Meniscus TearNCT06532851
The Effect of Therapeutic Exercise on Cartilage Morphology and Physical Function for Individuals at High Risk of Knee Osteoarthritis
A study testing Progressive Resistance Exercise (PRE) and Aerobic Exercise in people with Meniscus Tear, run by Jordan University of Science and Technology at 2 sites in Jordan.
Trial summary
This randomized controlled trial aims to evaluate the efficacy of progressive resistance exercises (PRE) versus aerobic exercises on cartilage morphology and physical function in patients with degenerative meniscus tears. Read more about this study
- Who is it for?
- Ages 35 to 55 yearsHealthy volunteers can take part
- Conditions the study is for
- Meniscus Tear
- What is being tested?
- Progressive Resistance Exercise (PRE) and Aerobic Exercise
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 2 sitesJordan
- Study dates
- 1 Jun 2023to 1 Mar 2031
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 35 to 55 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Are between 35 and 55 years of age.
- Have a symptomatic degenerative medial meniscus tear as evidenced by:
- Presence of medial knee pain.
- Medial joint line tenderness.
- Pain and limited motion when attempting to perform a full squat and
- Increased intra-meniscal signal on at least 2 consecutive MRI slices and
- Have clearance from their personal physician to participate in an exercise program.
Who cannot join
- Radiographic evidence of OA (K-L grade 2 or above).
- A repairable meniscus injury (longitudinal tear in the outer 1/3 of the meniscus).
- A meniscus injury that requires meniscectomy (locked knee).
- Prior or current ligament injury or surgery of the involved knee.
- Prior or current injury or surgery to contra-lateral knee.
- Pathological ligamentous laxity upon examination of the knee
Show all 14Show fewer
- An inflammatory arthritic condition or
- Any injury or condition involving the lower extremities that affects their ability to walk.
- Because participation in this study requires undergoing MRI, subjects will be excluded if they:
- If female, pregnant at the time of enrollment.
- Had prior surgery for an aneurysm; any medical illness that may interfere with the patient's general fitness or exercise capability.
- Had any contraindication with MRI.
- Had surgery within the past two months.
- Have a cardiac pacemaker.
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Jordan2 sites, 2 recruiting
- Recruiting
King Abdullah University Hospital
Ar Ramtha
Khaldoon Bashaireh, MD, 0096227200600, bashaireh@just.edu.jo
- Recruiting
Jordan University of Science and Technology
Irbid
Mohammad Yabroudi, PhD, 0096227201000 ext. 26936, m.yabroudi@just.edu.jo
About this study
Official title: The Efficacy of Progressive Resistance Exercises Versus Aerobic Exercises on Cartilage Morphology and Physical Function in Patients With Degenerative Meniscus Tear: A Randomized Controlled Trial
This randomized controlled trial aims to evaluate the efficacy of progressive resistance exercises (PRE) versus aerobic exercises on cartilage morphology and physical function in patients with degenerative meniscus tears. 45 participants, aged 35-55, will be randomly assigned to one of three groups: PRE, aerobic exercise, or control (standard of care physical and medical therapy). The study will utilize MRI T2 mapping to assess changes in cartilage composition and patient-reported and performance-based measures to evaluate clinical outcomes. This pilot study will also determine the feasibility and issues related to recruitment and retention for a larger trial.
Read the detailed description
Background: Degenerative meniscus tears are common in individuals over 35 and are associated with early stages of knee osteoarthritis (OA) (1,2). Metabolic and microstructural changes within the cartilage occur before surface breakdown, which can now be detected using advanced MRI techniques such as T2 mapping. Exercise therapy, specifically progressive resistance and aerobic exercises, has shown benefits for knee OA patients, but its effects on early cartilage degeneration are poorly understood.
Objective: The primary objective of this study is to determine the efficacy of PRE and aerobic exercises on the metabolic function and microstructure of cartilage in individuals with degenerative meniscus tears but without radiographic evidence of knee OA. Secondary objectives include evaluating the impact of these exercises on clinical outcomes, such as pain, disability, and physical function, and assessing the feasibility of recruitment and retention for a larger trial.
