- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07656961
Ayres Sensory Integration Test Evaluation Results and Neurodevelopmentally Focused Counseling in Children With Neurodevelopmental Problems
Studieoversigt
Status
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Elif Develi, PhD
- Telefonnummer: +90 555 593 62 93
- E-mail: elifstn@yahoo.com
Studiesteder
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Ataşehir
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Istanbul, Ataşehir, Tyrkiet (Türkiye), 34755
- Yeditepe University
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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:
- Being under 3 years of age or over 12 years of age
- Having no conditions that fall outside normal developmental parameters
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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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.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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The Evaluation of Ayres Sensory Integration (EASI)
Tidsramme: 4 Weeks
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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.
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4 Weeks
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Pediatric Sensory Profile
Tidsramme: 4 weeks
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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.
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4 weeks
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 125 (Norgine)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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