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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01841151
Other study ID # KITE
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2013
Est. completion date October 2020

Study information

Verified date August 2021
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if neurofeedback and working memory training improves core symptoms of ADHD in children and adolescents.


Description:

This study investigates two types of Neurofeedback (NF), one well-established and well-researched protocol called Slow Cortical Potential NF (SCP), and a newer and less researched, yet popular among private clinicians, the so-called live z-score training (LZT). These methods are compared to working memory training (WMT) and a passive control condition, treatment-as-usual only (TAU). The active conditions (SCP/LZT/WMT) are delivered high frequent, with 5 sessions/week, for a total of 25 sessions. Outcomes measures are taken at Preintervention and Postintervention, as well as at a 6-month follow-up assessment.


Recruitment information / eligibility

Status Completed
Enrollment 202
Est. completion date October 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 9 Years to 17 Years
Eligibility Inclusion Criteria: - Clinical AD/HD diagnose according to DSM-IV-TR and K-SADS interview, 9-17 years old, unmedicated or under stable medication with stimulants or corresponding since at least one month. Exclusion Criteria: - IQ <70 (WISC-IV or WAIS-IV), clinically instable psychiatric state e.g. severe depression, OCD, self-injurious behaviour, bipolar disorder, severe somatic (neurologic) disease, very limited knowledge in the Swedish language.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SCP training

Live Z-score training

WM training


Locations

Country Name City State
Sweden Cap Bup-Kind Stockholm

Sponsors (5)

Lead Sponsor Collaborator
Karolinska Institutet Child and Adolescent Psychiatry, Stockholm, Region Stockholm, Stiftelsen Sunnerdahls Handikappfond, Swedish Foundation for Strategic Research

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Conners 3 Self-, parents- and teachers report. Outcome measures will be conducted before and after five weeks training, and at 6 months follow-up. Up to seven months
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