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Clinical Trials/NCT04201509
NCT04201509
Completed
Not Applicable

Validity of Neurocognitive Assessment Methods in Childhood ADHD

Region Skane1 site in 1 country196 target enrollmentJune 1, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neurodevelopmental Disorders
Sponsor
Region Skane
Enrollment
196
Locations
1
Primary Endpoint
Emotional status assessed with the Beck Youth Inventory.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of the study is to examine the prospective validity of neurocognitive functions and emotional factors in schoolchildren with ADHD and a control group of typically developing schoolchildren at baseline and after three years.

Detailed Description

In spite of extensive research on children with ADHD, there is still insufficient understanding of the discriminative validity of neurocognitive tests and how test results of neurocognitive functions and ratings of emotional factors and ADHD symptoms change over time and interacts during development. The project is studying the validity of clinical assessment methods within the Swedish child and adolescent psychiatry service (CAP) related to the identification of ADHD, additional impairments, and comorbidity. The prospective validity of neurocognitive functions and emotional factors in schoolchildren with ADHD and a control group of typically developing schoolchildren at baseline and after three years will be investigated. Specific aims: Aim I: Study how attentiveness and impulsivity in ADHD change over three years by comparing the results of psychological tests and rating scales at baseline and after three years Aim II: Study intellectual development in ADHD by comparing the results of intelligence tests at baseline and after three years- Aim III: Study how emotional factors change over three years by comparing the results of rating scales at baseline and after three years

Registry
clinicaltrials.gov
Start Date
June 1, 2011
End Date
November 1, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The ADHD-group:
  • The individuals were assessed and diagnosed with ADHD at the Neuropsychiatric Unit of the CAP Clinic in Lund in 2011-2012
  • Non-clinical group:
  • School children from Lund.

Exclusion Criteria

  • If the individual had a diagnosed intellectual disability
  • If the individual required an interpreter to participate in the study

Outcomes

Primary Outcomes

Emotional status assessed with the Beck Youth Inventory.

Time Frame: 2011-2012 and 2014-2015

The children were assessed with the Beck youth scales at two timepoints with a time interval of 3 years. Beck Youth Inventory consist of 5 subscales, Depression, Anxiety, Anger, Disruptive behaviour, Self-concept. It is standardized into percentiles and higher scores mean worse behaviour, except for Self-concept. In Self-concept higher scores mean better behaviour.

Secondary Outcomes

  • Neuropsychological status assesses with the Conners' Continuous Performance Test (CPT) II(2011-2012 and 2014-2015)

Study Sites (1)

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