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Effects of Fairytales on Preschool Children With Attention Deficit Hyperactivity Disorder

T

Taipei Medical University

Status

Not yet enrolling

Conditions

Preschool Children
Attention Deficit Hyperactivity Disorder
Developmental Delay

Treatments

Other: Traditional rehabilitation programs with Individualized fairytales class

Study type

Interventional

Funder types

Other

Identifiers

NCT05502536
2022SKHADR033

Details and patient eligibility

About

Under traditional rehabilitation programs, investigate the additional effects of individualized fairytales on preschool children with Attention Deficit Hyperactivity Disorder with developmental delays.

Full description

Thirty preschool children with Attention Deficit Hyperactivity Disorder and developmental delays will be enrolled in regular traditional rehabilitation programs.

They will be randomized to the intervention group and control group. The participants in the intervention group will receive an additional 30 minutes per week for 12 sessions of individualized fairytales classes by a child and educational teacher for three months. The participants of both groups will continue to receive the traditional rehabilitation programs.

Therapeutic effects, including attention, cognitive function, vocabulary function, physical functional performance, and quality of life at baseline, will be evaluated after 12 weeks of treatment and three months after the treatment.

The evaluator will be blinded to the group's allocation during the whole course of the intervention.

Enrollment

30 estimated patients

Sex

All

Ages

3 to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • preschool children with a diagnosis of Attention Deficit Hyperactivity Disorder and developmental delay, under regular traditional rehabilitation programs, intelligence quotient 70 or greater

Exclusion criteria

  • age less than 3 or greater than 6 of children diagnosed with Attention Deficit Hyperactivity Disorder and developmental delay, under regular traditional rehabilitation programs, intelligence quotient below 70

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Intervention group
Experimental group
Description:
traditional rehabilitation programs with additional individualized fairytales class
Treatment:
Other: Traditional rehabilitation programs with Individualized fairytales class
Control group
No Intervention group
Description:
traditional rehabilitation programs without additional individualized fairytales class

Trial contacts and locations

1

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Central trial contact

Ru-Lan Hsieh, MD

Data sourced from clinicaltrials.gov

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