- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07656961
Ayres Sensory Integration Test Evaluation Results and Neurodevelopmentally Focused Counseling in Children With Neurodevelopmental Problems
Aperçu de l'étude
Statut
Les conditions
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Elif Develi, PhD
- Numéro de téléphone: +90 555 593 62 93
- E-mail: elifstn@yahoo.com
Lieux d'étude
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Ataşehir
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Istanbul, Ataşehir, Turquie (Türkiye), 34755
- Yeditepe University
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
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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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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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The Evaluation of Ayres Sensory Integration (EASI)
Délai: 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
Délai: 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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Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 125 (Norgine)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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