A Study on the Evaluation of Effectiveness, such as Cognitive Improvement of Programs for Children's Cognitive Improvement

Single-institution, single-blindness, and exploratory clinical trials for evaluating effectiveness, including cognitive improvement in computerized cognitive rehabilitation programs (D-kit/EF1), for children with normal developmental intelligence (FSIQ85) or lower

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007847

Enrollment

Registered

2022-10-25

Start date

2022-10-22

Completion date

Unknown

Last updated

2022-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : D-kit/EF1 is a mobile application developed to improve children's cognition for children of 48-84 months of cognitive age, and is produced in a game-type manner that provides quizzes suitable

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: A. Selection criteria If you satisfy all four of the following: 1. Based on KCD-7, the Korean standard disease classification code, children between the ages of 4-7 who were diagnosed by doctors with mental retardation (F70-F79), or disorder of psychological development (F80-F89) 2. Children with normal developmental intelligence (FSIQ 84) or lower 3. Children who are not planned to change the number and content of rehabilitation treatment and drug treatment such as personal teaching and physical therapy, occupational therapy, cognitive therapy, and speech therapy during the study period 4. Patients whose legal guardian has agreed to this study

Exclusion criteria

Exclusion criteria: C. Except where any of the following criteria are included 1. Patients with a clear history of acquired brain damage such as cerebral palsy 2. Children with vision or hearing problems who cannot perform D-kit/EF1 3. Patients who show delays in development of large muscles or small muscles to the point where D-kit/EF1 cannot be performed 4. Patients who are judged to have emotional and social problems to the extent that D-kit/EF1 cannot be implemented 5. Children whose legal guardian did not agree with this study 6. In the case where the patient does not express his/her consent 7. Where it is deemed difficult for the research manager to participate due to other reasons;

Design outcomes

Primary

Measure	Time frame
Dimensional Change Card Sort (DCCS) section of the NIH Toolbox	—

Secondary

Measure	Time frame
PsychoEducational Profile Revised, PEP-R;K-Vineland-II;Childrens Color Trails Test, CCTT;Advanced Test of Attention, ATA;Verbal Fluency Test	—

Countries

Korea, Republic of

Contacts

Public ContactSoon-Beom Hong

Seoul National University Hospital

hsbmdmore@hanmail.net+82-2-0000-0000

Outcome results