Patellofemoral Pain SyndromeNCT06347406
Effects of Combined Physiotherapy Management and Education
A study testing Blood flow restriction combined with physiotherapy and education in people with Patellofemoral Pain Syndrome, run by Fakulti Sains Kesihatan at 1 site in Malaysia.
Trial summary
This observational study aims to determine the effects of combined physiotherapy programs and education in patellofemoral pain syndrome. The main questions it aims to answer are: Are there any effects of combined physiotherapy program among individuals with PFPS on: i) Pain ii) Muscle functions (strength, muscle bulk… Read more about this study
- Who is it for?
- Ages 18 to 59 yearsHealthy volunteers can take part
- Conditions the study is for
- Patellofemoral Pain Syndrome
- What is being tested?
- Blood flow restriction combined with physiotherapy and education
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 128 participants
- Where
- 1 siteMalaysia
- Study dates
- 1 Apr 2024to 1 Apr 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 18 to 59 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Pain and disability in at least three of the following activities involving pain around the patella
- Scored in KOOS-PF
Who cannot join
- Failure to regularly continue treatment sessions
- A history of knee surgery and severe trauma with meniscus or ligament tear within 6 months
- Went for acupuncture treatment
- Undergone any type of surgical procedure
- Pregnancy, cancer, secondary osteoarthritis and various rheumatologic diseases, and symptoms of abnormal neurological examination of sensation, movement, and reflexes
Trial locations and contacts
1 site in 1 country.
Malaysia1 site, 1 recruiting
- Recruiting
Fakulti Sains Kesihatan
Shah Alam, Selangor, 42300
Zarina Zahari, 0132094170, zarinazahari@uitm.edu.my
Nurul Atiqah Mohamed Mosbi, 603-3258 4300, atiqahmosbi@uitm.edu.my
About this study
Official title: Effects of Combined Physiotherapy Management and Education on Physiological Functions and Quality of Life Among Individuals With Patellofemoral Pain
This observational study aims to determine the effects of combined physiotherapy programs and education in patellofemoral pain syndrome. The main questions it aims to answer are:
- Are there any effects of combined physiotherapy program among individuals with PFPS on:
Read more
- Pain ii) Muscle functions (strength, muscle bulk, flexibility) iii) Knee muscle functional performance (anteromedial lunge, step-down, bilateral squat, and balance and reach) iv) Kinesiophobia v) Quality of life Participants will be
- Measure for the anthropometrics data including body weight, height, and BMI.
- Answer the Numerical Pain Rating scale
- Abswe Malay version of KOOS-PF and TAMPA scale.
- Once they finished with the questionnaire, the participants will be stationed into station 1 (HDD), station 2 (Realtime Ultrasound) and station 3 (Dartfish Motion Analysis) Treatment they will receive
- Blood flow restrictions cuff with physiotherapy exercises
- Patient education Researcher will compare Blood flow exercises combined with physiotherapy exercises and education (Group A) with Physiotherapy exercises (Group B) to see if there is an effect on i) Pain ii) Muscle Functions (strength, muscle bulk, flexibility iii) Functional performance (anteromedial lunge, step-down, bilateral squat, balance, and reach) iv) Kinesiophobia v) Quality of life
Read the detailed description
The participants who volunteered will be screened for inclusion and exclusion criteria. Prior to the assessments and examinations, the physiotherapist in charge will explain the study and will get consent from the participants. This study will follow the Consort RCT 2010 guidelines.
Then the participants will go into randomization sequence before they go into the interventions. The participants will go into block randomization. The participants will be blocks into color (Blue for Experimental group, Red for control group). This study will be double blinded. The blinded person will be the accessors and the participants.
Then they will complete the demographic questionnaire which will include questions on personal data, health status, medical illness, past medical history, simple questions on their pain, site of pain with the assistance by the researchers to read the questions as most of the participants is illiterate.
Then the participants will be measure for the anthropometric data including body weight, height and BMI.
The participants will answer the Numerical Pain Rating scale, KOOS-PF Malay version and TAMPA scale. Then they will proceed with station 1 (HHD which measure strength), station 2 (Real time ultrasound which measure muscle bulk) and then station 3 (Dartfish motion analysis for knee functional performance test (anteromedial lunge, step-down, single-leg press, bilateral squat, and balance and reach) using the Dartfish software.
Station 1 (HDD) will be conducted by a physiotherapist who specially trained to do the HDD. The physiotherapist will then measure the Quadriceps and Hamstrings. These were the procedures that the physiotherapist needs to do:
- Quadriceps Procedure: Allow for free hanging of the leg at a 90-degree angle. Place the HDD just proximal to the lateral and medial maleolis. Instruct the individual to reach full knee extension effort in 1-2 seconds and then sustain it for an additional 2-3 seconds. Ascertain that the subject's leg is fully stretched away from their body.
