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Study of Feasibility to Reliably Measure Functional Abilities' Changes in Nonambulant Neuromuscular Patients Without Trial Site Visiting

C

Charitable Foundation Children with Spinal Muscular Atrophy

Status

Withdrawn

Conditions

Neuromuscular Disorders
Spinal Muscular Atrophy

Treatments

Other: Direct current stimulation of cervical spinal cord

Study type

Interventional

Funder types

Other

Identifiers

NCT02235090
CSMA-INPN-1

Details and patient eligibility

About

Clinical trials organization in several neuromuscular disorders (NMD) has some specific issues. Nonambulant status and difficulties with transportation are among them. Moreover a lot of patients with NMD have so poor condition that even short transportation is able to worse it. Such situation forces researchers to limit a region of recruitment for clinical trials and to exclude from trials more severe subgroup of patients, which cause additional issues especially for rare diseases.

The purpose of this study is to prove hypothesis about possibility to reliably monitor patient condition remotely, without trial site visiting. Visit-free study design is potentially able to widen eligible patient population and to decrease patient dropout rate as well as burden of numerous assessments. Meanwhile assessment frequency could be increased enabling monitoring of short fluctuations in patients' condition.

Spinal muscular atrophy (SMA) is a rare neuromuscular condition to which all mentioned above issues are completely applicable. Direct current stimulation (DCS) of neural structures is well studied and safe intervention, however, its effects on SMA patients' strength and durability has not been reported for today. The investigators suppose that investigation of DCS action in SMA patient population is an adequate model for visit-free design feasibility, reliability and sensitivity evaluation.

Sex

All

Ages

5+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Signed informed consent
  • 5q SMA confirmed by molecular testing

Exclusion criteria

  • Need for ventilation
  • Hypersensitivity (pain or allergic reaction) to current stimulation

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

0 participants in 3 patient groups

Zero-strength of direct current stimulation
Sham Comparator group
Description:
Sham transdermal direct current stimulation of cervical spinal cord
Treatment:
Other: Direct current stimulation of cervical spinal cord
100 microamperes direct current stimulation
Experimental group
Description:
Transdermal direct current stimulation of cervical spinal cord
Treatment:
Other: Direct current stimulation of cervical spinal cord
1 milliampere direct current stimulation
Experimental group
Description:
Transdermal direct current stimulation of cervical spinal cord
Treatment:
Other: Direct current stimulation of cervical spinal cord

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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