AzTrials
AzTrials

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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

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

Other trials in Pakistan

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.

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 groups in NCT05863806
Study groupRoleWhat they receive
Mulligan MobilzationExperimentalMWM 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 MassageActive comparatorTransverse 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.

  1. 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)
  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.

  1. First posted18 May 2023
  2. Study start1 Oct 2022
  3. Primary completion20 Jun 2023
  4. Study completion30 Jun 2023

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in