About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
Having hip arthroplasty surgery
To be able to understand verbal and written information
No cognitive impairment
To be able to speak and understand Turkish
Disqualifiers
Having a neurological disease
Having a psychiatric disorder
Visual or hearing loss that cannot be corrected with any assistive device
Trial design
Parallel
Treatments tested in this trial
Exercise
Other interventionexercise programme will be implemented via telerehabilitation
Exercise
Other interventionexercise programme will be implemented via face-to-face
Treatment groups
Trial outcomes
Primary outcomes
Functional level
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
Pain intensity was assessed using the pain subcategory of Western Ontario McMaster University Osteoarthritis Index and the Visual Analog Scale. There are 5 questions in the pain subcategory of the Western Ontario and McMaster Universities Osteoarthritis Index. Each question in the Index is scored from 0 (none) to 4 (very severe, very difficult). The pain score can be a minimum of 0 and a maximum of 20. A higher pain score indicates more pain. Visual Analog Scale consists of a horizontal 10 cm straight line. When viewed from left to right, there is a value of 0 at the beginning and 10 at the end of the line. The 0 point of the line indicates no pain and the 10 point indicates the most severe pain felt in life.
Quality of life
Quality of life will be assessed with the EQ-5D General Quality of Life Questionnaire. The first part of the questionnaire consists of questions related to five different areas of health, including mobility, personal care, usual activities, pain/discomfort, and anxiety/depression. Each question is rated on a three-point scale as 'no problem, some problem and major problem'. Therefore, the questionnaire generates 243 different results. As a result of the scoring, a score between -0.59 and 1 is obtained and 0 indicates death, 1 indicates full health, minus values indicate unconsciousness, etc. The second part of the questionnaire shows the score that the person gives to the health status by marking on a vertical ruler or a thermometer-like visual analogue scale between 0 and 100. A score of 100 indicates the healthiest state.
Locomotor performance
Locomotor performance was assessed with the stair climb test. Stair Climb Test: The time taken to ascend and then descend a 9-step staircase was recorded as the patient's score.
Lower extremity muscle strength
Lower extremity muscle strength will be assessed with the a hand dynamometer. Hand Dynamometer: Hip muscles (flexors, extensors, abductors and adductors) and knee extensors will be evaluated using a hand dynamometer (Commander Muscle Tester, JTech, USA). 3 consecutive maximum isometric contraction measurements at 1 minute intervals will be averaged.
Sponsors and contacts
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Burdur Mehmet Akif Ersoy University
Lead sponsor
Pamukkale University
Collaborator
This trial is not recruiting at the moment. You can still explore other options: