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Clinical Trials/ACTRN12618001448235
ACTRN12618001448235
Active, not recruiting
未知

The PATHway Trial: Participatory health through behavioural engagement and disruptive digital technology for post-operative rehabilitation of lumbar decompression and total knee replacement.

The University of Sydney0 sites167 target enrollmentAugust 28, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
The University of Sydney
Enrollment
167
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 28, 2018
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Ability and willingness to participate in the study
  • 2\. Familiarity with the use of the Internet and smart devices
  • 3\. Ownership of a smartphone
  • 4\. Participants must have at least functional English to be able to understand the study procedures, complete the questionnaires, communicate during the health coaching sessions and consent to participate in the study
  • 5\. aged 18 years or older, male or female
  • 6\. Admission to one of the study sites for rehabilitation following total knee replacement or lumbar decompression with or without fusion

Exclusion Criteria

  • 1\. Known or suspected serious spinal pathology (fracture, metastatic, inflammatory or infective diseases, widespread neurological disorder).
  • 2\. Any clinically significant acute or ongoing chronic medical conditions (e.g., uncontrolled diabetes) that could compromise patient safety, limit the patient’s ability to complete the study, and/or compromise the objectives of the study.
  • 3\. Patients undergoing bilateral knee replacement.
  • 4\. Patients undergoing revision for a previous total knee replacement or spinal surgery.
  • 5\. Participation in another clinical trial and/or treatment received with any investigational agent within 30 days before enrolment.
  • 6\. Current use of any intervention component (activity tracker, exercises app or health coaching) and unwillingness to stop using it for the duration of the study.
  • 7\. Spinal surgery beyond two spine levels.
  • 8\. Participants beyond 45 days post\-op.

Outcomes

Primary Outcomes

Not specified

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