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临床试验/NCT03329625
NCT03329625已完成不适用

PREVENTING CONDUCT DISORDER AMONG CHILDREN IN THE CHILD WELFARE SYSTEM

Washington University School of Medicine0 个研究点目标入组 144 人开始时间: 2010年7月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
144
主要终点
Eyberg Child Behavior Inventory

研究概览

简要总结

A mixed methods randomized control trial was conducted to test the effectiveness of Pathways Triple P with child welfare involved families compared to treatment as usual. Outcomes tested included parenting behaviors and attitudes, and child behavior problems. 144 families were recruited into the study. Data was collected at 4 time points (baseline, 4 months, 9 months, and 18 months). Over 70% were retained from baseline to 18 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Families with open child protective service case following allegation of child physical abuse or neglect
  • parent of child between the age of 3 and 12
  • Child remained in the home following investigation
  • parent spoke English

排除标准

  • parent's child could not have chronic medical condition or have a pervasive developmental delay

研究组 & 干预措施

Pathways Triple P

Experimental

Families randomized to the Pathways Triple P received a 14 week home based intervention.

干预措施: Pathways Triple P (Behavioral)

Services as Usual

Active Comparator

Families randomized to the services as usual condition received services as usual through the Missouri Children's Division

干预措施: Services as Usual (Behavioral)

结局指标

主要结局

Eyberg Child Behavior Inventory

时间窗: 18 months

Child Behavior Problems

PedsQL

时间窗: 18 months

Pediatric Quality of Life Scale

次要结局

  • Parenting Stress Inventory(18 months)
  • Parent Anger Inventory(18 months)
  • Parental Sense of Competence(18 months)
  • Alabama Parenting Questionnaire(18 months)
  • Depression Anxiety Stress Scales(18 months)
  • AUDIT(18 months)
  • The Drug Abuse Screening Test(18 months)
  • HITS IPV Screening(18 months)
  • PQL(18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Patricia Kohl, Ph.D.

Associate Professor

Washington University School of Medicine

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