
Grace S Tokor
Phone
+233243009116
Email
gracetokor@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gloria K Folson
Organizational Affiliation
Noguchi Memorial Institute for Medical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
37 Military Hospital
City
Accra
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philip Nyinaku
Phone
+233244780608
Email
Nyinakup@yahoo.com
Facility Name
Greater Accra Regional Hospital
City
Accra
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Salomey Frimpong
Phone
+233244038803
Email
stfrimpong23@yahoo.com
Facility Name
Korle-bu Teaching Hospital
City
Accra
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joycelyn Assiment Dame
Phone
+233244251126
Email
joycelyndame1@gmail.com
Facility Name
Princess Marie Louise Children's Hospital
City
Accra
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margaret Niezer
Phone
+233244290394
Email
niezermargaret@yahoo.com
Facility Name
Ashaiman Polyclinic
City
Ashaiman
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adwoa Amoako
Phone
+2336300899
Email
adkonadu@yahoo.co.uk
Facility Name
Tema General Hospital
City
Tema
State/Province
Greater Accra
Country
Ghana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Richard Anthony
Phone
+233244273212
Email
kaniagha@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Supplementation Trial of KOKO Plus Among HIV Exposed Children in Accra

We'll reach out to this number within 24 hrs