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Trapezius Muscle StrainNCT05125484

Comparison of Bowen's Technique and Myofascial Release Technique On Pain And Disability in Trapezitis

A study testing experimental Bowen Technique and Experimental Myofacial release technique in people with Trapezius Muscle Strain, 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
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Trial summary

The aim of this research is to compare the effects of Bowen's technique and Myofascial Release technique on pain and disability in patients with trapezitis.Randomized controlled trials done at Islamabad Physiotherapy and Rehabilitation Centre(IPRC) and Benazir Bhutto Hospital. The sample size was 66. Read more about this study

Who is it for?
Ages 20 to 40 years
Conditions the study is for
Trapezius Muscle Strain
What is being tested?
experimental Bowen Technique and Experimental Myofacial release technique
Could I receive a placebo?
No, everyone receives an active treatment
How many people
66 participants
Where
1 sitePakistan
Study dates
16 Nov 2021to 1 Feb 2022
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 20 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Both male and female.
  • Age 20-40 years.
  • Clinically diagnosed with Trapezitis.(Spasm,stiffness,Tenderness,Trigger Points,Taut band)
  • Cummulative trauma disorder
  • Occupational overuse syndrome

Who cannot join

  • Any medical conditions or diseases that could interfere with intervention performance.
  • Any traumatic neck injury
  • Cervical vertebral fracture
  • Cervical spinal cord compromise/ cervical myelopathy
  • Cervical radiculopathy
  • Cervical Spondylolisthesis
  • Any tumour
  • Any degenerative diseases

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Benazir Bhutto Hospital

    Rawalpindi, Punjab Province, 46000

Other trials in Pakistan

About this study

Official title: Comparison Of Bowen's Technique And Myofascial Release Technique On Pain And Disability In Patients With Trapezitis

The aim of this research is to compare the effects of Bowen's technique and Myofascial Release technique on pain and disability in patients with trapezitis.Randomized controlled trials done at Islamabad Physiotherapy and Rehabilitation Centre(IPRC) and Benazir Bhutto Hospital. The sample size was 66. The subjects were divided in two groups, 33 subjects in Bowen's Technique group and 33 subjects in Myofascial Release Technique group. Study duration was of 6 months. Sampling technique applied was non probability purposive sampling technique. The patients aged 20-40 years and clinicaly diagnosed with Trapezitis(spasm,trigger points,tenderness,stiffness) were included in the study. Tools used in the study are Cervical ROMs, NPRS, NDI, Isometric Scapular Pinch Test and Lateral Scapular Slide Test.

Read the detailed description

Trapezitis is a condition that involves inflammation of the trapezius muscle. The upper fibers of trapezius, being the postural muscles, are highly susceptible to overuse injuries and thus the inflammation.This results in pain that is present during the rest, is aggravated with activity and is referred to the other areas. The pain results in protective spasm of the antagonistic muscle group that also restricts the passive range of motion and makes it painful too. In people working for long hours at a desk and computers or spending many hours driving, the low level of upper trapezius activity is frequently found because of head posture during sitting and standing , which is common cause of tension and neck pain in such people.Various recent studies have hypothesized that trapezitis occurs due to muscle tissue overloading and injury, that results in involuntary shortening of localized muscle fibers. The stressed soft tissue area thus receives less glucose, oxygen and nutrients supply; subsequently high levels of metabolic waste products are accumulated. And this cascade of events ends in altered status of tissue, pain and the development of the Trigger points in the muscle.

Myofascial Release(MFR) is a soft tissue mobilization technique that is defined as " the facilitation of mechanical, neural and psycho physiological adaptive potential as interfaced via the myofascial system".MFR decreases the pain and restores the proper alignment by changing the ground substance's viscosity to more fluid state resulting in elimination of excessive pressure of fascia on the pain sensitive structures.

There is one more soft tissue technique called 'Bowen Technique' that is useful and indicated in myofascial pain. The Bowen technique is defined as:

'…dynamic system of muscle and connective tissue therapy which balances the body to allow it to heal itself. The work consists of a series of precise moves on specific points of the body. These moves are light and can be done through clothing. There are frequent and important pauses between each series of moves giving the body time to benefit from each. The technique uses positive moves that initiate a positive energy flow and negative moves that isolate this energy to a specific area' (Rentsch and Rentsch,1997) The Bowen technique was developed by late Tom Bowen in Geelong, Australia in 1950. It is a connective tissue technique that uses subtle inputs called 'Bowen moves' to the body that stimulates the body's self-healing. The Bowen moves applied are in several sets in a complete session of 15-45 minutes duration. While applying the technique, the therapist uses the thumb when the Bowen move is executed away from the patient's body and two fingers are used when the Bowen move is executed towards the patient's body. The technique can be used anywhere on the origin, insertion or the belly of the muscle and produces a physical and an energetic action.

This technique can be used to treat many types acute and chronic injuries and other health issues. It does this by using holistic approach in which body's innate healing mechanism is stimulated. This technique has been recommended in many conditions like headache, cervical pain, back pain, whiplash injury, TMJ dysfunction, herniated disk, tennis elbow, hamstring tightness and frozen shoulder, work related injuries etc.

