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Not yet recruitingNCT07656961Updated Jun 18, 2026

Ayres Sensory Integration Test Evaluation Results and Neurodevelopmentally Focused Counseling in Children With Neurodevelopmental Problems

An observational study in Sensory Processing Disorder and Neurodevelomental Disorders, sponsored by Yeditepe University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 3 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-18.

Sponsored by Yeditepe University · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
16
Ages
3 Years to 12 Years
Sex
All
01

Study summary

The aim of the study is to investigate the long-term effects of ASI-based and hybrid neurodevelopmental counseling services on the variables of the Ayres Sensory Integration Assessment Test in children with neurodevelopmental disorders.

Read the detailed description

After application to the YUGEM Sensory Perception Motor Unit, the child and family will undergo a preliminary assessment. Following the necessary interviews and psychiatric consultation, specialists will decide whether the child is suitable for the Evaluation in Ayres Sensory Integration (EASI).

Children who are considered suitable for the EASI assessment will be evaluated through a multidisciplinary approach. The data obtained from the assessment will be analyzed using computer-based statistical software, and the results will be reviewed by the specialists. Based on these results, the frequency, duration, and delivery method of sensory integration therapy will be determined according to the needs of the child and family.

Neurodevelopmentally focused therapy counseling based on Ayres Sensory Integration principles will be planned either face-to-face or remotely, as appropriate for the child and family. After this decision, a meeting will be held with the family to plan the child's therapy process. There will be a 6-month therapy-counseling process.

02

Conditions studied

  • Sensory Processing Disorder
  • Neurodevelomental Disorders

Keywords

  • Neurodevelopmental Disorders
  • Sensory Integration
  • EASI
03

In context

Neurodevelopmental Disorders

352 studies on the registry are indexed under Neurodevelopmental Disorders; 141 are open to participants now.

This study's planned enrollment of 16 is below the median of 200 across 133 observational studies indexed under Neurodevelopmental Disorders.

Browse Neurodevelopmental Disorders studies →

Lead sponsor

Yeditepe University is the lead sponsor of 131 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of children aged 3 to 12 years with diagnosed or suspected neurodevelopmental problems who apply to the YUGEM Sensory Perception Motor Unit at Yeditepe University. Children referred for neurodevelopmental follow-up and considered suitable for the Evaluation in Ayres Sensory Integration assessment will be included in the study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 3-12
  • Sensory sensitivity (excessive or under-reaction to tactile, movement, auditory, or visual stimuli)
  • Have been referred by a pediatrician for neurodevelopmental monitoring
  • Have coordination difficulties
  • Difficulty organizing gross and/or fine motor movements
  • Activity level significantly above or below the norm for their age
  • Delays in academic achievement
  • Difficulties with daily living skills such as dressing and personal hygiene

Exclusion criteria

Exclusion Criteria:

  • Being under 3 years of age or over 12 years of age
  • Having no conditions that fall outside normal developmental parameters
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
16 participants (estimated)
Target follow-up
1 Month
Patient registry
Yes

Groups and cohorts

  • Children With Neurodevelopmental Disorders

    Children aged 3 to 12 years with neurodevelopmental disorders who applied to the YUGEM Sensory Perception Motor Unit and are considered suitable for the Evaluation in Ayres Sensory Integration assessment.

06

What researchers measure

Primary outcomes

  1. The Evaluation of Ayres Sensory Integration (EASI)

    The Evaluation of Ayres Sensory Intergation test measures sensory perception, postural/ocular/bilateral motor integration, praxis, and sensory reactivity in a way that minimizes the effects of culture, language comprehension, and prior experience. The EASI tests are designed for children aged 3-12 and will be administered by appropriately trained professionals.

    Time frame: 4 Weeks

  2. Pediatric Sensory Profile

    This is a measure consisting of three main sections used in children. These are; sensory processing, modulation and behavioral and emotional responses. The subgroups of each main section (14 sections in total, 125 questions) are tested. This scale is administered by the caregiver.

    Time frame: 4 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided — It's not decided.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2026; primary completion for Jul 2026, 0 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 15, 2026
First posted
Jun 18, 2026
StartEst.
Jun 18, 2026
Primary completionEst.
Jul 16, 2026
CompletionEst.
Jan 16, 2027
Last update
Jun 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07656961
Responsible party
Elif Develi (Assistant Professor, Yeditepe University) — Principal investigator
First posted
Jun 18, 2026
Start date
Jun 18, 2026 (estimated)
Primary completion
Jul 16, 2026 (estimated)
Completion
Jan 16, 2027 (estimated)
Last update
Jun 18, 2026

Study contacts

Elif Develi, PhD
Contact
elifstn@yahoo.com
+90 555 593 62 93

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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