First Bites: Complementary Feeding - A Global Network Cluster Randomized Controlled Trial

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).
Recruitment status was  Recruiting
Sponsor:
Collaborators:
Kinshasa School of Public Health
University of Zambia
INCAP, Chiimaltenango, Guatemala
Aga Khan University
University of Colorado, Denver
University of North Carolina, Chapel Hill
University of Alabama at Birmingham
Drexel University
RTI International
Information provided by:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
ClinicalTrials.gov Identifier:
NCT01084109
First received: March 9, 2010
Last updated: NA
Last verified: March 2009
History: No changes posted
  Purpose

The specific aims of this project is to determine the impact of a daily intake of one half ounce of lyophilized meat between 6-18 months of age (0.5 oz for 6-12 mo; 0.75 oz for 12-18 mo) on linear growth velocity, zinc and iron intakes and status, brain growth and neurocognitive development, and infectious disease morbidity in populations traditionally dependent on non-micronutrient fortified plant foods for complementary feeding.


Condition Intervention Phase
Complementary Feeding
Infant Growth
Other: Lyophilized meat
Other: Cereal
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Complementary Feeding - A Global Network Cluster Randomized Controlled Trial

Further study details as provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):

Primary Outcome Measures:
  • Linear growth velocity [ Time Frame: 6 to 18 months of age ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Infant Zinc and Ferritin levels [ Time Frame: 18 months ] [ Designated as safety issue: No ]
  • Bayleys II [ Time Frame: 18 months ] [ Designated as safety issue: No ]
  • Incidence of diarrhea, lower respiratory infection, and malaria [ Time Frame: 6 to 18 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 1200
Study Start Date: July 2008
Estimated Study Completion Date: July 2010
Estimated Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
Daily intake of one half ounce of lyophilized meat between 6-18 months of age (0.5 oz for 6-12 mo; 0.75 oz for 12-18 mo)
Other: Lyophilized meat
Daily intake of one half ounce of lyophilized meat between 6-18 months of age (0.5 oz for 6-12 mo; 0.75 oz for 12-18 mo)
Active Comparator: 2
Daily intake of an equi-caloric fortified cereal as complementary feed from 6 to 18 months.
Other: Cereal
Daily intake of an equi-caloric fortified cereal as complementary feed from 6 to 18 months.

Detailed Description:

Inadequate and inappropriate complementary feeding are major factors contributing to excess morbidity and mortality in young children. Prominent among nutrient inadequacies are those of iron and zinc. While huge campaigns are being mounted to fortify complementary foods and to distribute supplements, the effectiveness of these programs is generally uncertain and they do not reach millions of rural poor. By comparison, little support is being given to local food-based solutions. These not only require diversity of plant foods but appear to require the inclusion of meat to achieve zinc and iron requirements. Local supplies of meat are achievable but only with a concerted international and local effort. To justify this effort requires a multi-site efficacy study, the results of which, if positive, will leave no doubt that the effort required to provide sustainable local sources of meat for complementary feeds is worthwhile. The principal hypothesis to be tested is that daily intake of beef (1 oz/d for 6-12 mo and 1.5 oz/d for 12-18 mo) added to usual primarily plant-derived complementary feeds plus selected repetitive nutrition education messages results in greater linear growth velocity than does a micronutrient (including Zn and Fe) fortified equi-caloric cereal/legume supplement plus the same educational messages. Participants from four sites in the Global Network which have stunting rates > 20%, i.e. Guatemala, Pakistan and Zambia will be randomized by clusters to receive either ½ oz lyophilized beef (equivalent to 1 oz cooked beef)/d or the equi-caloric micronutrient-fortified plant-based supplement (both increasing by 50% at age 1 year). Both groups will receive three repetitive messages delivered by study coordinators and through the local health system as part of integrated health care. These are: provide a thick puree/gruel; feed complementary foods at least three times per day; and maximize dietary diversity. These interventions will be preceded by messages to promote exclusive breast feeding until 6 months and to start complementary feeding promptly at that time as far as possible. The meat or fortified cereal supplement will be provided daily in a group setting for each cluster; as necessary the food intervention and messages will be delivered at home by the assigned community coordinator or alternate. Outcome measures, obtained by a separate group of local, trained assessment workers, include: longitudinal linear growth between 6-18 months (primary outcome); weight and head circumference; assessment of dietary variety and diversity at 6,9,12, and 18 months; indices of iron, zinc and Vitamin B12 status at 18 months; neurocognitive development at 18 months; and incidence of diarrhea and lower respiratory infections. A positive multi-country, multi-culture outcome of this trial will demonstrate the efficacy of a regular intake of meat commencing at age 6 months to achieve nutritionally complete complementary feeding and will provide a strong rationale for global efforts to enhance local supplies of meat and achieve acceptance of meats as complementary food.

  Eligibility

Ages Eligible for Study:   3 Months to 4 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Inclusion criteria for clusters: Each cluster will be a rural community characterized by inhabitants with low income and served by one community health center. A primary criterion is that national or other available statistics indicate a prevalence of stunting (mean length for age Z-scores in second year < -2) of at least 20% in young children.
  • Inclusion criteria for individual families:

    • Infant aged 3-4 months;
    • Primarily or exclusively breast feeding with intent to continue breast feeding through at least 1 year.

Exclusion Criteria:

  • Exclusion criteria for individual families: Exclusion criteria include any population/family that is receiving or likely to receive free or subsidized complementary foods (or infant formula) through the health system or NGOs; any individual families who are feeding or intend to feed fortified infant formula or micronutrient-fortified commercial complementary foods.
  • Exclusion criteria for infants: Infants meeting the following criteria will be excluded from participation:

    1. known congenital anomaly;
    2. infant of multiple births;
    3. known neurological deficit apparent at the time of enrollment (including seizures).
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01084109

Locations
Congo
Kinshasa School of Public Health Recruiting
Karawa, Congo
Contact: Antoinette Tshefu, MD, PhD, MPH     243 810-156-910     antotshe@yahoo.com    
Principal Investigator: Antoinette Tshefu, MD, PhD, MPH            
Guatemala
Institute for Nutrition of Central America and Panama (INCAP) Recruiting
Chiimaltenango, Guatemala
Contact: Manolo Mazariegos, MD     502-2471-3299     mmazarie@turbonett.com    
Principal Investigator: Manolo Mazariegos, MD            
Pakistan
Agha Khan University Recruiting
Karachi, Pakistan
Contact: Omrana Pasha, MD     92-21-486 4948     omrana.pasha@aku.edu    
Principal Investigator: Omrana Pasha, MD            
Zambia
University of Zambia Recruiting
Lusaka, Zambia
Contact: Elwyn Chomba, MBChB, DCH, MRCP     (260-1) 25-46-55     echomba@zamnet.zm    
Principal Investigator: Elwyn Chomba, MBChB, DCH, MRCP            
Sponsors and Collaborators
Kinshasa School of Public Health
University of Zambia
INCAP, Chiimaltenango, Guatemala
Aga Khan University
University of Colorado, Denver
University of North Carolina, Chapel Hill
University of Alabama at Birmingham
Drexel University
RTI International
  More Information

No publications provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Linda Wright, Eunice Kennedy Shriver National Institute of Child Health and Human Development
ClinicalTrials.gov Identifier: NCT01084109     History of Changes
Other Study ID Numbers: GN CF
Study First Received: March 9, 2010
Last Updated: March 9, 2010
Health Authority: United States: Federal Government

Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
Complementary feeding
Infant growth
Developing countries

ClinicalTrials.gov processed this record on May 21, 2013