Exercise: exercise programme will be implemented via telerehabilitation
Exercise: exercise programme will be implemented via face-to-face
Study 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).
Eligibility
Sex
ALL
Min age
50 Years
Max age
80 Years
Healthy volunteers
No
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
Primary outcome measure(s)
Functional level — 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.
Trial sites (1)
Facility
City
Region
Status
Burdur Mehmet Akif Ersoy University
Burdur
Turkey (Türkiye)
More Burdur Mehmet Akif Ersoy University trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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