Rotator Cuff SyndromeNCT05863806
Mulligan Mobilization vs Transverse Friction Massage in Rotator Cuff Syndrome
A study testing Mulligan Mobilzation and Trasverse Friction Massage in people with Rotator Cuff Syndrome, run by Riphah International University at 1 site in Pakistan.
Trial summary
The aim of this research is to determine the Effects of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome. Randomized clinical trials will be done at Northwest General Hospital, Peshawar. The sample size is 42. Read more about this study
- Who is it for?
- Ages 30 to 70 years
- Conditions the study is for
- Rotator Cuff Syndrome
- What is being tested?
- Mulligan Mobilzation and Trasverse Friction Massage
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 42 participants
- Where
- 1 sitePakistan
- Study dates
- 1 Oct 2022to 30 Jun 2023
- 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 30 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Both Male and Female are included
- Age between 30 to 70
- Partial rupture and suffering from rotator cuff syndrome(differentiation is made on type of tear from grade 0 to 3)
- No shoulder surgery
- Pain on palpation of rotator cuff muscle
- Two or more provocative tests should be positive which is used to rule out the tendonitis and bursitis.
Who cannot join
- Multiple shoulder pathologies.
- Bursitis
- Corticosteroid injections last month
- Orthopedic or cardiovascular problem
- Recent myocardial infarction or major shoulder trauma
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Northwest General Hospital and Research Center
Peshawar, Khyber Pakhtunkhwa, 25000
About this study
Official title: Comparison of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome
The aim of this research is to determine the Effects of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome. Randomized clinical trials will be done at Northwest General Hospital, Peshawar. The sample size is 42. The subjects were divided in two groups, with 21 subjects in Group A and 21 in Group B. Study duration was of 6 months. Sampling technique applied was Non probability Purposive Sampling technique. Both males and females of aged 30-70 years with rotator cuff syndrome from grade (0-3) were included. Tools used in the study are Visual Analogue Scale (VAS), Goniometer, and DASH (Disabilities of the Arm, Shoulder and Hand) questionnaire. Data was analyzed through SPSS 23.
Read the detailed description
The rotator cuff syndrome is developed in the subacromial area by compression between the humerus and the coracoacromial arc of the long head of the subacromial bursa and the biceps tendon. The diagnosis of rotator cuff tendonitis and Bursitis is made on the basis of special tests and Examination. The rotator cuff tendons undergo degenerative alterations, the tendons between the humeral head and the coracoacromial arch are compressed and ischemia caused by impingement or elevated intramuscular pressure is all aspects of the physiopathology of RCS.
Highly exposed workers have frequently had RCS associated with biomechanical, psychological, and organizational aspects examined; this could affect generalizations to the entire working population who are exposed to varying degrees of work-related shoulder restrictions. The relationship between work structure and the risk of shoulder illnesses has been rarely investigated. Although various individual factors can raise the incidence of shoulder discomfort and RCS, biomechanical factors are significantly linked to both conditions (e.g., age).
Neer defined the syndrome as impingement of the rotator cuff tendons against the coracoacromial ligament, the anterior edge and undersurface of the anterior part of the acromion, and, often, the acromioclavicular joint. There is consensus that risk factors for shoulder MSDs are upper arm elevation and repeated or prolonged overhead activities in combination with other biomechanical variables (e.g., repetition, force). There is less proof that excessive repetition or rigid shoulder positions are separate risk factors.
The main focus in Rotator Cuff syndrome management is on promoting self-management, reducing pain, optimize function, and modifying the disease process and its effects. The primary treatment for Rotator Cuff syndrome conservatively is physiotherapy which includes strength training, modalities, resistance training and Kinesiotaping. Resistance exercise can reduce Shoulder pain severity and strength in participants with symptomatic Shoulder RCS. Exercise is suggested as the first-line intervention of choice with comparable outcomes but at a lower cost and with fewer associated hazards than surgical therapy in recent randomized controlled studies and systematic reviews. Despite this, there is little evidence that explains what an effective exercise programmed looks like in terms of the kind of exercise, the number of sets and repetitions, tolerable pain levels, duration, and environment.
Mulligan's mobilization with movement (MWM) is a joint mobilization treatment in which the patient actively engages in the uncomfortable action while receiving a manual accessory glide to one of the joint surfaces. Recent research found that in asymptomatic people applying MWM with a postero-lateral glide resulted in less muscular activity in the shoulder muscles . In accordance with Cyriax, Transverse friction massage leads in traumatic hyperemia, which boosts blood flow and lessens discomfort. It also stimulates mechanoreceptors and enhances tissue perfusion.
- Conditions
- Rotator Cuff Syndrome
- Being tested
- Mulligan Mobilzation, Trasverse Friction Massage
- Keywords
- Mulligan mobilization, Transverse Friction Massage, Rotator cuff syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mulligan MobilzationOther
Participants were instructed that MWM, including shoulder movement, must be pain-free and should be immediately stopped if any pain is experienced during the treatment.
The single session of MWM technique was last around 20 minutes, in 3 sets of 10 repetitions with a rest interval of 30 seconds between each sets.
