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MOM Program 8-Year Follow-up

NCT00970853 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 187

Last updated 2014-04-15

Study results available
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Summary

Study measures will evaluate cognitive, academic, and behavioral outcomes for the children, school services received, and caregiver stress and depression. The main study outcome measures include cognitive status, school functioning, and behavior. Long-term outcomes will be studied in attempt to verify the 33 and 60 month significant differences found in school participation and behavior between the intervention and control groups.

Conditions

  • Child Development

Interventions

BEHAVIORAL

MOM Program home visiting

Mixed professional home visiting program.

OTHER

Control

Control group will receive same assessment batteries at follow-up but did not receive the home visiting program.

Sponsors & Collaborators

Principal Investigators

  • Jerilynn Radcliffe, PhD · Children's Hospital of Philadelphia

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
94 Months
Max Age
98 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-03-31
Primary Completion
2011-05-31
Completion
2011-05-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00970853 on ClinicalTrials.gov