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Clinical Trials/ACTRN12613001225707
ACTRN12613001225707
Completed
未知

Telerehabilitation versus standard care for management of pressure ulcers in people with spinal cord injury in India- a 12-week TREPUS randomized controlled trial.

John Walsh Centre for Rehabilitation Research, The University of Sydney0 sites120 target enrollmentNovember 7, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Pressure ulcers in people with spinal cord injury.
Sponsor
John Walsh Centre for Rehabilitation Research, The University of Sydney
Enrollment
120
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 7, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
John Walsh Centre for Rehabilitation Research, The University of Sydney

Eligibility Criteria

Inclusion Criteria

  • Participants will be included if they:
  • i. are 18 years of age or over, and willing to provide signed informed consent.
  • ii. have a documented diagnosis of complete or incomplete spinal cord injury:
  • iia. due to traumatic or non\-traumatic cause.
  • iib. of more than 6 months duration.
  • iii.have at least one pressure ulcer secondary to SCI on sacrum, ischial tuberosity or trochanter.
  • iv. are living in the National Capital Region or are able to return to the Indian Spinal Injuries Centre for assessment.
  • v. are able to speak sufficient Hindi to allow them to participate in the study without the assistance of a translator.
  • vi. have access to a mobile phone and will be able to comply with regular phone interviews as specified by the protocol.
  • vii. are likely to comply with the study schedule and assessments as specified by the protocol.

Exclusion Criteria

  • Participants will be excluded if they:
  • i. have been advised of the possibility of requiring surgery within the next 12 weeks.
  • ii. are not willing or able to be contacted on a mobile phone.
  • iii. have any cognitive or verbal impairment.
  • iv. have a clinically significant or unstable medical condition including psychiatric, behavioural or terminal illness that would compromise participation in the study.

Outcomes

Primary Outcomes

Not specified

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