Trasverse Friction MassageOther
Deep friction massage was given to rotator cuff tendon with the tip of index finger, which is reinforced by middle finger.
It was given in transverse direction for 10 - 12 minutes. Transverse friction massage was Given twice a week with the gap of days for the first 3 week and then the repetition is increased to 3 to 4 times a week for the rest of duration.
| Study group | Role | What they receive |
|---|---|---|
| Mulligan Mobilzation | Experimental | MWM technique was carrying out in flexion, abduction, external and internal rotation directions. For this technique, participants were seated on a stretcher, and the physical therapist is standing opposite of the upper extremity that is treated. The internal hand of the physical therapist stabilizes participants' shoulder girdle and, with the thenar eminence of the other hand, performed a glide of the humeral head (this direction is the most suitable for treating such shoulder limitations).
Participants were asked to flex the affected shoulder until the pain started while the physical therapist sustained the gliding force to the humeral head. The single session of MWM technique was last around 20 minutes, in 3 sets of 10 repetitions with a rest interval of 30 seconds between each sets. Receives: Other: Mulligan Mobilzation |
| Trasverse Friction Massage | Active comparator | Transverse Friction Massage technique: Patients in the group B were receiving soft tissue massage (deep friction) is made to bend his/ her elbow to 90o and put forearm behind his/ her back, then lean back in half lying position. Thus arm is fixed in adduction and medial rotation. It was given in transverse direction for 10 - 12 minutes. Transverse friction massage was given twice a week with the gap of days for the first 3 week and then the repetition is increased to 3 to 4 times a week for the rest of duration. Receives: Other: Trasverse Friction Massage |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change from baseline in Disability of Arm, Shoulder and Hand Questionnaire
Change from baseline the DASH score at 3rd and 6th week. The DASH (Disabilities of the Arm, Shoulder and Hand) Outcome Measure is a 30-item, self-report questionnaire that measures physical function and symptoms in people with musculoskeletal disorders of the upper limb. Changes from the baseline, and then at 3rd and 6th week
Measured: 6th week
Secondary outcomes (1)
Change from baseline in Visual Analogue Scale
Change from baseline the Visual Analogue Scale score at 3rd and 6th week. A device used by physical therapists to measure joints' range of motion. During measurement fulcrum will be placed on shoulder joint parallel to sagittal axis for abduction and adduction, frontal axis for flexion and extension and to humeral longitudinal axis in 90o of abduction for internal and external rotations. Changes from the baseline, and then at 3rd and 6th week
Measured: 6th week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 May 2023
- Study start1 Oct 2022
- Primary completion20 Jun 2023
- Study completion30 Jun 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rotator Cuff SyndromeStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- 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
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 42 participants (actual)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Muhammad Affan Iqbal, PhD*, Principal investigator, Riphah International UniversityAsad Khan, MSPT*, Principal investigator, Northwest General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05863806
- Sponsor's protocol ID
- REC/01494
- Status last verified
- Jul 2023
- First submitted
- 4 May 2023
- Last updated
- 27 Jul 2023
- Results posted
- No
- Data monitoring committee
- 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 27 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome
- ClinicalTrials.gov ID
- NCT05863806
- Acronym / sponsor ID
- REC/01494
- Conditions
- Rotator Cuff Syndrome
- Keywords
- Mulligan mobilization, Transverse Friction Massage, Rotator cuff syndrome
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 42 participants (actual)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 1 Oct 2022 (actual)
- Primary completion
- 20 Jun 2023 (actual)
- Study completion
- 30 Jun 2023 (actual)
- First posted
- 18 May 2023 (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.
The aim of this research is to determine the Effects of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome. Randomized clinical trials will be done at Northwest General Hospital, Peshawar. The sample size is 42. The subjects were divided in two groups, with 21 subjects in Group A and 21 in Group B. Study duration was of 6 months. Sampling technique applied was Non probability Purposive Sampling technique. Both males and females of aged 30-70 years with rotator cuff syndrome from grade (0-3) were included. Tools used in the study are Visual Analogue Scale (VAS), Goniometer, and DASH (Disabilities of the Arm, Shoulder and Hand) questionnaire. Data was analyzed through SPSS 23.
Detailed description
The rotator cuff syndrome is developed in the subacromial area by compression between the humerus and the coracoacromial arc of the long head of the subacromial bursa and the biceps tendon. The diagnosis of rotator cuff tendonitis and Bursitis is made on the basis of special tests and Examination. The rotator cuff tendons undergo degenerative alterations, the tendons between the humeral head and the coracoacromial arch are compressed and ischemia caused by impingement or elevated intramuscular pressure is all aspects of the physiopathology of RCS.
Highly exposed workers have frequently had RCS associated with biomechanical, psychological, and organizational aspects examined; this could affect generalizations to the entire working population who are exposed to varying degrees of work-related shoulder restrictions. The relationship between work structure and the risk of shoulder illnesses has been rarely investigated. Although various individual factors can raise the incidence of shoulder discomfort and RCS, biomechanical factors are significantly linked to both conditions (e.g., age).
