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Clinical Trials/ISRCTN99941302
ISRCTN99941302
Active, not recruiting
未知

Time is of the essence: the impact of early initiated upper-body aerobic exercise on cardiovascular health following spinal cord injury

niversity of Birmingham0 sites42 target enrollmentJune 2, 2023

Overview

Phase
未知
Intervention
Not specified
Conditions
Sub-acute spinal cord injury
Sponsor
niversity of Birmingham
Enrollment
42
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 2, 2023
End Date
May 17, 2026
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • For patients:
  • 1\. At least 18 years old
  • 2\. Males and females
  • 3\. Have had a motor\-complete SCI (AIS A or B) at the cervical or thoracic level (between C5 \- T12\) within 3 months.
  • 4\. Are cleared by their medical team to begin standard of care rehabilitation
  • 5\. Can move their shoulders and arms voluntarily to operate the arm\-crank ergometer
  • 6\. Compliance: understands and is willing, able and likely to comply with all study procedures and restrictions.
  • 7\. Consent: demonstrates an understanding of the study and willingness to participate, as evidenced by voluntary written informed consent
  • 1\. Currently be a member of the medical team supporting sub\-acute spinal cord injured patients at MCSI
  • 2\. Be at least 18 years old

Exclusion Criteria

  • For patients:
  • 1\. Participants are pregnant (women who become pregnant will be advised to notify clinical staff, and upon notification, will be withdrawn from the trial)
  • 2\. Participants are under the age of 18 years
  • 3\. Participants have an SCI lower than the T12 neurological level
  • 4\. Participants have an SCI above the C5 neurological level, intubation, a trachea in situ or require mechanical ventilation
  • 5\. Have medical complications from the injury that in the opinion of the healthcare team would restrict or prevent the participation in exercise rehabilitation, pose an undue personal risk or introduce bias into the trial
  • 6\. Co\-occurring traumatic brain injury or cognitive impairment that either impacts the ability to follow study instructions and/or provide informed consent
  • 7\. Unable to provide full informed consent

Outcomes

Primary Outcomes

Not specified

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