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Long Term Effects of Soft Splints on Stroke Patients and Patients With Disorders of Consciousness

NCT03008486 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2019-09-25

No results posted yet for this study

Summary

The purpose of this study is to assess the effects on upper limb spasticity of soft splints worn during three weeks three hours a day by patients with stroke or disorders of consciousness.

Conditions

  • Brain Injuries
  • Disorder of Consciousness
  • Stroke
  • Spasticity as Sequela of Stroke
  • Contracture
  • Hypertonic Disorder
  • Central Nervous System Diseases
  • Pathologic Processes
  • Craniocerebral Trauma
  • Trauma, Nervous System
  • Neurocognitive Disorders

Interventions

DEVICE

Real soft splint (6 cm)

DEVICE

Placebo soft splint (1 cm)

Sponsors & Collaborators

  • Centre Hospitalier Universitaire UCLouvain Namur

    collaborator OTHER

  • Géraldine Martens

    lead OTHER

Principal Investigators

  • Nicolas Lejeune · Centre Hospitalier Neurologique William Lennox

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2019-01-31
Completion
2019-06-30

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03008486 on ClinicalTrials.gov