Neer defined the syndrome as impingement of the rotator cuff tendons against the coracoacromial ligament, the anterior edge and undersurface of the anterior part of the acromion, and, often, the acromioclavicular joint. There is consensus that risk factors for shoulder MSDs are upper arm elevation and repeated or prolonged overhead activities in combination with other biomechanical variables (e.g., repetition, force). There is less proof that excessive repetition or rigid shoulder positions are separate risk factors.
The main focus in Rotator Cuff syndrome management is on promoting self-management, reducing pain, optimize function, and modifying the disease process and its effects. The primary treatment for Rotator Cuff syndrome conservatively is physiotherapy which includes strength training, modalities, resistance training and Kinesiotaping. Resistance exercise can reduce Shoulder pain severity and strength in participants with symptomatic Shoulder RCS. Exercise is suggested as the first-line intervention of choice with comparable outcomes but at a lower cost and with fewer associated hazards than surgical therapy in recent randomized controlled studies and systematic reviews. Despite this, there is little evidence that explains what an effective exercise programmed looks like in terms of the kind of exercise, the number of sets and repetitions, tolerable pain levels, duration, and environment.
Mulligan's mobilization with movement (MWM) is a joint mobilization treatment in which the patient actively engages in the uncomfortable action while receiving a manual accessory glide to one of the joint surfaces. Recent research found that in asymptomatic people applying MWM with a postero-lateral glide resulted in less muscular activity in the shoulder muscles . In accordance with Cyriax, Transverse friction massage leads in traumatic hyperemia, which boosts blood flow and lessens discomfort. It also stimulates mechanoreceptors and enhances tissue perfusion.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Mulligan Mobilzation | Experimental | Other: Mulligan MobilzationMWM technique was carrying out in flexion, abduction, external and internal rotation directions. For this technique, participants were seated on a stretcher, and the physical therapist is standing opposite of the upper extremity that is treated. The internal hand of the physical therapist stabilizes participants' shoulder girdle and, with the thenar eminence of the other hand, performed a glide of the humeral head (this direction is the most suitable for treating such shoulder limitations). Participants were asked to flex the affected shoulder until the pain started while the physical therapist sustained the gliding force to the humeral head. The single session of MWM technique was last around 20 minutes, in 3 sets of 10 repetitions with a rest interval of 30 seconds between each sets. |
| Trasverse Friction Massage | Active comparator | Other: Trasverse Friction MassageTransverse Friction Massage technique: Patients in the group B were receiving soft tissue massage (deep friction) is made to bend his/ her elbow to 90o and put forearm behind his/ her back, then lean back in half lying position. Thus arm is fixed in adduction and medial rotation. It was given in transverse direction for 10 - 12 minutes. Transverse friction massage was given twice a week with the gap of days for the first 3 week and then the repetition is increased to 3 to 4 times a week for the rest of duration. |
Who may qualify
- Ages
- 30 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Both Male and Female are included
- Age between 30 to 70
- Partial rupture and suffering from rotator cuff syndrome(differentiation is made on type of tear from grade 0 to 3)
- No shoulder surgery
- Pain on palpation of rotator cuff muscle
Key exclusion criteria (5 listed)
- Multiple shoulder pathologies.
- Bursitis
- Corticosteroid injections last month
- Orthopedic or cardiovascular problem
- Recent myocardial infarction or major shoulder trauma
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 |
|---|---|---|
| Mulligan MobilzationParticipants were instructed that MWM, including shoulder movement, must be pain-free and should be immediately stopped if any pain is experienced during the treatment. The single session of MWM technique was last around 20 minutes, in 3 sets of 10 repetitions with a rest interval of 30 seconds between each sets. | Other | Mulligan Mobilzation |
| Trasverse Friction MassageDeep friction massage was given to rotator cuff tendon with the tip of index finger, which is reinforced by middle finger. It was given in transverse direction for 10 - 12 minutes. Transverse friction massage was Given twice a week with the gap of days for the first 3 week and then the repetition is increased to 3 to 4 times a week for the rest of duration. | Other | Trasverse Friction Massage |
Primary outcome
Change from baseline in Disability of Arm, Shoulder and Hand Questionnaire
Time frame: 6th week
Change from baseline the DASH score at 3rd and 6th week. The DASH (Disabilities of the Arm, Shoulder and Hand) Outcome Measure is a 30-item, self-report questionnaire that measures physical function and symptoms in people with musculoskeletal disorders of the upper limb. Changes from the baseline, and then at 3rd and 6th week
1 secondary outcome
Change from baseline in Visual Analogue Scale
Time frame: 6th week
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Jul 2023.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
Muhammad Affan Iqbal, PhD* principal investigator
Riphah International University
Asad Khan, MSPT* principal investigator
Northwest General Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Mulligan Mobilzation and Trasverse Friction Massage in people with Rotator Cuff Syndrome, run by Riphah International University at 1 site in Pakistan.
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 6 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: finished, as of the sponsor's last update on 27 Jul 2023. 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 Pakistan. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change from baseline in Disability of Arm, Shoulder and Hand Questionnaire (time frame: 6th week). 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 27 Jul 2023.