Methods: The study will enroll 54 participants, who will be randomized into three groups: PRE, aerobic exercise, and control. Each group will undergo a 3-month supervised exercise program. MRI scans will be used to measure changes in cartilage composition, while clinical outcomes will be assessed using patient-reported and performance-based measures.
Intervention Groups:
Group 1 (PRE): Participants will perform progressive resistance exercises focusing on strengthening the quadriceps. The exercises will be adjusted based on the Daily Adjustable Progressive Resistance Exercise (DAPRE) technique.
Group 2 (Aerobic Exercise): Participants will engage in aerobic exercise sessions using a stationary bike, aimed at improving cardiovascular fitness and knee joint mobility.
Group 3 (Control): Participants will receive standard of care, including general strength and balance exercises as per current clinical guidelines.
Assessments:
MRI Imaging: Advanced MRI techniques (T2 mapping) will be used at baseline and after 3 months to assess changes in cartilage composition.
Clinical Outcomes: Patient-reported outcomes will include the Knee Injury and Osteoarthritis Outcome Score (KOOS) and the International Knee Documentation Committee (IKDC) score. Performance-based outcomes will include the single-leg squat, single-leg hop test, sit-to-stand on a one-foot test, step-up test, and Bruce treadmill test.
Inclusion Criteria:
Adults aged 35-55 years Symptomatic degenerative medial meniscus tears. No radiographic evidence of knee OA (Kellgren-Lawrence grade 0-1). Ability to provide informed consent. Willingness to participate in the exercise intervention.
Exclusion Criteria:
Existing diagnosis of knee OA (Kellgren-Lawrence grade 2 or higher). Repairable meniscus injuries or prior meniscus repair. Previous knee surgery or significant knee injury within the past 6 months. Presence of inflammatory arthritis or other significant comorbidities. Contraindications to MRI or inability to participate in exercise programs.
Study Outcomes:
Primary Outcomes: Changes in T2 relaxation times in the cartilage, indicating alterations in cartilage composition and health.
Secondary Outcomes: Improvements in clinical outcomes, including pain, disability, and physical function as measured by KOOS, IKDC, and performance-based tests.
Feasibility Metrics: Recruitment rates, adherence to the exercise program, and retention rates over the study period.
Analysis: A mixed ANOVA will be used to compare changes in outcomes between groups, with adjustments for multiple comparisons. Baseline characteristics will be compared using t-tests and chi-square tests.
- Conditions
- Meniscus Tear
- Being tested
- Progressive Resistance Exercise (PRE), Aerobic Exercise, Control
- Keywords
- Degenerative Meniscus Tear, MRI T2 Mapping, Progressive Resistance Exercise, Aerobic Exercise, Knee Pain, Cartilage Morphology, Exercise Therapy, Early Knee Osteoarthritis
- Medical subject headings
- Osteoarthritis, Knee
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Progressive Resistance Exercise (PRE)Other
Also called Exercise Therapy, Resistance Training
A structured exercise regimen focusing on increasing muscular strength and endurance through progressive resistance.
Aerobic ExerciseOther
Also called Exercise Therapy, Aerobic Training
An exercise program focusing on cardiovascular conditioning using a stationary bike.
ControlOther
Also called Comparator
A set of general strength and balance exercises that do not target the specific therapeutic goals of the other interventions.
| Study group | Role | What they receive |
|---|---|---|
| Progressive Resistance Exercise (PRE) | Experimental | Participants will perform progressive resistance exercises focusing on strengthening the quadriceps muscles. The exercises will be adjusted based on the Daily Adjustable Progressive Resistance Exercise (DAPRE) technique. Receives: Other: Progressive Resistance Exercise (PRE) |
| Aerobic Exercise | Experimental | Participants will engage in aerobic exercise sessions using a stationary bike, aimed at improving cardiovascular fitness and knee joint mobility. Receives: Other: Aerobic Exercise |
| Control | Active comparator | Participants will receive standard of care, including general strength and balance exercises as per current clinical guidelines. Receives: Other: Control |
What is being measured
The primary outcome is the main question the study is designed to answer.
