- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06274866
Effects Of A Home Based Exercise Program Following Total Hip Arthroplasty
Investigation Of The Effects Of A Home Based Exercise Program Under Physiotherapist Supervision Following Total Hip Arthroplasty And Comparison With The Control Group
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of this study was to examine the patients who underwent Total Hip Arthroplasty surgery with the diagnosis of hip osteoarthritis.
Home-based exercise program given individually under the control of a physiotherapist is effective in reducing pain.
related factors (joint range of motion, muscle strength, kinesiophobia, physical activity), To investigate its effect on functional status, balance and postural control.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey
- Yeditepe Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having surgery with a diagnosis of osteoarthritis
- Cases have unilateral hip osteoarthritis
- Not having received physical therapy in the 6 months before the surgery
- Total hip arthroplasty surgery should only be performed on posterior or posterolateral done with initiative
Exclusion Criteria:
- Presence of Dementia, Neurological Deficit
- Having other diseases that may affect balance (vertigo, previous CVO, neuropathy, epilepsy)
- Being on medication that may affect balance (antidepressants, antiepileptics, antipsychotics)
- Individuals who use alcohol heavily
- End stage organ failure
- Cancer patients under active treatment (except those in remission
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Study Group
After total hip arthroplasty, participants who take supervised home based exercised program which consists especially early weight bearing hip specific mobilization and strengthening exercises.
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Study group were followed up with a personalized home-based exercise program for 6 weeks.
IThe exercise program of the individuals in the study group was checked at two-week intervals and adjustments were made in the exercise program
Other Names:
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Other: Control group
After total hip arthroplasty, participants who take an educational booklet (about exercise program) at hospital stay
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Individuals in the control group were followed up with an exercise training brochure.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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OXFORD HİP SCORE
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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The Oxford Hip Score consists of 12 questions asking patients to describe their hip pain and function during the past 4 weeks.
Each item uses a 5-point response scale with values from 0 to 4. An overall score is created by summing the responses to each of the 12 questions.
The total score can range from 0 to 48 (most recent scoring system), where 0 is the worst possible score, indicating severe hip problems, and 48 is the best score, suggesting excellent hip function
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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TAMPA SCALE FOR KINESİOPHOBİA
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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It is a scale consisting of 17 questions created to measure fear of injury. The scale includes injury/re-injury and fear-avoidance parameters in work-related activities.A 4-point Likert scoring on the scale (I strongly disagree 1, I disagree 2, I agree 3, I completely agree 4) is used. Individuals receive a total score between 17-68. A high score on the scale indicates that the person has a high level of kinesiophobia. Scores over 37 points are interpreted as high kinesiophobia. |
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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İNTERNATİONAL PHYSİCAL ACTİVİTY QUESTİONAİRE (SHORT FORM)
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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The short form records the activity of four intensity levels: 1) vigorous-intensity activity such as aerobics, 2) moderate-intensity activity such as leisure cycling, 3) walking, and 4) sitting.
The original authors recommended the "last 7 day recall" version of the questionaire for physical activity surveillance.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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JOİNT POSİTİON SENSE ERROR TEST
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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The range of motion in the hip flexion direction is determined to be tested as active movement and passive movement in the 30 ˚, 60 ˚ and 90 ˚ positions.
Movement deviations from specified angles are recorded along with the degree of deviation.
The joint position sense error increases with the amount of deviation from the anticipated angle.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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FOUR SQUARE STEP TEST
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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It is a measurement of dynamic standing balance.Performance time is calculated for each individual.
Prolonged performances indicate an absence of equilibrium.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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THE TİMED UP and GO TEST
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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The timed up and go test measures in seconds the time it takes a subject to rise from a chair, walk a distance of 3 meters, turn, walk back to the chair and sit down.
This test has been used to examine balance, gait speed, and functional ability that would be required for the performance of basic activities of daily living in older people.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Assessment of Hip Muscle Strength
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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A microFET®2 (Digital Hand-held Dynamometer, Hoggan Scientific, LLC; Salt Lake City, Utah) Hand-Held Dynamometer is going to used to measure muscle strength.
Using the break test method, which reveals isometric muscle contraction during the muscle test, force is applied in the opposite direction until a joint movement occurred exceeding the maximum power applied with the dynamometer.
The strength of the healthy and osteoarthritic hip muscles are evaluated with the patient in supine position.
The measurements are recorded as Newton (N) units.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Assessment of Hip Joint Range of Motion
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Individuals' hip joint range of motion will be evaluated using the Baseline Bubble® Inclinometer.
Hip flexion and abduction active range of motion will be evaluated in the standing position, and hip rotations will be evaluated in the supine position.
Decreased hip joint range of motion is a clinical precursor of hip osteoarthritis, characterized by pain and loss of function.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Assessment of Postural Control
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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To evaluate postural control, measurements will be made with a software-based static posturography device (Tetrax®, Sunlight Medical Ltd).
Tetrax® consists of four independent platforms that measure vertical pressure changes from both toes and both heels, and a computer software that combines the digital data from this platform.
The system can digitally record data from four different measurement platforms in a certain period of time and document it as visual and numerical values.
While measuring, individuals place their bare feet on the platforms and stand comfortably in a quiet environment.
Individuals hold their head and eyes open and closed.
It is evaluated in 8 different positions using neck rotations.
The software evaluates postural control by generating a stability index with a numerical value from all measurements.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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MEASURİNG LEG LENGTH DİSCREPANCY
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Leg length will be recorded in cm by measuring the distance between the major trochanter and the medial malleolus with a 6 mm tape measure.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Q ANGLE
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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The patients are placed in the supine position, and the axis between the tibial tubercle and the midpoint of the patella is measured along with the axis between the spina iliaca anterior superior and the midpoint of the patella.
The angle value between these two axes is then recorded numerically.
Goniometers are used to take measurements.
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Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Davis AM, Perruccio AV, Ibrahim S, Hogg-Johnson S, Wong R, Streiner DL, Beaton DE, Cote P, Gignac MA, Flannery J, Schemitsch E, Mahomed NN, Badley EM. The trajectory of recovery and the inter-relationships of symptoms, activity and participation in the first year following total hip and knee replacement. Osteoarthritis Cartilage. 2011 Dec;19(12):1413-21. doi: 10.1016/j.joca.2011.08.007. Epub 2011 Aug 18.
- Pop T, Szymczyk D, Majewska J, Bejer A, Baran J, Bielecki A, Rusek W. The Assessment of Static Balance in Patients after Total Hip Replacement in the Period of 2-3 Years after Surgery. Biomed Res Int. 2018 Jan 4;2018:3707254. doi: 10.1155/2018/3707254. eCollection 2018.
- Ometti M, Brambilla L, Gatti R, Tettamanti A, La Cava T, Pironti P, Fraschini G, Salini V. Capsulectomy vs capsulotomy in total hip arthroplasty. Clinical outcomes and proprioception evaluation: Study protocol for a randomized, controlled, double blinded trial. J Orthop. 2019 Sep 12;16(6):526-533. doi: 10.1016/j.jor.2019.09.020. eCollection 2019 Nov-Dec.
- Trudelle-Jackson E, Emerson R, Smith S. Outcomes of total hip arthroplasty: a study of patients one year postsurgery. J Orthop Sports Phys Ther. 2002 Jun;32(6):260-7. doi: 10.2519/jospt.2002.32.6.260.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- dsahinoglu
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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