- Hamstrings Procedure: In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force.In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force. In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force.
After the participant completed with the station 1, then he/she will be proceeded with Station 2 (Real time ultrasound).
Procedure: To prevent hip external rotation when supine, a strap was attached around both participant's feet. A 38 mm, 13e18Hz linear transducer was placed above each pen-marked spot to get ultrasonic readings (HDI3000 by Advanced Technology Laboratories, California). The photographs were taken by a technician or a physiotherapist (which one is available) who had received training in real-time ultrasonography. Gain was increased until muscle borders appeared on the screen, and the picture depth was adjusted until the femur was visible in the screen's central. Each muscle, namely the vastus medialis (VM), the vastus lateralis (VL), the vastus intermedius (VI), the rectus femoris (RF), and the vastus medialis (VM), semimembranousus (SM), semitendinosus (ST) and Biceps Femoris (BF). Iliotibial band (ITB), tenssofacialate (TFL) and gastrocnemius (GSN) will be photographed three times. To minimize muscular stiffness, the transducer head was adequately covered in ultrasonic gel.
Once completed with the station 2, then the participant will proceed with station 3 (Knee Muscle performance Test with Dartfish motion software). This station will be conducted by a physiotherapist who trained in Dartfish motion analysis software.
Procedure:
The participant is dressed in compression shorts and shirt that fit tightly to the body. The lower extremity model that utilizes four markers placed in various locations from the acromion joint, greater trochanteric, medial tuberosity of femur down to the lateral malleolus. After the marker is install on the participant body, they are requiring to perform these movements:
Anteromedial lunge left and right: The subject is positioned behind a starting line. The subject lunges forward with the uninvolved limb so that the front leg bends to 90 degrees and crosses the midline. The patient must keep his or her balance and maintain an upright trunk posture. The participant is then instructed to perform as many lunges in 30 seconds; lunges that do not meet the 80% level are not recorded. The lunge is not included in the count if the subject deviates from the path of motion or takes an extra step.
Step-down, left and right: The step-down is a unilateral test done from an 8-inch (20.32-centimeter) high platform. Participant take a step forward and lower themselves to the ground. Only the heel of the down leg brushes the floor before returning to full knee extension. This is considered one repeat. This to allow to calculate the time take to complete one cycle and speed (Refer to Appendix E). The trunk, hip, knee and ankle ROM is calculate when the both foot touches the step and when the test foot starting to go down to the ground. Both limbs are put to the test
Bilateral squat: The participant begin by standing with their legs fully extended, shoulders shoulder-width apart, and their weight evenly distributed on both limbs. Participant lower their bodies to a 90 degrees knee position before returning to full extension. A complete cycle of straight standing to 90 degrees of knee flexion and back to straight standing constitutes one repeat (speed and time of this cycle will be calculate.
Balance and reach (to measure distance) : Behind a start line, the subject begins the test. The participant extends one leg straight forward until the heel contacts the floor, with the rear (test) leg bearing most of the body weight. The unaffected limb is put to the test first. Measurement between the starting point to end point will be calculated
Once they completed the questionnaire and assessment, then the participant will proceed with the interventions.
The participant will need to strap proximal parts of the lower limb with 40% of subject's RECOVER FUN AIR CUFF WITH PUMP. The timer will be set up to 10 minutes during the intervention for the participants' to release the pressure of the cuff. The participants' will rest on the chair for 5 minutes. The participants will need to perform physiotherapy exercises with the cuff on.
Education booklet will be designed to educate the participants about the PFPS, advice and importance of exercises.
The contain of this booklet consist of:
- What is PFPS
- What causes PFPS
- What are the symptoms of PFPS?
- Pain gate theory
- Importance of treatment
- Exercises
- Frequently asked questions
Follow up Participants will need to come in for intervention for three times a week for 12 weeks.
- Conditions
- Patellofemoral Pain Syndrome
- Being tested
- Blood flow restriction combined with physiotherapy and education
- Medical subject headings
- Patellofemoral Pain Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Blood flow restriction combined with physiotherapy and educationOther
Also called Linda Physiotherapy programme
Blood flow restriction Physiotherapy exercises Education
| Study group | Role | What they receive |
|---|---|---|
| Blood flow restriction combined with physiotherapy and education | Experimental | Blood flow restriction, combined with physiotherapy exercises and patient education Receives: Other: Blood flow restriction combined with physiotherapy and education |
| Control Group | Placebo comparator | physiotherapy exercises Receives: Other: Blood flow restriction combined with physiotherapy and education |
What is being measured
The primary outcome is the main question the study is designed to answer.