Short echo T2*
Short echo time T2* imaging is used to diagnose early cartilage degeneration. T2* measures the rate at which the MRI signal decays, particularly focusing on short-T2 signals (less than 10 milliseconds) which decay rapidly (3-6).
Measured: Baseline, 3-month, 24-month, and 5 years follow-ups.
Secondary outcomes (8)
Single leg hop test for a distance
The Single Leg Hop Test for distance is one of four assessments used to evaluate athletes' horizontal movement capabilities. These tests, collectively known as the 4 Single Leg Hop Tests, were established by Noyes et al (7). They include the Triple Hop for distance, the Single Leg Hop Test for distance, the 6-meter hop for time, and the Crossover Hop for distance.
In the Single Leg Hop Test for distance, participants stand on one leg with their toes aligned along a designated landmark line. They then execute a forward hop, landing eccentrically while maintaining balance on the tested leg. The examiner measures the distance from the initial landmark line to the point where the participant's heel contacts the ground (8).
This test is valuable for assessing lower extremity strength, power, and balance. It has been shown to be a reliable and valid measure for evaluating aspects of lower extremity function (9-10).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Single Leg Squat Test
The Single Leg Squat Test is a functional movement assessment used to evaluate lower extremity strength, neuromuscular control, and stability. Beyond its focus on lower limb function, it also helps identify core muscle strength and provides insights into an individual's capabilities in cutting, running, and landing (11). The SLST assesses the ability to alternate between concentric and eccentric contractions of the knee and hip muscles (12).
In the test, the patient stands on one leg with their foot aligned with a straight line. The examiner assists with balance and ensures proper form. The patient then performs knee bends until the line along their toes is no longer visible, within a 30-degree range of knee flexion. Each patient has 30 seconds to complete as many repetitions as possible, with the maximum number recorded (13-16). The physiotherapist monitors and adjusts the test to maintain accuracy and consistency.
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Timed Stair Climbing Test (SCT)
The Timed Stair Climbing Test (SCT) is a functional performance assessment designed to evaluate lower extremity strength, endurance, and functional mobility. Participants will ascend and descend a 12-step staircase, with each step measuring 18 cm in height and 28 cm in depth. The objective is to complete the test as quickly as possible while ensuring a sense of safety and comfort. While the use of one handrail is optional, participants are encouraged to refrain from using it (17).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Single Leg Chair Rise (SLCR) test
The Single Leg Chair Rise (SLCR) test evaluates quadriceps strength and can also help diagnose mid-lumbar nerve root impingement and radiculopathy (18,19). It has a sensitivity of 0.48, a specificity of 0.90, a positive likelihood ratio of 4.60, and a negative likelihood ratio of 0.58 (19).
The protocol uses a 45.7 cm chair. Participants, dressed and shod, sit with arms crossed, the tested leg flexed at 90 degrees, and the other leg extended without touching the ground. They rise to full knee extension and then return to the seated position to complete one repetition. The test includes two assessments: one measuring endurance with as many repetitions as possible in 30 seconds, and another measuring power by completing five repetitions as quickly as possible. Each test is performed twice, with the best score recorded (20).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Maximal voluntary isometric contraction test
To assess quadriceps muscle strength, the maximum voluntary isometric torque test will be performed using an isokinetic dynamometer (Biodex System 3 Pro). The procedure involves the participant seated with their ankle positioned in line with the dynamometer's axis at 60 degrees of knee flexion, secured by waist, thigh, and chest straps (21).
Before testing, participants will familiarize themselves with the process by performing isometric contractions at 50%, 75%, and 100% of their maximal effort. During the actual test, they will exert maximal force against the dynamometer's fixed arm for knee extension. Each participant will complete three trials with a two-minute rest between them, aiming to match or exceed a target torque displayed on a screen. The target torque will be adjusted based on their performance in previous trials. The maximum quadriceps muscle strength will be calculated using the recorded data (21).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Modified Bruce Treadmill Testing Protocol
The modified Bruce Test is designed for sedentary and elderly patients to estimate maximal oxygen consumption (VO2max) and assess aerobic endurance. Unlike the standard Bruce Test, which includes seven stages of increasing speed and incline on a treadmill, the modified version starts with a lower workload. It begins at 1.7 km/hr with a 0% incline and progresses to a 5% incline in the second stage, before resembling the first stage of the standard test. This modified approach includes "Stage Zero" and "1/2" to indicate the initial zero incline and a slight incline in the following stage, making it more suitable for less fit individuals (22,23).
