Effects Of A Home Based Exercise Program Following Total Hip Arthroplasty

February 15, 2024 updated by: Halic University

Investigation Of The Effects Of A Home Based Exercise Program Under Physiotherapist Supervision Following Total Hip Arthroplasty And Comparison With The Control Group

The aim of this study is to examine the effects of home-based exercise on pain-related factors, postural control and early functional parameters in individuals undergoing total hip arthroplasty. Forty-four individuals with hip osteoarthritis were included in current study. Individuals were randomized as study group (n=23) and control group (n=21) by drawing lots. Individuals in the study group were followed up with a personalized home-based exercise program for 6 weeks. Individuals in the control group were followed up with an exercise training brochure. The exercise program of the individuals in the study group was checked at two-week intervals and adjustments were made in the exercise program. All individuals were evaluated before the operation, 2 weeks after the operation, and 12 weeks after the operation, and their data were recorded. Range of motion was measured with an inclinometer, muscle strength was measured with a hand dynamometer, joint position sense was measured with a target angle test, pain was measured with a visual pain scale, leg length was measured with a tape measure, and finally, the Q angle was measured with a goniometer. In addition to these,Tampa kinesiophobia scale, Oxford hip score and international physical activity scale were used. Timed up-and-go test was used to evaluate functional performance. Foursquare step test was used to evaluate balance, and finally, tetrax posturography device was used to evaluate postural control.

Study Overview

Status

Active, not recruiting

Conditions

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

Interventional

Enrollment (Actual)

48

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Yeditepe Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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.
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:
  • educational supervised exercises
Other: Control group
After total hip arthroplasty, participants who take an educational booklet (about exercise program) at hospital stay
Individuals in the control group were followed up with an exercise training brochure.
Other Names:
  • educational booklet

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
OXFORD HİP SCORE
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
TAMPA SCALE FOR KINESİOPHOBİA
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.

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.
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.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
FOUR SQUARE STEP TEST
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
It is a measurement of dynamic standing balance.Performance time is calculated for each individual. Prolonged performances indicate an absence of equilibrium.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
Assessment of Postural Control
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MEASURİNG LEG LENGTH DİSCREPANCY
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
Q ANGLE
Time Frame: Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.
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.
Prior to surgery, two weeks following surgery, and twelve weeks following surgery, the same measurements will be taken.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 10, 2023

Primary Completion (Actual)

April 30, 2023

Study Completion (Estimated)

June 30, 2024

Study Registration Dates

First Submitted

February 2, 2024

First Submitted That Met QC Criteria

February 15, 2024

First Posted (Estimated)

February 23, 2024

Study Record Updates

Last Update Posted (Estimated)

February 23, 2024

Last Update Submitted That Met QC Criteria

February 15, 2024

Last Verified

February 1, 2024

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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