Numerical Pain Rating
On a Numerical Pain Rating Scale, often known as an NPRS, patients are asked to circle the number between 0 and 10, 0 and 20, or 0 and 100 that most properly portrays the intensity of pain that they are experiencing
Measured: 4 months
The Knee injury and Osteoarthritis Outcome Score for patellofemoral pain and osteoarthritis (KOOS-PF)
The KOOS-PF subscale is used to assess pain and function in the patellofemoral joint. The 11-point KOOS-PF, which was created in collaboration with healthcare professionals, demonstrated adequate measuring qualities and is recommended for clinical and research usage in patients suffering from patellofemoral pain
Measured: 4 months
Tampa Scale
The Tampa Kinesiophobia Scale (TSK) is a self-assessment measure used to determine a person's fear of movement-related pain who suffers from musculoskeletal discomfort
Measured: 4 months
Hand held dynamometer (HDD)
The examiner holds a small portable gadget against the patient's limb during a maximal isometric contraction. The equipment can test both the proximal and distal muscles of all extremitie
Measured: 4 months
Knee Muscle performance Test with Dartfish software
Dartfish data will be used to process the action of anteromedial lunge, step-down, bilateral squat, and balance and reach during simultaneous digital video acquisition. In other words, Dartfish programme will generate data. All of these movements will be measured with Dartfish software
Measured: 4 months
Real time ultrasounds
The thickness and length of the superficial quadriceps muscles (VMO, VL, VL, and RF).
Measured: 4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2024
- Study start1 Apr 2024 (estimated)
- Primary completion1 Apr 2025 (estimated)
- Study completion1 Apr 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patellofemoral Pain SyndromeStudies 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
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 128 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fakulti Sains Kesihatan
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06347406
- Sponsor's protocol ID
- FSKesihatan
- Status last verified
- Mar 2024
- First submitted
- 29 Mar 2024
- Last updated
- 4 Apr 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Combined Physiotherapy Management and Education on Physiological Functions and Quality of Life Among Individuals With Patellofemoral Pain
- ClinicalTrials.gov ID
- NCT06347406
- Acronym / sponsor ID
- FSKesihatan
- Conditions
- Patellofemoral Pain Syndrome
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 128 participants (estimated)
- Lead sponsor
- Fakulti Sains KesihatanUniversity, hospital or other
- Study start
- 1 Apr 2024 (estimated)
- Primary completion
- 1 Apr 2025 (estimated)
- Study completion
- 1 Apr 2025 (estimated)
- First posted
- 4 Apr 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 observational study aims to determine the effects of combined physiotherapy programs and education in patellofemoral pain syndrome. The main questions it aims to answer are:
- Are there any effects of combined physiotherapy program among individuals with PFPS on:
- Pain ii) Muscle functions (strength, muscle bulk, flexibility) iii) Knee muscle functional performance (anteromedial lunge, step-down, bilateral squat, and balance and reach) iv) Kinesiophobia v) Quality of life Participants will be
- Measure for the anthropometrics data including body weight, height, and BMI.
- Answer the Numerical Pain Rating scale
- Abswe Malay version of KOOS-PF and TAMPA scale.
- Once they finished with the questionnaire, the participants will be stationed into station 1 (HDD), station 2 (Realtime Ultrasound) and station 3 (Dartfish Motion Analysis) Treatment they will receive
- Blood flow restrictions cuff with physiotherapy exercises
- Patient education Researcher will compare Blood flow exercises combined with physiotherapy exercises and education (Group A) with Physiotherapy exercises (Group B) to see if there is an effect on i) Pain ii) Muscle Functions (strength, muscle bulk, flexibility iii) Functional performance (anteromedial lunge, step-down, bilateral squat, balance, and reach) iv) Kinesiophobia v) Quality of life
Detailed description
The participants who volunteered will be screened for inclusion and exclusion criteria. Prior to the assessments and examinations, the physiotherapist in charge will explain the study and will get consent from the participants. This study will follow the Consort RCT 2010 guidelines.
Then the participants will go into randomization sequence before they go into the interventions. The participants will go into block randomization. The participants will be blocks into color (Blue for Experimental group, Red for control group). This study will be double blinded. The blinded person will be the accessors and the participants.
Then they will complete the demographic questionnaire which will include questions on personal data, health status, medical illness, past medical history, simple questions on their pain, site of pain with the assistance by the researchers to read the questions as most of the participants is illiterate.
