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BRAIN - Home Intervention Trial (BRAIN-HIT)

Primary Purpose

Asphyxia

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Early intervention counseling
Health education counseling
Sponsored by
NICHD Global Network for Women's and Children's Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asphyxia focused on measuring asphyxia, neurodevelopmental outcome, home counseling

Eligibility Criteria

1 Minute - 28 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • birth asphyxia
  • birth weight of at least 1,500g
  • neurological examination consistent with normal, Stage I or II on the Ellis scale (Ellis, et al. 2000)
  • willing to participate in an intervention program for 36 months.

Exclusion Criteria:

-

Sites / Locations

  • JN Medical College
  • Aga Khan University
  • University of Zambia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Home intervention program

health education counseling

Outcomes

Primary Outcome Measures

neurodevelopmental outcome

Secondary Outcome Measures

The improvements in cognitive, social, and motor development will be larger in the infants who have had birth asphyxia compared to those without birth asphyxia.
The effects of EI in infants with and without birth asphyxia will be moderated by child and family characteristics.

Full Information

First Posted
March 18, 2008
Last Updated
July 29, 2014
Sponsor
NICHD Global Network for Women's and Children's Health
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1. Study Identification

Unique Protocol Identification Number
NCT00639184
Brief Title
BRAIN - Home Intervention Trial
Acronym
BRAIN-HIT
Official Title
Brain Research to Ameliorate Impaired Neurodevelopment (BRAIN): Home-based Intervention A Multicenter Trial of the Global Network for Women's and Children's Health Research
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NICHD Global Network for Women's and Children's Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We plan to test a home-based parent-provided early developmental intervention (EI) both in infants with mild to moderate birth asphyxia and in infants without perinatal complications who will constitute a healthy comparison group in a randomized controlled trial. The trial will evaluate the effect of a resource-intensive early intervention (EI) program on the outcomes in infants born in rural communities in Zambia, India, and Pakistan. It will consist of frequent interaction (every 2 weeks the first year and every 4 weeks the second and third years) between parents and the parent trainer. The control group will receive enhanced health counseling (HC). The overall goal will be to implement and evaluate an EI program for infants following birth asphyxia, which is sustainable in developing countries. The challenge will be to adapt programs demonstrated to be effective in developed countries to the circumstances of the developing world, while reducing the demands on resources. Because there are limited data on normative development and EI programs in developing countries, a group of infants without perinatal complications will also be randomized to the same conditions in order to provide a comparison of what may be achieved from the intervention in healthy infants in developing countries. A final aim will be to address individual variation in EI effects that could be due to child and/or family characteristics. A randomized controlled experimental design will be used, in which infants who survive following birth asphyxia are randomly assigned to either EI or enhanced health education counseling (HC). The trial will randomize infants to a home-based parent-provided early developmental intervention (EI) with frequent home interaction between parents and parent trainers vs. HC. A group of infants without birth asphyxia or other major perinatal complications also will be randomized. Children will be examined by masked examiners at three time points (12, 24, and 36 month's assessments).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asphyxia
Keywords
asphyxia, neurodevelopmental outcome, home counseling

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Home intervention program
Arm Title
2
Arm Type
Active Comparator
Arm Description
health education counseling
Intervention Type
Other
Intervention Name(s)
Early intervention counseling
Intervention Description
Bi-monthly home visits by counselor
Intervention Type
Other
Intervention Name(s)
Health education counseling
Intervention Description
World Health Education health education counseling program at home visits,twice per month
Primary Outcome Measure Information:
Title
neurodevelopmental outcome
Time Frame
36 months
Secondary Outcome Measure Information:
Title
The improvements in cognitive, social, and motor development will be larger in the infants who have had birth asphyxia compared to those without birth asphyxia.
Time Frame
12, 24 and 36 months
Title
The effects of EI in infants with and without birth asphyxia will be moderated by child and family characteristics.
Time Frame
12, 24 and 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
28 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: birth asphyxia birth weight of at least 1,500g neurological examination consistent with normal, Stage I or II on the Ellis scale (Ellis, et al. 2000) willing to participate in an intervention program for 36 months. Exclusion Criteria: -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marion Koso-Thomas, MD
Organizational Affiliation
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Wally A Carlo
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
JN Medical College
City
Belgaum
Country
India
Facility Name
Aga Khan University
City
Karachi
Country
Pakistan
Facility Name
University of Zambia
City
Lusaka
Country
Zambia

12. IPD Sharing Statement

Citations:
PubMed Identifier
22099522
Citation
Carlo WA, Goudar SS, Pasha O, Chomba E, McClure EM, Biasini FJ, Wallander JL, Thorsten V, Chakraborty H, Wright LL; Brain Research to Ameliorate Impaired Neurodevelopment-Home-based Intervention Trial Committee; National Institute of Child Health and Human Development Global Network for Women's and Children's Health Research. Neurodevelopmental outcomes in infants requiring resuscitation in developing countries. J Pediatr. 2012 May;160(5):781-5.e1. doi: 10.1016/j.jpeds.2011.10.007. Epub 2011 Nov 17.
Results Reference
derived
PubMed Identifier
20433740
Citation
Wallander JL, McClure E, Biasini F, Goudar SS, Pasha O, Chomba E, Shearer D, Wright L, Thorsten V, Chakraborty H, Dhaded SM, Mahantshetti NS, Bellad RM, Abbasi Z, Carlo W; BRAIN-HIT Investigators. Brain research to ameliorate impaired neurodevelopment--home-based intervention trial (BRAIN-HIT). BMC Pediatr. 2010 Apr 30;10:27. doi: 10.1186/1471-2431-10-27.
Results Reference
derived

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BRAIN - Home Intervention Trial

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