Skip to main content
Clinical Trials/ISRCTN42991002
ISRCTN42991002
Completed
未知

pper limb Telerehabilitation using Brain-Controlled Functional Electrical Stimulation (Tele BCI-FES)

Sheffield Teaching Hospitals NHS Foundation Trust0 sites9 target enrollmentJanuary 6, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
pper limb stroke rehabilitation
Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Enrollment
9
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 6, 2022
End Date
December 1, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Age 18 years and above
  • 2\. Experienced an ischaemic or haemorrhagic stroke over 6 months ago
  • 3\. Arm weakness interfering with activities of daily living
  • 4\. Fugl\-Meyer score of upper limb \<45
  • 5\. Caregiver is willing to assist with trial by helping to deliver intervention
  • 6\. Cognitive and language abilities to understand and participate in the study protocol
  • 7\. Can maintain sitting with or without support for 1 hour continuously
  • 8\. Able to give consent and understand instructions

Exclusion Criteria

  • 1\. Cognitive impairment that would interfere with their ability to comply with the experimental protocol or provide informed consent
  • 2\. Dermatological, rheumatologic or orthopaedic illnesses of the affected arm interfering with movement of the elbow
  • 3\. Pre\-existing severe systemic disorders like cardiovascular disease; active cancer or renal disease; end\-stage pulmonary or cardiovascular disease; psychiatric illness including severe alcohol or drug abuse
  • 4\. Inability to perform the baseline assessments
  • 5\. Severe tactile hypersensitivity
  • 6\. Participation in other, upper limb rehabilitation studies
  • 7\. Within 12 weeks of receiving Botulinum toxin injections
  • 8\. Uncontrolled epilepsy
  • 9\. Pacemaker or any other implanted devices
  • 10\. Pregnancy

Outcomes

Primary Outcomes

Not specified

Similar Trials