VO2max measures the maximum amount of oxygen a person uses during intense exercise. It is calculated based on the duration of exercise using different formulas for men and women, without needing to measure inhaled and exhaled air directly (22,23):
Women: VO2max (ml/kg/min) = 4.38 × T - 3.9 Men: VO2max (ml/kg/min) = 2.94 × T + 7.65
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
International Knee Documentation Committee Subjective Knee Form (IKDC)
The International Knee Documentation Committee Subjective Knee Form (IKDC) was developed in 2001 through a collaboration between the European Society for Sports Traumatology, Knee Surgery, and Arthroscopy, and the American Orthopaedic Society for Sports Medicine (AOSSM). This form is a widely used patient-reported outcome measure that assesses subjective aspects of a patient's health related to knee conditions. It includes domains such as symptoms, functional limitations, and sports activities. The IKDC has been translated into numerous languages, including Arabic for this study. It comprises ten questions, with one evaluating the impact of the knee on daily activities and nine focusing on performance. Scores range from 0 to 100, with higher scores indicating better health status (24).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Knee injury and Osteoarthritis Outcomes Score (KOOS)
The Knee Injury and Osteoarthritis Outcomes Score (KOOS) is a patient-reported outcome measure designed to assess the impact of knee injury or osteoarthritis on an individual's quality of life (25,26). It includes subscales for pain, symptoms, activities of daily living (ADL), quality of life, and recreational activities (25,26). Studies have shown that KOOS has superior psychometric characteristics compared to other measures. It has been translated into 40 languages, including an Arabic version for use in Saudi Arabia, which will be utilized in our study (27,28). KOOS comprises 42 items across five subscales: nine for pain, seven for symptoms, seventeen for ADL, five for sports and recreation function, and four for knee-related quality of life. Each item is scored from 0 to 4, with higher scores indicating better health status (29).
Measured: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2024
- Study start1 Jun 2023
- Primary completion1 Dec 2030 (estimated)
- Study completion1 Mar 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Meniscus TearStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- In this model, participants are assigned to one of the three groups (PRE, aerobic exercise, control) and remain in that group for the duration of the study. Each group receives a different intervention, allowing for direct comparisons between the interventions.
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Jordan University of Science and Technology
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06532851
- Sponsor's protocol ID
- 20230630
- Status last verified
- May 2026
- First submitted
- 29 Jul 2024
- Last updated
- 12 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Efficacy of Progressive Resistance Exercises Versus Aerobic Exercises on Cartilage Morphology and Physical Function in Patients With Degenerative Meniscus Tear: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT06532851
- Acronym / sponsor ID
- 20230630
- Conditions
- Meniscus Tear
- Keywords
- Degenerative Meniscus Tear, MRI T2 Mapping, Progressive Resistance Exercise, Aerobic Exercise, Knee Pain, Cartilage Morphology, Exercise Therapy, Early Knee Osteoarthritis
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Jordan University of Science and TechnologyUniversity, hospital or other
- Study start
- 1 Jun 2023 (actual)
- Primary completion
- 1 Dec 2030 (estimated)
- Study completion
- 1 Mar 2031 (estimated)
- First posted
- 1 Aug 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This randomized controlled trial aims to evaluate the efficacy of progressive resistance exercises (PRE) versus aerobic exercises on cartilage morphology and physical function in patients with degenerative meniscus tears. 45 participants, aged 35-55, will be randomly assigned to one of three groups: PRE, aerobic exercise, or control (standard of care physical and medical therapy). The study will utilize MRI T2 mapping to assess changes in cartilage composition and patient-reported and performance-based measures to evaluate clinical outcomes. This pilot study will also determine the feasibility and issues related to recruitment and retention for a larger trial.