An RCT was done by Ekta S. Chaudhary, Nehal Shah, Neeta Vyas, Ratan Khuman1, Dhara Chavda1, Gopal Nambi that compared the effectiveness of MFR and cold pack in Upper trapezius Spasm and concluded both MFR and cold pack along with exercises to be effective in upper trapezium muscle spasm but the overall effects of MFR surpassed the cold therapy. Another study by Pooja Mane , Amrutkuvar Pawar , Trupti Warude compared the effects of Myofascial Release technique with Deep Friction Massage on pain and cervical ROM, the results concluded both therapies to bring improvement in pain and cervical ROM but MFR was more effective. Similarly, a systematic review of RCTs was conducted to determine the effectiveness of MFR in decreasing pain , improving function and elongate length and concluded MFR to be emerging strategy with strong evidence base and solid treatment option for many conditions. A study was conducted to compare the effects of MFR with hot pack in reducing pain and improving passive ROM in shoulder joint and that concluded both to be effective but MFR proved to be more favorable because of the less time spent and no need of equipment.

A study has been done to see the effects of Bowen technique as an adjunct therapy to conventional physiotherapy treatment on the pain and functional outcomes in patient with Acute trapezitis and the results established Bowen technique to be effective in decreasing pain and improving functional outcomes in Acute trapezitis.A few studies were conducted that evaluated the effectiveness of Bowen technique in frozen shoulder and concluded this technique as a positive intervention in improving mobility, functional status and decreasing pain. A few studies were conducted that compared the effects of Bowen technique vs MET in treatment of hamstring tightness.And few other worked to establish the effectiveness of Bowen technique in different complex and common conditions and found positive results.A study was done to show Bowen technique to be effective in health service workplace to improve physical as well as mental well-being of the working staff.

This study aims to compare the short term effects of Bowen Technique and MFR on pain and neck disability in patients with trapezitis. Also it intends to study the short term effects of both techniques on scapular motions. Bowen technique is a relatively new technique, having easier application and has been less worked on. So, if this study proves the effectiveness of Bowen technique in comparison with MFR in patient with trapezitis. Further studies can be conducted to evaluate its efficacy as an independent and preferable procedure in treatment of other conditions and further work can be conducted on other areas as well. As this is a holistic technique, so it could be a beneficial addition in the daily clinical practice.

Being tested
experimental Bowen Technique, Experimental Myofacial release technique
Keywords
Bowen therapy, Myofacial Release Technique, Isometric Scapular pinch test, Lateral Scapular Slide test, NDI

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • experimental Bowen TechniqueOther

    Patient was in lying position. Therapist placed thumb on the effected side muscke. Then hooked thumb on lateral edge of muscle to apply pressure against the muscle. Took a pause. Thumb flattened in a medial direction and pluck was created in muscle.

    Set of 15-20 bowen moves on upper , middle and lower fibres each with 2 mins gap between each set.

    Total treatment time: 20 mins

  • Experimental Myofacial release techniqueOther

    Patient was in lying position. MFR applied via ulnar border of both palms while patient being in contralateral side flexion.

    20 mins

Study groups in NCT05125484
Study groupRoleWhat they receive
Experimental Intervention group 1ExperimentalPatient was in lying position. Therapist placed thumb on the effected side muscke. Then hooked thumb on lateral edge of muscle to apply pressure against the muscle. Took a pause. Thumb flattened in a medial direction and pluck was created in muscle. Set of 15-20 bowen moves on upper , middle and lower fibres each with 2 mins gap between each set. Total treatment time: 20 mins
Receives: Other: experimental Bowen Technique
Experimental interventional group IIExperimentalPatient was in lying position. MFR applied via ulnar border of both palms while patient being in contralateral side flexion. 20 mins
Receives: Other: Experimental Myofacial release technique

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Neck Disability Index

    It is a 10-item questionnaire each them of having 6 possible answers. The score of each item lies between 0 to 5, where 0 means no pain/ limitation in activities) and 5 means 'as much pain as possible or maximal limitation in activities'.[19] Thus the Total scores range between 0 - 50 points.

    Measured: 3rd day

  2. Isometric Scapular Pinch Test

    In ISPT the patient actively performs maximal scapular retraction and holds it for 2 seconds. If the pain is present after 15-20 seconds or patient fails to hold it then the test is positive.

    Measured: 3rd day

Secondary outcomes (8)
  1. Lateral Scapular Slide Test

    LSST is a test that assesses the excessive scapular movement with respect to thoracic spine. A total of three measurements are taken in three positions:

    From scapular spine to T2/T3 level From Inferior scapular angle to T7/T9 level From superior scapular angle to T2 level. Measurments are taken 3 times in 3 positions

    Measured: 3rd day

  2. NPRS

    pain is measured with the help of numeric pain rating scale that is 11 point scale from 0-10 with 0 referring no pain and 10 represent max pain.

    Measured: 3rd day

  3. Cervical flexion range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

  4. Cervical extension range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

  5. Cervical Rt side flexion range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

  6. Cervical Lt side flexion range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

  7. Cervical Rt side Rotation range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

  8. Cervical Lt side Rotation range of motion

    The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day.

    Measured: 3rd day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2021
  2. Study start16 Nov 2021
  3. Primary completion1 Jan 2022
  4. Study completion1 Feb 2022

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
None (open label)
Enrolment
66 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05125484
Sponsor's protocol ID
RiphahIU Zainab Rana
Status last verified
Apr 2022
First submitted
8 Nov 2021
Last updated
5 Apr 2022
Results posted
No
Data monitoring committee
Yes
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 experimental Bowen Technique and Experimental Myofacial release technique in people with Trapezius Muscle Strain, 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 5 inclusion and 8 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 5 Apr 2022. 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?

Neck Disability Index (time frame: 3rd day). The study lists 2 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 5 Apr 2022.

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