Early Home Visitation Program to Promote Good Health and Development in Children at Risk for Abuse

September 23, 2013 updated by: Johns Hopkins University

Promoting Child Mental Health: RCT of Home Visiting

This study will evaluate the effectiveness of Hawaii's Healthy Start Program (HSP), a home visitation program for families at risk for child abuse, in promoting the health and development of children.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Hawaii's Healthy Start Program (HSP) is a well-respected home visiting program for families at risk for abuse of their newborn children. The program incorporates early identification of at-risk families. Each family then begins receiving long-term home visitations. The home visiting component aims to promote child health and development and to prevent child abuse by improving family functioning and parenting. Home visitors are trained paraprofessionals working under professional supervision. The program includes both direct services and referrals to community resources. Direct services include providing emotional support to parents, encouraging them to seek needed professional help, teaching parents about child development, and role-modeling parenting skills and problem-solving techniques. In a previous study, at-risk families were randomly assigned to either HSP or no intervention. Evaluations were conducted at the time of the child's birth and at ages 1, 2, and 3 in order to assess the home environment and the development and well-being of the child. This study is a continuation study. Participants will include the original families from the previous study, as well as a new group of families who are not at risk for child abuse. By interviewing and observing these two groups of families, this study will evaluate the effectiveness of HSP in promoting children's mental health, cognitive and social-emotional development, and academic achievement in the first years of school.

All families will be evaluated on a yearly basis when the child is in 1st, 2nd, and 3rd grade. Interviews will be conducted with the parents, children, and teachers. Parent interviews will focus on family functioning, including mental health of the parents, parenting attitudes and behaviors, quality of the home environment, and any domestic violence or substance abuse that occurred. In addition, the child's health and development, as well as use of any community resources will be assessed. Interviews with the children and teachers will focus on assessing the child's behavior and emotional well-being. The family's home environment, the interaction between the parents and children, and the children's classroom behavior will be observed. Each child will also undergo developmental testing. All measurements will be collected at each yearly visit.

Study Type

Interventional

Enrollment

1122

Phase

  • Phase 2
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hawaii
      • Honolulu, Hawaii, United States, 96814
        • Johns Hopkins University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Families in the Oahu community who delivered newborns between November 1994 and November 1995
  • If enrolled in the control group, must not have been previously enrolled in Hawaii's Healthy Start Program

Exclusion Criteria:

  • Insufficient understanding of English

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Child cognitive development, behavior, and health
Time Frame: At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
Child social-emotional development
Time Frame: At-risk sample: Up to 6 years; Not-at risk sample: Up to 1 year
At-risk sample: Up to 6 years; Not-at risk sample: Up to 1 year
Child depression
Time Frame: At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years

Secondary Outcome Measures

Outcome Measure
Time Frame
Family functioning
Time Frame: At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
Parent functioning and stress levels
Time Frame: At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
Substantiated reports of child abuse
Time Frame: At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years
At-risk sample: Up to 8 years; Not-at risk sample: Up to 2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Anne K. Duggan, ScD, Johns Hopkins University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2000

Primary Completion (Actual)

June 1, 2005

Study Completion (Actual)

August 1, 2005

Study Registration Dates

First Submitted

September 16, 2005

First Submitted That Met QC Criteria

September 16, 2005

First Posted (Estimate)

September 22, 2005

Study Record Updates

Last Update Posted (Estimate)

September 24, 2013

Last Update Submitted That Met QC Criteria

September 23, 2013

Last Verified

February 1, 2008

More Information

Terms related to this study

Other Study ID Numbers

  • R01MH060733 (U.S. NIH Grant/Contract)
  • DSIR CT-P (Other Identifier: NIMH)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Child Abuse

Clinical Trials on Home Visiting

3
Subscribe