"Investigation of the Effectiveness of a Motor Therapy Program (Self-Training) Using a Sensory Integration Perspective"

"Investigation of the Effectiveness of a Motor Therapy Program (Self-Training) Using a Sensory Integration Perspective-An Attempt to Address Clumsiness in Children with Autism Spectrum Disorder"

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT1040250132

Enrollment

110

Registered

2025-12-01

Start date

2023-07-10

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Autism Spectrum Disorder ASD

Interventions

In addition to the three sensory integration therapy sessions during and after the inpatient program, participants will be asked to perform individual motor tasks at home as self-training (3-4 exercis

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: This study targets 5-6 year old children with ASD and their guardians who participated in a one-week inpatient program (Pikaichi Program) between October 2022 and March 2028, and who meet the following inclusion criteria and none of the exclusion criteria: Completed three sessions of sensory integration therapy during and after the inpatient program. Scored below -1 standard deviation from the age-appropriate mean on any 8 items of the M-ABC2 assessment (indicating clumsiness).

Exclusion criteria

Exclusion criteria: 1.The child's developmental intelligence test around 6 years of age shows an IQ below 70. 2. The child has motor paralysis due to a neurological or muscular disease that affects daily life. 3. The child and/or guardian do not consent to participate in the study (or withdraw consent during the study). 4. Major outcome data (M-ABC2, DCDQ-R, SP Sensory Profile, ADHD-RS, SDQ) could not be obtained for any reason. 5.The period for performing motor tasks (motor therapy program) after the inpatient program is less than a total of 4 weeks.

Design outcomes

Primary

Measure	Time frame
For the target children: M-ABC2 For the guardians: Sensory Profile, DCDQ-R Japanese version, PARS-TR, ADHD-RS, SDQ	—

Contacts

Public ContactRyo Hashitani

Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital

hashitani.nagoyadai2@gmail.com+81-52-832-1121

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026