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Clinical Trials/ISRCTN26270684
ISRCTN26270684
Completed
N/A

Psychoeducation in families of children with attention deficit hyperactivity disorder (ADHD) in the United Kingdom: evaluation of the efficacy in a randomised controlled trial and a qualitative examination of the program

Kings College London (UK)0 sites70 target enrollmentFebruary 24, 2010
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ConditionsAttention deficit disorder (ADD)/attention deficit hyperactivity disorder (ADHD)Mental and Behavioural DisordersHyperkinetic disorders

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention deficit disorder (ADD)/attention deficit hyperactivity disorder (ADHD)
Sponsor
Kings College London (UK)
Enrollment
70
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 24, 2010
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Kings College London (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. Diagnosis of attention deficit disorder (ADD)/attention deficit hyperactivity disorder (ADHD) in child (Diagnostic and Statistical Manual of Mental Disorders, 4th Edition \[DSM\-IV]), with most of their co\-morbidity represented (except for the exclusion criteria), and any treatment prescribed
  • •2\. Age of child between 4 and 19 years, either sex
  • •3\. Informed consent of the parents and the children available
  • •4\. Parents' age greater than or equal to 18 years
  • •5\. Responsibility and legal capacity in parents
  • •6\. Participant on clinical ADHD symptoms stabilisation for at least 1 month before entering the study (with or without medical treatment)

Exclusion Criteria

  • •1\. Severe Autistic Spectrum Disorders (\*)
  • •2\. Severe learning disabilities (\*)
  • •3\. Earlier or current participation in other intervention trials that might interfere with the current study
  • •(\*) due to added problems to ADHD, thus requiring a different sort of intervention

Outcomes

Primary Outcomes

Not specified

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