- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05470790
Arabic Version of Marx Activity Rating and Knee Stability in Sports/Cutting-Pivoting Ability Scales
May 11, 2025 updated by: Majed Ali AlAbbad, Imam Abdulrahman Bin Faisal University
Cross-Cultural Adaptation and Psychometric Properties Analysis of Arabic Version of Marx Activity Rating Scale and Knee Stability in Sports/Cutting-Pivoting Ability Scale for Saudi Athletes With Anterior Cruciate Ligament Injury
Anterior cruciate ligament (ACL) injuries are among the most common knee ligament injuries, causing joint instability and impairments.
Besides being challenging, this type of injury greatly affects the athlete's passion and wellbeing, and it is associated with several risk factors.
Injuries to the ACL are estimated to occur within 80,000 to 250,000 young, active and healthy athletes each year.
This cross-sectional observational study aimed at translating, adapting cross-culturally, and investigating the psychometric properties of the Marx Activity Rating Scale (MARS) and the Knee Stability in Sports/Cutting-Pivoting Ability (KSS/CPA) scale in Saudi patients with anterior cruciate ligament injuries.
For this study, a convenient sample size of 100 athletes with ACL injuries and healthy participants will be selected from different Saudi hospitals and clubs.
Study participants will be informed about the study and a consent form will be obtained before they participate.
A number of scales will be used as outcome measures, including the MARS, KSS/CPA scale, Knee Injury, and Osteoarthritis Outcome Score, Lysholm Knee Score, and International Knee Documentation Committee Subjective Knee Form.
Internal consistency of both the MARS and KSS/CPA scales will be tested using Cronbach's alpha.
A construct's validity will be measured by Spearman's correlation coefficient.
Content validity can be determined by examining whether there are floor and ceiling effects.
A significance level of 0.05 will be used to determine whether the data is significant.
Ultimately, the study will help patients with ACL injuries to make informed decisions about their treatment, empower healthcare professionals to understand patients' concerns, and facilitate research.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Majed Ali Alabbad, MSc
- Phone Number: 966569877985
- Email: majed2031@gmail.com
Study Locations
-
-
Eastern Province
-
Dammam, Eastern Province, Saudi Arabia, 2435
- Recruiting
- Imam Abdulrahman Bin Faisal University
-
Contact:
- Fuad Abdulla, PhD
- Email: faabdullah@iau.edu.sa
-
-
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
18 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
sports population
Description
Inclusion Criteria:
- An athlete with an orthopedic diagnosis of unilateral ACL injury
- Age from 18 years to 45 years old
- Participants who read and write in Arabic
- Healthy participants that do not have lower limb injury limited participation in physical activity for at least six months.
Exclusion Criteria:
- 1 Patients with other lower limbs or different musculoskeletal injuries such as lower back pain may affect physical activity
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
control
|
Activity Rating Scale, Knee Stability in Sports/Cutting-Pivoting Ability scale, Knee Injury and Osteoarthritis Outcome Score, Lysholm Knee Score, and International Knee Documentation Committee Subjective Knee Form.
|
|
athletes with anterior cruciate ligament injuries
|
Activity Rating Scale, Knee Stability in Sports/Cutting-Pivoting Ability scale, Knee Injury and Osteoarthritis Outcome Score, Lysholm Knee Score, and International Knee Documentation Committee Subjective Knee Form.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Arabic version of Marx activity rating scale
Time Frame: 1 minute
|
The arabic version of Marx activity rating scale measures four activities: running, deceleration, cutting, and pivoting; higher scores indicate an increased frequency of knee-related activities.
The frequency of performing these activities in the past 12 months is measured on a five-point scale.
Based on the four items, the maximum score is 16 (if they answer "four or more times a week" for all four), and the minimum score is zero.
For each item, one point will be awarded for each frequency category, beginning with "one time every month."
and if participants answered "less than once a month" for one of the items, they will be awarded zero points; "once in a month," one point; "once a week," two points; etc.
|
1 minute
|
|
Arabic version of knee stability in sports/cutting -pivoting ability scale
Time Frame: 1 minute
|
The items in the Arabic version of knee stability in sports/cutting -pivoting ability scale are ranked on a Likert scale of 1 to 5, with response categories consisting of (A) normal, (B) near-normal, (C) abnormal, (D) severe abnormal, and (E) dysfunctional.
knee stability in sports is a scale that emphasizes giving way to sensations and instability in the knees during linear activities (i.e., running in straight lines, accelerating, and decelerating), which involve lower-level motions.
The cutting -pivoting ability scale section concerns the frequency, ability, and discomfort of performing pivotal activities.
However, the ordinal knee stability in sports/cutting -pivoting ability scale will be converted into continuous variables (A = 100, B = 75, C = 50, D = 25, E = 0) and an overall self-assessment evaluation of knee function (0 = worst, 100 = best) will be recorded.
|
1 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Injury and Osteoarthritis Outcome Score
Time Frame: 3 minutes
|
There are five subscales with 42 items in the Knee Injury and Osteoarthritis Outcome Score questionnaire: Pain (9 items), Symptoms (7 items), Activities of Daily Living (17 items), Sport and Recreation (5 items), and Knee-related Quality of Life (QoL4).
Each item wil be scored using a Likert scale ranging from 0 (no problem) to 4 (extreme problem).
In addition, the subscale items will be rated on a scale of 0 to 100 using the following formula (100*average of subscale item scores/4*100), and higher scores indicate better health (100 = no knee problems) while low scores indicate poor health.
|
3 minutes
|
|
Lysholm Knee Score
Time Frame: 2 minutes
|
Eight categories will be measured in the Lysholm Knee Score: instability (25 marks), pain (25 marks), catching (15 marks), stair climbing (10 marks), swelling (10 marks), need for support (5 marks), squatting (5 marks), and limping (5 marks).
Each answer to the eight questions counts toward the total score, ranging from 0 to 100.
High scores indicate better results and fewer symptoms.
Lower scores indicate a problem with knee function.
|
2 minutes
|
|
International Knee Documentation Committee Subjective Knee Form
Time Frame: 2 minutes
|
There are three main sections in the International Knee Documentation Committee Subjective Knee Form, overall consisting of 18 items: (1) symptoms (7 items), including swelling, pain, stiffness, giving way, and locking, (2) sports (1 item), (3) current knee function (9 items), and knee function after a knee injury (1 item) (not included in the overall score).
The International Knee Documentation Committee Subjective Knee Form will be calculated by adding the scores of the individual items.
The score will be then transformed into an overall score ranging from 0 to 100, with 100 indicating the absence of symptoms and higher levels of functioning.
A total score of 100 will be calculated as (sum of items)/ (maximum possible score).
|
2 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
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)
May 1, 2022
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
July 20, 2022
First Submitted That Met QC Criteria
July 20, 2022
First Posted (Actual)
July 22, 2022
Study Record Updates
Last Update Posted (Actual)
May 14, 2025
Last Update Submitted That Met QC Criteria
May 11, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- QCH-SREC0 4 /2022
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
IPD will not be shared
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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