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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03175185
Other study ID # 17100221
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 1, 2017
Last updated June 1, 2017
Start date November 2017
Est. completion date November 2019

Study information

Verified date June 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to carry out a psychological evaluation for the parents of children diagnosed with attention deficit hyperactivity disorder (ADHD) and parents of children without ADHD as control to detect any psychological problems in those of children with ADHD . These problems may be a precipitating factor to cause ADHD in their child or have a genetic predisposition to be passed to their children. On the other hand these psychological problems may be caused by the difficulties they encounter in raising their ADHD child. The exact relation needs more researches and to be more investigated.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date November 2019
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Parents of children diagnosed with ADHD according to the American Psychiatric Association's Diagnostic and Statistical Manual (DSM-V).

- Children are between 4 and 16 years of age for both sexes.

- Children with normal IQ > 70%.

- Parents are able to give informed consent and able to complete the research assessments.

Exclusion Criteria:

- Parents having chronic debilitating diseases e.g. chronic liver cirrhosis.

- Parents were participating in other clinical research.

- Refusal to participate.

Study Design


Related Conditions & MeSH terms

  • Attention Deficit Disorder with Hyperactivity
  • Attention Deficit Hyperactivity Disorder
  • Hyperkinesis

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Psychiatric Assessment of the parents Detection of personality disorders, anxiety and depressive symptoms 2 years
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