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NCT06864767

Impact of Motor and Oral Motor Function on Quality of Life in Children With SMA

Completed Last updated 7 March 2025
What this trial tests

trial testing Neuro-sensory Motor Developmental Assessment in Spinal Muscular Atrophy Type I in 23 participants. Completed in 30 August 2024.

Timeline
30 May 2024
Primary endpoint
15 June 2024
30 August 2024

Quick facts

Lead sponsorZeynep HOŞBAY
StatusCompleted
Study typeOBSERVATIONAL
Enrollment23
Start date30 May 2024
Primary completion15 June 2024
Estimated completion30 August 2024
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Zeynep HOŞBAY

Who can join

Adults 2 to 4, any sex, with Spinal Muscular Atrophy Type I. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to investigate the impact of motor and oral motor functions on the quality of life in children aged 2-4 years diagnosed with Spinal Muscular Atrophy (SMA) Type I. In the study, the Neuro-Sensory-Motor Developmental Assessment (NSMDA) was used to evaluate motor functions, the Functional Oral Intake Scale (FOIS) to assess oral motor function, the Behavioral Pediatric Feeding Assessment Scale (BPFAS) to evaluate children's attitudes towards feeding, and the Pediatric Quality of Life Inventory (PedsQL) Neuromuscular Module to assess quality of life.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Spinal Muscular Atrophy Type I

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06864767.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing