University of Oklahoma Parenting Program Attrition

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

450 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-01-31

Study Completion Date

2006-09-30

Brief Summary

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The study will examine the extent to which a group motivational intervention (ME) impacts retention, treatment compliance, and long-term outcomes in families with a history of, or high risk for, child maltreatment.

Detailed Description

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The field of child abuse prevention faces not only the challenge of developing and disseminating effective treatments, but the problem of high attrition rates and treatment noncompliance. This study will compare the effects of a motivational intervention with a "services as usual" orientation group on program retention, treatment compliance, and long-term outcomes in families with histories of child maltreatment.

Conditions

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Child Abuse

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Interventions

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Motivational intervention, parent training

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Families referred to service agency for child maltreatment prevention services
* Families with children between 2-1/2 and 12 years of age

Exclusion Criteria

* Parents with cognitive, psychiatric, or social conditions that would limit their ability to provide voluntary consent or benefit from the intervention
* Parents who have sexually abused their children

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Principal Investigators

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Mark J Chaffin, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of Oklahoma

Locations

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University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, United States

Site Status

Countries

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United States

Other Identifiers

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R49/CCR622338-04

Identifier Type: -

Identifier Source: secondary_id

CDC-NCIPC-3899