Follow-up Evaluation of Home Nurse Visitation Program for Socially Disadvantaged Women and Their Children

NCT00443586 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 345

Last updated 2021-06-10

No results posted yet for this study

Summary

This study will evaluate the long-term effects of a prenatal and early childhood home nurse visitation program for socially disadvantaged women and their children.

Conditions

  • Risk Reduction Behavior

Interventions

BEHAVIORAL

Developmental Screening

Child participants were screened for sensory and developmental problems and referred for further evaluation and treatment at ages 12 and 24 months of age

BEHAVIORAL

Screening plus Transportation

Child participants were screened for sensory and developmental problems and referred for further evaluation and treatment at 12 and 24 months of age; their mothers were provided with free transportation for prenatal and well-child care through child age 2.

BEHAVIORAL

Screening, Transport, Prenatal Visits

Child participants were screened for sensory and developmental problems and referred for further evaluation and treatment at 12 and 24 months of age; their mothers were provided with free transportation for prenatal and well-child care through child age 2, and were provided an average of 9 home visits by nurses during pregnancy.

BEHAVIORAL

Screen, Transport, Prenatal/Inf Visits

Child participants were screened for sensory and developmental problems and referred for further evaluation and treatment at 12 and 24 months of age; their mothers were provided with free transportation for prenatal and well-child care through child age 2, and were provided an average of 9 home visits by nurses during pregnancy and 23 during the child's first two years of life.

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • University of Colorado, Denver

    lead OTHER

Principal Investigators

  • David L. Olds, PhD · University of Colorado, Denver

  • John Eckenrode, PhD · Cornell University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
27 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2004-09-30
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00443586 on ClinicalTrials.gov