Then the participants will be measure for the anthropometric data including body weight, height and BMI.
The participants will answer the Numerical Pain Rating scale, KOOS-PF Malay version and TAMPA scale. Then they will proceed with station 1 (HHD which measure strength), station 2 (Real time ultrasound which measure muscle bulk) and then station 3 (Dartfish motion analysis for knee functional performance test (anteromedial lunge, step-down, single-leg press, bilateral squat, and balance and reach) using the Dartfish software.
Station 1 (HDD) will be conducted by a physiotherapist who specially trained to do the HDD. The physiotherapist will then measure the Quadriceps and Hamstrings. These were the procedures that the physiotherapist needs to do:
- Quadriceps Procedure: Allow for free hanging of the leg at a 90-degree angle. Place the HDD just proximal to the lateral and medial maleolis. Instruct the individual to reach full knee extension effort in 1-2 seconds and then sustain it for an additional 2-3 seconds. Ascertain that the subject's leg is fully stretched away from their body.
- Hamstrings Procedure: In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force.In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force. In a prone position, the knee was flexed to 15° and 90° of flexion, as determined by ocular judgement. The examiner positioned the HHD at the subject's heel and gradually increased the force applied to the calcaneal for 1-2 seconds. The individual will be instructed to resist the applied force.
After the participant completed with the station 1, then he/she will be proceeded with Station 2 (Real time ultrasound).
Procedure: To prevent hip external rotation when supine, a strap was attached around both participant's feet. A 38 mm, 13e18Hz linear transducer was placed above each pen-marked spot to get ultrasonic readings (HDI3000 by Advanced Technology Laboratories, California). The photographs were taken by a technician or a physiotherapist (which one is available) who had received training in real-time ultrasonography. Gain was increased until muscle borders appeared on the screen, and the picture depth was adjusted until the femur was visible in the screen's central. Each muscle, namely the vastus medialis (VM), the vastus lateralis (VL), the vastus intermedius (VI), the rectus femoris (RF), and the vastus medialis (VM), semimembranousus (SM), semitendinosus (ST) and Biceps Femoris (BF). Iliotibial band (ITB), tenssofacialate (TFL) and gastrocnemius (GSN) will be photographed three times. To minimize muscular stiffness, the transducer head was adequately covered in ultrasonic gel.
Once completed with the station 2, then the participant will proceed with station 3 (Knee Muscle performance Test with Dartfish motion software). This station will be conducted by a physiotherapist who trained in Dartfish motion analysis software.
Procedure:
The participant is dressed in compression shorts and shirt that fit tightly to the body. The lower extremity model that utilizes four markers placed in various locations from the acromion joint, greater trochanteric, medial tuberosity of femur down to the lateral malleolus. After the marker is install on the participant body, they are requiring to perform these movements:
Anteromedial lunge left and right: The subject is positioned behind a starting line. The subject lunges forward with the uninvolved limb so that the front leg bends to 90 degrees and crosses the midline. The patient must keep his or her balance and maintain an upright trunk posture. The participant is then instructed to perform as many lunges in 30 seconds; lunges that do not meet the 80% level are not recorded. The lunge is not included in the count if the subject deviates from the path of motion or takes an extra step.
Step-down, left and right: The step-down is a unilateral test done from an 8-inch (20.32-centimeter) high platform. Participant take a step forward and lower themselves to the ground. Only the heel of the down leg brushes the floor before returning to full knee extension. This is considered one repeat. This to allow to calculate the time take to complete one cycle and speed (Refer to Appendix E). The trunk, hip, knee and ankle ROM is calculate when the both foot touches the step and when the test foot starting to go down to the ground. Both limbs are put to the test
Bilateral squat: The participant begin by standing with their legs fully extended, shoulders shoulder-width apart, and their weight evenly distributed on both limbs. Participant lower their bodies to a 90 degrees knee position before returning to full extension. A complete cycle of straight standing to 90 degrees of knee flexion and back to straight standing constitutes one repeat (speed and time of this cycle will be calculate.
Balance and reach (to measure distance) : Behind a start line, the subject begins the test. The participant extends one leg straight forward until the heel contacts the floor, with the rear (test) leg bearing most of the body weight. The unaffected limb is put to the test first. Measurement between the starting point to end point will be calculated
Once they completed the questionnaire and assessment, then the participant will proceed with the interventions.
The participant will need to strap proximal parts of the lower limb with 40% of subject's RECOVER FUN AIR CUFF WITH PUMP. The timer will be set up to 10 minutes during the intervention for the participants' to release the pressure of the cuff. The participants' will rest on the chair for 5 minutes. The participants will need to perform physiotherapy exercises with the cuff on.
