Effectiveness of Manual Myofascial Release Versus Instrument Assisted Soft Tissue Mobilization (IASTM) in Patients With Chronic Neck Pain"
1 other identifier
interventional
40
1 country
1
Brief Summary
Neck pain has a global prevalence of 30%, being the fourth leading cause of disability among general population and is more prevalent among females than males, as per concluded by evidence. It is undoubtedly the need of time, to address its proper treatment and to hinder its recurrence amongst the general population. The current physical therapy management of neck pain is more focused towards achieving the short term goals for the patient rather than addressing and amending the actual cause of its relapse. Manual Myofascial Release is one of the very effective treatment used to release soft tissue and fascial adhesions over the myofascia inorder to relieve chronic neck pain. The study aims to compare this manual treatment against Instrument Assisted soft tissue mobilization in order to determine which of the two provides improved outcome in terms of pain, neck disability and cervical Range of motion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2022
CompletedFirst Submitted
Initial submission to the registry
August 10, 2022
CompletedFirst Posted
Study publicly available on registry
August 16, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2023
CompletedAugust 16, 2022
August 1, 2022
10 months
August 10, 2022
August 14, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Pain intensity
Pain will be measured using numeric pain rating scale which is a 10 point scale characterising 0 as no pain and 10 as worst possible pain.
2 weeks
Study Arms (2)
IASTM
EXPERIMENTALThe participants of the respective group will receive myofascial release using a C shaped glider, by the help of gentle horizontal strokes the targeted soft tissue restrictions will be relieved over the cervicodorsal fascia
MMFR
EXPERIMENTALThe participants of the respective group will recieve manual soft tissue release over the cervicodorsal fascia using velvet glove technique for a period of 5 to 7 mins inorder to set free any adhesion in the underlying myofascia
Interventions
Using a C shaped IASTM tool gentle horizontal stroking at an angle of 45 degree will be given over the cervicodorsal fascia
Participants will receive myofascial release through velvet glove technique on upper trapezius and sternocleidomastoid muscle using four strokes in the following fashion: * Begin superior to the clavicle with a loose fist and move the back of the hand over the upper trapezius, fastening the tissue and bringing it over the table. * The next stroke addresses the curve of the neck, again hooking the tissue while moving the bak of your fist towards the table. The last stroke goes over the entire cervical spine hooking over the sternocleidomastoid muscle bringing it into myofascial release. Stay away from the carotid pulse, and incase a pulse is felt, do not apply pressure and reposition your hand
Eligibility Criteria
You may qualify if:
- Male and Female participants belonging to the age group of 18 to 40 years
- Participants suffering from neck pain for more than 3months.
You may not qualify if:
- Recent history of Whiplash Injury.
- Recent traumatic history of head, cervical spine, shoulder girdle or fractures of the cervical spine or shoulder complex.
- History of Cervical Radiculopathy, spondylosis, spondylolisthesis, disc prolapse, any other systemic disease or vascular syndrome such as vertebro-basilar Insufficiency.
- Diagnosed Fibromyalgia, myopathy or myelopathy
- Sensory/Motor dysfunction owing to any neurological pathology in the mid or upper back.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fauji Foundation Hospital
Rawalpindi, Punjab Province, 46000, Pakistan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 10, 2022
First Posted
August 16, 2022
Study Start
March 1, 2022
Primary Completion
January 1, 2023
Study Completion
February 1, 2023
Last Updated
August 16, 2022
Record last verified: 2022-08