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Clinical Trials/NCT06708884
NCT06708884
Not Yet Recruiting
N/A

Is Telerehabilitation a Good Alternative to Face-to-Face Rehabilitation Beyond Clinical Walls in Recovery After Total Hip Arthroplasty

Burdur Mehmet Akif Ersoy University1 site in 1 country36 target enrollmentDecember 15, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Total Hip Arthroplasty (THA)
Sponsor
Burdur Mehmet Akif Ersoy University
Enrollment
36
Locations
1
Primary Endpoint
Functional level
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to learn if telerehabilitation in patients who had undergone total hip arthroplasty. The main questions it aims to answer are:

  • Does telerehabilitation improve the functional level of the participants?
  • Does telerehabilitation improve the locomotor performance of the participants? Researchers will compare telerehabilitation to face to face rehabilitation (traditional rehabilitation programme) to see if telerehabilitation works in total hip arthroplasty recovery.

Participants will:

  • Attend physiotherapy and rehabilitation sessions supervised by a physiotherapist 2 days a week for 8 weeks.
  • Participate in assessments (before surgery and at 6 weeks and 12 weeks after surgery).
Registry
clinicaltrials.gov
Start Date
December 15, 2024
End Date
April 15, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Burdur Mehmet Akif Ersoy University
Responsible Party
Principal Investigator
Principal Investigator

Akın Süzer

Principal Investigator

Burdur Mehmet Akif Ersoy University

Eligibility Criteria

Inclusion Criteria

  • Having hip arthroplasty surgery
  • To be able to understand verbal and written information
  • No cognitive impairment
  • To be able to speak and understand Turkish

Exclusion Criteria

  • Having a neurological disease
  • Having a psychiatric disorder
  • Visual or hearing loss that cannot be corrected with any assistive device

Outcomes

Primary Outcomes

Functional level

Time Frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.

Functional level was assessed using the Western Ontario McMaster University Osteoarthritis Index. Western Ontario and McMaster Universities Osteoarthritis Index consists of 24 questions and 3 subcategories (pain, stiffness and physical function). Pain is evaluated with 5 questions, stiffness with 2 questions and physical function with 17 questions. Each question in the Index is scored from 0 (none) to 4 (very severe, very difficult). The total score can be a minimum of 0 and a maximum of 100. In addition, each subcategory can also be evaluated on its own. A higher score on the Index indicates more symptoms and physical disability.

Secondary Outcomes

  • Pain intensity(Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.)
  • Quality of life(Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.)
  • Locomotor performance(Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.)
  • Lower extremity muscle strength(Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.)
  • Hip Joint Range of Motion (ROM)(Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.)

Study Sites (1)

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