Exploring Lived Experiences of Families of Children With Spinal Muscular Atrophy(SMA) Type 1 Regarding Feeding and Communication
Exploring Lived Experiences of Families of Children With Spinal Muscular Atrophy(SMA) Type 1 Regarding Feeding and Communication
Not yet recruiting · NCT07596277 · Registry updated 2026-06-02Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Exploring Lived Experiences of Families of Children With Spinal Muscular Atrophy(SMA) Type 1 Regarding Feeding and Communication | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, Digestive System Diseases, Pharyngeal Diseases, Spinal Muscular Atrophies of Childhood, Spinal Muscular Atrophy Type I, central nervous system disorder, digestive system disorder, esophageal disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, otorhinolaryngologic disease, spinal cord disorder, spinal muscular atrophy | Not yet recruiting | Not stated | 2026-06-02 | NCT07596277 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Guy's and St Thomas' NHS Foundation Trust | 118 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| GSTT Evelina Neurosciences | London | United Kingdom | 1 |