Detailed description
Background: Degenerative meniscus tears are common in individuals over 35 and are associated with early stages of knee osteoarthritis (OA) (1,2). Metabolic and microstructural changes within the cartilage occur before surface breakdown, which can now be detected using advanced MRI techniques such as T2 mapping. Exercise therapy, specifically progressive resistance and aerobic exercises, has shown benefits for knee OA patients, but its effects on early cartilage degeneration are poorly understood.
Objective: The primary objective of this study is to determine the efficacy of PRE and aerobic exercises on the metabolic function and microstructure of cartilage in individuals with degenerative meniscus tears but without radiographic evidence of knee OA. Secondary objectives include evaluating the impact of these exercises on clinical outcomes, such as pain, disability, and physical function, and assessing the feasibility of recruitment and retention for a larger trial.
Methods: The study will enroll 54 participants, who will be randomized into three groups: PRE, aerobic exercise, and control. Each group will undergo a 3-month supervised exercise program. MRI scans will be used to measure changes in cartilage composition, while clinical outcomes will be assessed using patient-reported and performance-based measures.
Intervention Groups:
Group 1 (PRE): Participants will perform progressive resistance exercises focusing on strengthening the quadriceps. The exercises will be adjusted based on the Daily Adjustable Progressive Resistance Exercise (DAPRE) technique.
Group 2 (Aerobic Exercise): Participants will engage in aerobic exercise sessions using a stationary bike, aimed at improving cardiovascular fitness and knee joint mobility.
Group 3 (Control): Participants will receive standard of care, including general strength and balance exercises as per current clinical guidelines.
Assessments:
MRI Imaging: Advanced MRI techniques (T2 mapping) will be used at baseline and after 3 months to assess changes in cartilage composition.
Clinical Outcomes: Patient-reported outcomes will include the Knee Injury and Osteoarthritis Outcome Score (KOOS) and the International Knee Documentation Committee (IKDC) score. Performance-based outcomes will include the single-leg squat, single-leg hop test, sit-to-stand on a one-foot test, step-up test, and Bruce treadmill test.
Inclusion Criteria:
Adults aged 35-55 years Symptomatic degenerative medial meniscus tears. No radiographic evidence of knee OA (Kellgren-Lawrence grade 0-1). Ability to provide informed consent. Willingness to participate in the exercise intervention.
Exclusion Criteria:
Existing diagnosis of knee OA (Kellgren-Lawrence grade 2 or higher). Repairable meniscus injuries or prior meniscus repair. Previous knee surgery or significant knee injury within the past 6 months. Presence of inflammatory arthritis or other significant comorbidities. Contraindications to MRI or inability to participate in exercise programs.
Study Outcomes:
Primary Outcomes: Changes in T2 relaxation times in the cartilage, indicating alterations in cartilage composition and health.
Secondary Outcomes: Improvements in clinical outcomes, including pain, disability, and physical function as measured by KOOS, IKDC, and performance-based tests.
Feasibility Metrics: Recruitment rates, adherence to the exercise program, and retention rates over the study period.
Analysis: A mixed ANOVA will be used to compare changes in outcomes between groups, with adjustments for multiple comparisons. Baseline characteristics will be compared using t-tests and chi-square tests.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 3
- Model description
- In this model, participants are assigned to one of the three groups (PRE, aerobic exercise, control) and remain in that group for the duration of the study. Each group receives a different intervention, allowing for direct comparisons between the interventions.
| Arm | Type | Receives |
|---|---|---|
| Progressive Resistance Exercise (PRE) | Experimental | Other: Progressive Resistance Exercise (PRE)Participants will perform progressive resistance exercises focusing on strengthening the quadriceps muscles. The exercises will be adjusted based on the Daily Adjustable Progressive Resistance Exercise (DAPRE) technique. |
| Aerobic Exercise | Experimental | Other: Aerobic ExerciseParticipants will engage in aerobic exercise sessions using a stationary bike, aimed at improving cardiovascular fitness and knee joint mobility. |
| Control | Active comparator | Other: ControlParticipants will receive standard of care, including general strength and balance exercises as per current clinical guidelines. |
Who may qualify
- Ages
- 35 to 55 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (7 listed)
- Are between 35 and 55 years of age.
