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Clinical Trials/ISRCTN62945682
ISRCTN62945682
Completed
未知

Comparison of the effects of thermal stimulation and transcutaneous electrical nerve stimulation on upper extremity sensory and motor function in individuals with acute stroke: a randomized controlled pilot study

Kaohsiung Medical University0 sites27 target enrollmentMay 25, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
intervention for individuals with acute stroke
Sponsor
Kaohsiung Medical University
Enrollment
27
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 25, 2022
End Date
January 27, 2016
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged 20 years or older
  • 2\. Have a stroke for the first time
  • 3\. Have been examined by a physician, and were approved to receive rehabilitation treatment
  • 4\. Hospitalized during the acute phase
  • 5\. Hemiparesis
  • 6\. Do not have obvious cognitive impairments
  • 7\. Can independently maintain a sitting posture for at least 30 min

Exclusion Criteria

  • 1\. Have skin conditions or injuries (e.g., wounds) on upper limbs or have other contraindications for electrotherapy or TS (e.g., a malignant tumor)
  • 2\. Have a language disorder (e.g., aphasia) and is therefore unable to communicate or comply with instructions
  • 3\. Have other orthopedic conditions (e.g., severe arthritis) or nerve damage (e.g., peripheral nerve injury) affecting movement in their upper limbs
  • 4\. Have diabetes or complete sensory impairment not caused by stroke (e.g., peripheral vascular disease or neuropathy)
  • 5\. Have developed neurological disorders during the experiment period or other conditions that may affect the study results
  • 6\. Have uncontrolled hypertension, unstable angina, a history of myocardial infarction or epilepsy (excepting febrile seizures) in the past 3 months, or a pacemaker
  • 7\. Have participated in other rehabilitation trials or drug trials
  • 8\. Unable to cooperate with the researchers because of cognitive or personal reasons or refused to provide written informed consent

Outcomes

Primary Outcomes

Not specified

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