ExSpAnD SMA

  • Research type

    Research Study

  • Full title

    Exploring bulbar function, Speech And communication Development in SMA type 1 (ExSpAnD SMA)

  • IRAS ID

    298924

  • Contact name

    Giovanni Baranello

  • Contact email

    g.baranello@ucl.ac.uk

  • Sponsor organisation

    UCL - Great Ormond Street Institute of Child Health

  • Clinicaltrials.gov Identifier

    NCT05954455

  • Clinicaltrials.gov Identifier

    Z6364106/2023/06/153 health research , UCL Data Protection Office

  • Duration of Study in the UK

    3 years, 0 months, 0 days

  • Research summary

    5q-spinal muscular atrophy (5q-SMA) is a rare, autosomal recessive neuromuscular disease characterized by degeneration of motor neurons in the spinal cord and lower brainstem with progressive muscle atrophy, weakness, and paralysis. The incidence is 1 in 7-10,000 live births. 5q-SMA presents a wide range of phenotypes that are classified into five clinical groups depending on age of onset and maximum motor milestone achieved. SMA type 1 presents shortly after birth and before six months of age with inability to achieve independent sitting and limited life expectancy due to respiratory complications (high mortality rate by 2 years of age). In addition to the severe gross-motor and respiratory impairment, bulbar weakness and dysfunction represent an obstacle to the development of verbal skills in these patients. To date, very little is known about these functions in children with SMA 1. With the increasing number of long-term SMA 1 survivors worldwide thanks to the availability of new pharmacological treatments, it has become obvious that treated children show new phenotypes, presenting changes not only in motor and respiratory function, but also in other domains, including bulbar function, speech and communication development. We aim to investigate the evolution of bulbar function and speech/communication development in children with SMA type 1 treated with approved disease-modifying therapies through validate scales and questionnaires for the paediatric population. Additional neurophysiological and neuroimaging studies will be offered on an optional basis to further investigate the underlying brain electrical activity, and brain structural and functional organization. The information gathered would promote the definition of additional outcome measures capturing improvement at these levels. A better understanding of the development of these areas would help to plan SMA 1-tailored supportive programs provided by speech and language therapists, thus enhancing the current recommendations for management in SMA.

  • REC name

    London - Harrow Research Ethics Committee

  • REC reference

    23/PR/0914

  • Date of REC Opinion

    2 Nov 2023

  • REC opinion

    Further Information Favourable Opinion