An Evaluation of the Graded Weight-bearing Exercise in Patients With Knee Osteoarthritis.
NCT ID: NCT05671146
Last Updated: 2023-10-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
45 participants
INTERVENTIONAL
2022-12-25
2023-07-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Aim: To evaluate the effect of a 6-weeks supervised graded weight-bearing exercise program on pain, function, proprioception, muscle strength in patients with knee osteoarthritis.
Material and Method: Thirty-six patients with chronic knee osteoarthritis with age ranging 40-60 years will be recruited from the physical therapy department and randomized into three groups. Group I: will receive graded weight-bearing exercise using the anti-gravity treadmill combined with open kinetic chain exercises. Group II will receive closed kinetic chain exercises with open kinetic chain exercises while group III will receive open kinetic chain exercises only i.e: stretching and strengthening exercises. The outcome measures will be pain, function, proprioception, and muscle strength.
Statistical analysis: To detect changes in the dependent variables within and between groups, one-way repeated measures Multivariate analysis will be applied. If there is a significant change within groups or between tests, the post hoc Bonferroni test will be used to detect the significance between each group and/or each level of measurement. The level of significance is p\<0.05 and confidence interval CI 95%.
Study Design: Single-blinded, randomised control trial.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Antigravity Treadmill in Knee Osteoarthritis (AGTreadmill)
NCT06347692
Effect of Retrowalking Program Versus Whole Body Vibration in Patients With Chronic Knee Osteoarthritis
NCT06110104
Different Levels of Blood Flow Restriction Versus Moderate Intensity Exercises in Patients with Knee Osteoarthritis
NCT06637124
Anti-gravity Treadmill Training in Patients With Knee Osteoarthritis
NCT05319964
Positive Pressure Treadmill Walking for Individuals With Knee Pathology
NCT04747444
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Study setting: The current study will be held at the laboratory at Umm Al-Qura University, Faculty of Applied Medical Sciences, Makkah, Saudi Arabia Recruitment and study population Patients will be recruited from the physical therapy outpatient clinic, Umm Al-Qura university medical centre, and other physical therapy outpatient clinic in Makkah.
Intervention group:
The intervention will be constructed based on recent clinical exercise guidelines for people with knee osteoarthritis. These guidelines mainly recommend weight-bearing exercises, progressive resistance training for lower limb major muscle groups, and aerobic exercise. The exercise regimen will be applied at two sessions per week for six weeks. The intervention is designed as the group I will perform progressive weight-bearing using an anti-gravity treadmill, the loading starts with patient tolerance - pain-free range and increases gradually, combined with open kinetic chain exercises. Group II will perform closed kinetic chain exercises with open kinetic chain exercises. Most of the exercises in these groups will be achieved in a weight-bearing position, with or without support, besides other exercises to improve knee flexors and extensors strength. An experienced physiotherapist will observe the intervention. Participants who have a higher risk of falling, restricted weight-bearing activities, or movement during training and activities will be given extra attention to avoid injuries. The physiotherapists will be trained to deliver the weight-bearing exercise program and ensure that participants have access to support devices. The session will last one hour and be repeated twice a week for six weeks. Participants' customizing, appropriate dosage, and progression of the exercises will be the responsibility of the physiotherapist supervising the exercise session. The exercise regimen will begin with a 10-minute warm-up that includes stretching, flexibility, and dynamic balance exercises. The warm-up will be followed by a graded weight-bearing exercise for group I and a closed kinetic chain exercise for group II with a short break for 30 seconds. Each session will end with 10 min cooling down and stretching. Participants are encouraged to report any significant side effects from the exercise, such as muscular soreness, joint tenderness, or increased pain level.
Control group:
Participants assigned to the control group will receive open kinetic chain exercises only, including stretching and strengthening exercises for knee flexors and extensors. They will be expected to maintain their current level of physical activity and go about their daily lives as usual.
Adherence:
The percentage of total intervention days completed will be used to determine adherence. 12 sessions = 100%.
Sample size estimation: A G-power grogram for windows is used to calculate the estimated sample size with an effect size of 0.25 and an alpha error probability of 0.90 to detect the changes in three groups receiving three independent interventions for four dependent variables. The measurement will be repeated twice across the study period. The statistical test used is the Multivariate Analysis of variance (MANOVA), and the total sample size will be 36. The number will be increased for possible dropout to 45 patients with 15 patients in each group. Statistical Analysis The study's findings will be presented in accordance with CONSORT.
Statistical analysis: will be carried out with the help of statistical software such as SPSS. Patients' demographic data will be presented as mean and standard deviation. Analysis of the patients' age (years), weight (Kg), height (cm), and body mass index (BMI) kg/m2 will be performed by one-way analysis of variance (ANOVA) to detect the similarity in subjects between the treatment groups. Three treatment groups that received three different interventions will be measured twice at pre-treatment and post-treatment. To detect changes in the dependent variables within and between groups, one-way repeated measures Multivariate analysis (MANOVA) will be applied. If there is a significant change within groups or between tests, the post hoc Bonferroni test will be used to detect the significance between each group and/or each level of measurement. The level of significance is p\<0.05. The data will be analyzed with the intention to treat principles. Each paper from the project will be subjected to a statistical analysis publication plan.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SEQUENTIAL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Graded weight-bearing exercise
participants will perform exercises using an anti-gravity treadmill
anti-gravity treadmill
participants will perform exercises with partial weight-bearing by using an anti-gravity treadmill
Closed kinetic chain exercise
Exercises will be achieved in a weight-bearing position, with or without support, besides other exercises to improve knee flexors and extensors strength.
Weight-bearing exercises for knee flexors and extensors
Stretching and strengthening exercises will be performed in a weight-bearing position
open kinetic chain exercise
Exercises including stretching and strengthening exercises for knee flexors and extensors
Non weight-bearing exercises for knee flexors and extensors
Stretching and strengthening exercises will be performed in a non-weight-bearing position
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
anti-gravity treadmill
participants will perform exercises with partial weight-bearing by using an anti-gravity treadmill
Weight-bearing exercises for knee flexors and extensors
Stretching and strengthening exercises will be performed in a weight-bearing position
Non weight-bearing exercises for knee flexors and extensors
Stretching and strengthening exercises will be performed in a non-weight-bearing position
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The x-ray showed grades II and III according to on Kallgren and Lawrence (K/L) grading system.
* Patients are willing to stop medications.
* Patients accepted to assign informed consent to participate in the current study and will attend the lab twice a week for six successive weeks.
Exclusion Criteria
* Previous knee surgery/injection for the last six months.
* Previous knee fracture or malignancy.
* Unable to walk unaided.
* Unable to commit study requirements.
40 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Umm Al-Qura University
OTHER
Imam Abdulrahman Bin Faisal University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ammar Fadil
Principle Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ammar S Fadil, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Imam Abdulrahman Bin Faisal University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Umm Al-Qura University
Mecca, Western Chapter, Saudi Arabia
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
IRB-PGS-2022-03-447
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.