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NCT06864767
Impact of Motor and Oral Motor Function on Quality of Life in Children With SMA
trial testing Neuro-sensory Motor Developmental Assessment in Spinal Muscular Atrophy Type I in 23 participants. Completed in 30 August 2024.
15 June 2024
Quick facts
| Lead sponsor | Zeynep HOŞBAY |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 23 |
| Start date | 30 May 2024 |
| Primary completion | 15 June 2024 |
| Estimated completion | 30 August 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Neuro-sensory Motor Developmental Assessment
- Functional Oral Intake Scale
- Behavioral Pediatrics Feeding Assessment Scale
- Pediatric Quality of Life Inventory
Conditions studied
- Spinal Muscular Atrophy Type I — all drugs for Spinal Muscular Atrophy Type I →
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.
Verify or expand the search:
- PubMed search for NCT06864767
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Spinal Muscular Atrophy Type I
Currently open trials in the same condition.
- NCT04042025 — Long-term Follow-up Study of Patients Receiving Onasemnogene Abeparvovec-xioi · Phase 3 · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06864767 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Zeynep HOŞBAY
- Last refreshed: 7 March 2025
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