Education booklet will be designed to educate the participants about the PFPS, advice and importance of exercises.
The contain of this booklet consist of:
- What is PFPS
- What causes PFPS
- What are the symptoms of PFPS?
- Pain gate theory
- Importance of treatment
- Exercises
- Frequently asked questions
Follow up Participants will need to come in for intervention for three times a week for 12 weeks.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Blood flow restriction combined with physiotherapy and education | Experimental | Other: Blood flow restriction combined with physiotherapy and educationBlood flow restriction, combined with physiotherapy exercises and patient education |
| Control Group | Placebo comparator | Other: Blood flow restriction combined with physiotherapy and educationphysiotherapy exercises |
Who may qualify
- Ages
- 18 to 59 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Pain and disability in at least three of the following activities involving pain around the patella
- Scored in KOOS-PF
Key exclusion criteria (5 listed)
- Failure to regularly continue treatment sessions
- A history of knee surgery and severe trauma with meniscus or ligament tear within 6 months
- Went for acupuncture treatment
- Undergone any type of surgical procedure
- Pregnancy, cancer, secondary osteoarthritis and various rheumatologic diseases, and symptoms of abnormal neurological examination of sensation, movement, and reflexes
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 |
|---|---|---|
| Blood flow restriction combined with physiotherapy and educationAlso: Linda Physiotherapy programmeBlood flow restriction Physiotherapy exercises Education | Other | Blood flow restriction combined with physiotherapy and education, Control Group |
Primary outcome
Numerical Pain Rating
Time frame: 4 months
On a Numerical Pain Rating Scale, often known as an NPRS, patients are asked to circle the number between 0 and 10, 0 and 20, or 0 and 100 that most properly portrays the intensity of pain that they are experiencing
The Knee injury and Osteoarthritis Outcome Score for patellofemoral pain and osteoarthritis (KOOS-PF)
Time frame: 4 months
The KOOS-PF subscale is used to assess pain and function in the patellofemoral joint. The 11-point KOOS-PF, which was created in collaboration with healthcare professionals, demonstrated adequate measuring qualities and is recommended for clinical and research usage in patients suffering from patellofemoral pain
Tampa Scale
Time frame: 4 months
The Tampa Kinesiophobia Scale (TSK) is a self-assessment measure used to determine a person's fear of movement-related pain who suffers from musculoskeletal discomfort
Hand held dynamometer (HDD)
Time frame: 4 months
The examiner holds a small portable gadget against the patient's limb during a maximal isometric contraction. The equipment can test both the proximal and distal muscles of all extremitie
Knee Muscle performance Test with Dartfish software
Time frame: 4 months
Dartfish data will be used to process the action of anteromedial lunge, step-down, bilateral squat, and balance and reach during simultaneous digital video acquisition. In other words, Dartfish programme will generate data. All of these movements will be measured with Dartfish software
Real time ultrasounds
Time frame: 4 months
The thickness and length of the superficial quadriceps muscles (VMO, VL, VL, and RF).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Apr 2024.
- Individual participant dataSharing planned: No
Related trials for Patellofemoral Pain Syndrome
Recruiting
Effects of Telerehabilitation Versus Supervised Rehabilitation Protocol on Pain, Range of Motion and Functional Recovery in Patients With Patellofemoral Pain Syndrome.
Patello Femoral Pain Syndrome
RecruitingObservational study
MRI Study of Musculoskeletal Function
Abnormalities, Imaging
Not yet recruiting
Comparison of High-Intensity and Conventional Physical Therapy in Musculoskeletal Disorders
Low Back Pain, Radicular Syndrome
Active, not recruiting
Stabilization vs Corrective Exercise in PFP
Patellofemoral Pain Syndrome
Not yet recruiting
Effectiveness of Selected Traditional Chinese Medicine Topical Agents on Long Distance Runner Versus Exercise Therapy as Control for Patellofemoral Pain Syndrome
Patellar Femoral Syndrome, TCMO (Ng's Prescription)
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. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Blood flow restriction combined with physiotherapy and education in people with Patellofemoral Pain Syndrome, run by Fakulti Sains Kesihatan at 1 site in Malaysia.
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 2 inclusion and 5 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: status not confirmed, as of the sponsor's last update on 4 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Malaysia. 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. Some participants in this study may receive a placebo. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Aslinda Maulat Mohd Fuhad (0169818007, lindalance87@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Numerical Pain Rating (time frame: 4 months). The study lists 6 primary outcomes in all. 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 4 Apr 2024.