Burdur Mehmet Akif Ersoy University
Burdur, 15100, Turkey (Türkiye)
NCT Number: NCT06708884
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).
Trial opening soon.
Get Notified50 year–80 year
All sexes
Interventional
Not applicable
Burdur, 15100, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
exercise programme will be implemented via telerehabilitation
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.
Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.
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.
Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.
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.
Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.
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.
Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.
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.
Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.
Range of Motion (ROM) will be evaluated by goniometric measurement.
Contact information is provided by the study sponsor or research team.
Burdur Mehmet Akif Ersoy University
Other
Is Telerehabilitation a Good Alternative to Face-to-Face Rehabilitation Beyond Clinical Walls in Recovery After Total Hip Arthroplasty
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07696650
Arthritis, Behavior
Vancouver, British Columbia, Canada
View Trial DetailsNCT07683663
Acute Pain, Arthritis
Izmir, Balçova, Turkey (Türkiye)
View Trial DetailsNCT07630896
Arthritis, Joint Diseases
New York, United States
View Trial DetailsNCT07616895
Total Hip Arthroplasty (THA)
View Trial Details