跳至主要内容
临床试验/EUCTR2010-019930-28-NL
EUCTR2010-019930-28-NL进行中(未招募)不适用

The effectiveness of Parent-Child Interaction Therapy versus methylphenidate in preschool children with ADHD and disruptive behavior problems with insufficient improvement through Parent Management Training. - STAP

Accare0 个研究点目标入组 60 人开始时间: 2010年3月31日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Children of both sexes, of any ethnic and cultural background, ages 2;6 to 5;6 years.
  • 2.At time of referral A DSM-IV (American Psychiatric Association, 1994) consensus diagnosis of ADHD any subtype including ADHD-Not Otherwise Specified.
  • 3.At time of referral presence of oppositional behavior as evidenced through either a DSM-IV (American Psychiatric Association, 1994) consensus diagnosis of ODD, or Conduct Disorder, or Disruptive Behavior Disorder Not Otherwise Specified, or a baseline mother’s ECBI score > 114 and identification of minimally three target problem behaviors.
  • 4.Previous treatment through PMT has resulted in less than 30% reduction on the ECBI, or on the Externalizing scale of the Teacher Report Form for Ages 1½-5 (TRF/1½-5) or has resulted in a rating of less than improved on the Clinical Global Impression Scale of improvement by at least two of the three raters (parent, teacher, or clinician).
  • 5.Full Scale IQ equivalent of >70.
  • 6.The same primary caretaker for at least 6 months before inclusion.
  • 7.Parents have provided informed consent to participate in the study, in accordance with Dutch ethical regulations.
  • 8.Systolic and diastolic blood pressure below 95th percentile for age and gender.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Previous PCIT; other forms of previous treatments are acceptable, including the use of previous psychotropic medication.
  • 2.The child has a major medical condition that would interfere with involvement in a long-term study or could be affected negatively by methylphenidate.
  • 3.Ongoing psychosocial treatment or ongoing treatment with psychotropic medication.
  • 4.Inability of the parent to understand or follow study instructions.
  • 5.Patients whose families anticipate a move outside the geographic range of the investigative site or who plan extended travel inconsistent with the recommended visit intervals.
  • 6.Use of any other psychotropic medication or has taken an investigational drug in the past 30 days.

研究者

发起方
Accare

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