- Have a symptomatic degenerative medial meniscus tear as evidenced by:
- Have clearance from their personal physician to participate in an exercise program.
Key exclusion criteria (14 listed)
- Radiographic evidence of OA (K-L grade 2 or above).
- A repairable meniscus injury (longitudinal tear in the outer 1/3 of the meniscus).
- A meniscus injury that requires meniscectomy (locked knee).
- Prior or current ligament injury or surgery of the involved knee.
- Prior or current injury or surgery to contra-lateral knee.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Progressive Resistance Exercise (PRE)Also: Exercise Therapy, Resistance TrainingA structured exercise regimen focusing on increasing muscular strength and endurance through progressive resistance. | Other | Progressive Resistance Exercise (PRE) |
| Aerobic ExerciseAlso: Exercise Therapy, Aerobic TrainingAn exercise program focusing on cardiovascular conditioning using a stationary bike. | Other | Aerobic Exercise |
| ControlAlso: ComparatorA set of general strength and balance exercises that do not target the specific therapeutic goals of the other interventions. | Other | Control |
Primary outcome
Short echo T2*
Time frame: Baseline, 3-month, 24-month, and 5 years follow-ups.
Short echo time T2* imaging is used to diagnose early cartilage degeneration. T2* measures the rate at which the MRI signal decays, particularly focusing on short-T2 signals (less than 10 milliseconds) which decay rapidly (3-6).
8 secondary outcomes
Single leg hop test for a distance
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Single Leg Squat Test
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Timed Stair Climbing Test (SCT)
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Single Leg Chair Rise (SLCR) test
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Maximal voluntary isometric contraction test
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Modified Bruce Treadmill Testing Protocol
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
International Knee Documentation Committee Subjective Knee Form (IKDC)
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
The Knee injury and Osteoarthritis Outcomes Score (KOOS)
Time frame: Baseline, 6-week, immediately post-intervention, 6-month, 9-month, and 5 years follow-ups.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2026.
- (1) Englund M, Roos EM, Roos HP, Lohmander LS. Patient-relevant outcomes fourteen years after meniscectomy: influence of type of meniscal tear and size of resection. Rheumatology. 2001 Jun;40(6):631-9.Link provided by the sponsor.
- (2) Wolf BR, Gulbrandsen TR. Degenerative Meniscus Tear in Older Athletes. Clin Sports Med. 2020 Jan;39(1):197-209.Link provided by the sponsor.
- (3) Carlier PG, Bertoldi D, Baligand C, Wary C, Fromes Y. Muscle blood flow and oxygenation measured by NMR imaging and spectroscopy. NMR Biomed. 2006 Nov;19(7):954-67.Link provided by the sponsor.
- (4) Gatehouse PD, Bydder GM. Magnetic Resonance Imaging of Short T2 Components in Tissue. Clin Radiol. 2003 Jan;58(1):1-19.Link provided by the sponsor.
- (5) Gatehouse PD, Thomas RW, Robson MD, Hamilton G, Herlihy AH, Bydder GM. Magnetic resonance imaging of the knee with ultrashort TE pulse sequences. Magn Reson Imaging. 2004 Oct;22(8):1061-7.Link provided by the sponsor.
- (6) Qian Y, Boada FE. Acquisition-weighted stack of spirals for fast high-resolution three-dimensional ultra-short echo time MR imaging. Magn Reson Med. 2008 Jul;60(1):135-45.Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Jordan University of Science and Technology
Irbid, Jordan
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Progressive Resistance Exercise (PRE) and Aerobic Exercise in people with Meniscus Tear, run by Jordan University of Science and Technology at 2 sites in Jordan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 12 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Jordan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Short echo T2* (time frame: Baseline, 3-month, 24-month, and 5 years follow-ups.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2026.