Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty.

Sponsor
Dokuz Eylul University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03421938
Collaborator
(none)
0
1
2
5.3
0

Study Details

Study Description

Brief Summary

This study is planned for investigating effect of downhill-uphill walking exercises on functional level and muscle strength in patients with knee arthroplasty. Patients who have had primary knee arthroplasty and has gone 3 months after surgery will be included in this study. The patients will be divided into two groups by randomization. Totally, 22 patients will be included in this study. Every patients will have same standart post-operative rehabilitation programme. In addition,group 1 will have downhill walking exercises with %10 slope; group 2 uphill walking exercises on the treadmill with %10 slope. Assessments will be made before and after treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: Walking Exercise
N/A

Detailed Description

This study is planned for investigating effect of downhill-uphill walking exercises on functional level and muscle strength in patients with knee arthroplasty. Patients who have had primary knee arthroplasty and has gone 3 months after surgery will be included in this study. The patients will be divided into two groups by randomization. Totally, 22 patients will be included in this study. Every patients will have same standart post-operative rehabilitation programme. Assessments will be made before and after treatment. Rehabilitation programme after knee arthroplasty has included muscle strength and endurance, balance and proprioceptive sensation, increasing functional level and providing independence in daily life activities.For this purpose, a standard physiotherapy program will be implemented in accordance with the goals and objectives stated for all patients. In addition,group 1 will have downhill walking exercises with %10 slope; group 2 uphill walking exercises on the treadmill with %10 slope. It takes 30 minutes for one session.

Exercise intensity was measured before treatment; will be determined using the Karvonen formula depending on the heart rate. Walking intensity during exercise; 55% of the maximum heart rate will be determined at the beginning of the treatment and 85% towards the end of the treatment. Walking exercise on the treadmill will be performed in conjunction with a qualified physiotherapist in this area for 4 weeks(3 session in 1 week).

Within the scope of the assessments, patients' pain levels will be determined using the Numeric Pain Scale (NAS). For the knee joint, the normal range of motion will be determined by universal goniometer. For the determination of functional level, Iowa functional activity scale, Iowa ambulatory speed scale and Hospital For Special Surgery (HSS) knee scoring, 10-meter walking speed, Timed Up and Go (TUG) test, SF-12(12-Item Short Form Survey) quality of life scale will be used. Hand dynamometer will be used to evaluate muscle strength.These assessments will be made before and after treatment.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Investigation of the Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty.
Actual Study Start Date :
Oct 11, 2017
Anticipated Primary Completion Date :
Mar 20, 2018
Anticipated Study Completion Date :
Mar 20, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1 (Downhill Exercise Group)

This group will have downhill walking exercises with %10 slope.

Other: Walking Exercise
Group 1 will have downhill walking exercises with %10 slope; group 2 uphill walking exercises on the treadmill with %10 slope..

Experimental: Group 2 ( Uphill Exercise Group)

This group will have uphill walking exercises on the treadmill with %10 slope.

Other: Walking Exercise
Group 1 will have downhill walking exercises with %10 slope; group 2 uphill walking exercises on the treadmill with %10 slope..

Outcome Measures

Primary Outcome Measures

  1. Change of Iowa Level of Assistance Scale [Change from Baseline Patient's Functional Level at 4 weeks]

    This test assesses the patient's ability to perform four functional activities, namely, supine to sitting on the edge of the bed,sitting on the edge of the bed to standing, walking 4.57 metres. The scoring of these activities is done as independent 6 points, observational aid 5 points, minimum help 4 points, medium help 3 points, maximum help 2 points, fail 1 point and untest 0 points. Higher values represent a better outcome. Speed scoring is done by evaluating the walking speed at a distance of 13.4 meters (44 steps). 20 seconds (sec) and below are recorded as 0, 21-30 sec 1, 31-40 sec 2, 41-50 3, 51-60 sec 4, 61-70 sec 5 and 70 sec. Higher values represent a worse outcome

  2. Change of Hospital For Special Surgery Knee Score [Change from Baseline Patient's Functional Level at 4 weeks]

    Hospital for Special Surgery knee score. A scoring system evaluation of pain, mobility, range of motion and deforming of the knee giving 0-100 points

  3. Change of 10 meter walk speed test [Change from Baseline Patient's Functional Level at 4 weeks]

    Individual walks without assistance 10 meters and the time is measured for the intermediate 6 meters to allow for acceleration and deceleration, start timing when the toes of the leading foot crosses the 2-meter mark, stop timing when the toes of the leading foot crosses the 8-meter mark,assistive devices can be used but should be kept consistent and documented from test to test, if physical assistance is required to walk, this should not be performed can be performed at preferred walking speed or fastest speed possible documentation should include the speed tested (preferred vs. fast) collect three trials and calculate the average of the three trials

  4. Change of Timed Up and Go (TUG) [Change from Baseline Patient's Functional Level at 4 weeks]

    To determine fall risk and measure the progress of balance, sit to stand, and walking.The patient starts in a seated position. The patient stands up upon therapist's command walks 3 meters, turns around, walks back to the chair and sits down. The time stops when the patient is seated. The subject is allowed to use an assistive device.

Secondary Outcome Measures

  1. SF-12 [Change from Baseline SF-12 score Level at 4 weeks]

    SF-12 Health Survey is a shorter version of the SF-36 Health Survey that uses just 12 questions to measure functional health and well-being from the patient's point of view. The SF-12 is a practical, reliable and valid measure of physical and mental health and is particularly useful in large population health surveys or for applications that combine a generic and disease-specific health survey.

  2. Numeric Pain Scale [Change from Baseline Patient's Pain Level at 4 weeks]

    Severity of pain was rated by each patient marking their current level of pain on a 10cm visual analogue scale (VAS), where 0 represented no pain and 10 was the worst pain imaginable.Higher values represent a worse outcome.

  3. Range of Motion [Change from Baseline Patient's Range of Motion 4th week]

    Each patient's active (unassisted) range of knee extension and flexion will be measured, using a goniometer with the patient in the supine position.

  4. Muscle Strength [Change from Baseline Patient's Muscles Strengths at 4 weeks]

    Strength of knee muscles will be evaluated by hand-held dynamometer.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Preoperative diagnosis have to be knee osteoarthritis.

  • Patients with primary knee arthroplasty after 3 months surgery.

Exclusion Criteria:
  • BMI >40 kg/m2

  • Having orthopedic or neurologic disorders which cause walking disorders.

  • Revision total knee arthroplasty

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dokuz Eylul University İzmir Turkey 35340

Sponsors and Collaborators

  • Dokuz Eylul University

Investigators

  • Principal Investigator: Abdurrahman Nalbant, PT,MSc, Dokuz Eylul University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Abdurrahman Nalbant, Principal Investigator, Dokuz Eylul University
ClinicalTrials.gov Identifier:
NCT03421938
Other Study ID Numbers:
  • 3243-GOA
First Posted:
Feb 5, 2018
Last Update Posted:
Aug 23, 2021
Last Verified:
Aug 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Abdurrahman Nalbant, Principal Investigator, Dokuz Eylul University

Study Results

No Results Posted as of Aug 23, 2021