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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03632629
Other study ID # 2018SKHADR028
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 2018
Est. completion date March 2019

Study information

Verified date August 2018
Source Taipei Medical University
Contact Ru-Lan Hsieh, MD
Phone +886228332211
Email M001052@ms.skh.org.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Using a single blind, randomized controlled design to study the additional therapeutic effects of cognitive training on traditional rehabilitation programs for children with attention deficit hyperactivity disorder and developmental delays.


Description:

A total of 30 children with attention deficit hyperactivity disorder and developmental delays who are receiving traditional rehabilitation programs will be enrolled.

The participants will be randomized into two groups, including study group (traditional rehabilitation program with additional cognitive training: 2 times per week, 15 min per session, a total of 24 sessions) and control group (traditional rehabilitation program without additional cognitive training).

Memory related functions, quality of life, and physical function evaluations will be performed at baseline, 3 months and 6 months later, respectively.

Evaluator will be blinded to the group's classification during the whole course of study.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date March 2019
Est. primary completion date March 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 8 Years
Eligibility Inclusion Criteria:

- children diagnosed with attention deficit hyperactivity disorder with developmental delay receiving regular rehabilitation programs intelligence quotient 70 or greater

Exclusion Criteria:

- age less than 4 years or elder than 8 years children diagnosed with attention deficit hyperactivity disorder receiving regular rehabilitation programs intelligence quotient less than 70

Study Design


Related Conditions & MeSH terms

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

Intervention

Other:
interactive cognitive training
Using interactive brain club system training to children with attention deficit hyperactivity disorder with developmental delay

Locations

Country Name City State
Taiwan Shin Kong Wu Ho-Su Memorial Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of attention score assessed by Swanson, Nolan and Pelham questionnaire scores change from baseline to 3 months of treatment, and 3 months after treatment
Secondary change of visual motor integration score assessed by Beery-Buktenica Visual Motor Integration Test scores change from baseline to 3 months of treatment, and 3 months after treatment
Secondary change of sensory integration score assessed by Sensory Profile questionnaire scores change from baseline to 3 months of treatment, and 3 months after treatment
Secondary change of intelligence score assessed by Wechsler Intelligence Scale for Children, including verbal, performance and total scores, the average score is 100, with higher scores indicating higher than average intelligence and lower scores indicating lower levels of intelligence scores change from baseline to 3 months of treatment, and 3 months after treatment
Secondary change of functional performance score assessed by Pediatric Outcome Data Collection Instrument changes from baseline to 3 months of treatment, and 3 months after treatment
Secondary change of health-related quality of life score assessed by Pediatric Quality of Life Inventory-Generic Core Scales, including physical, psychosocial, and total scores, with higher scores representing better health-related quality of life changes from baseline to 3 months of treatment, and 3 months after treatment
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