NCT05502406

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2022

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

August 10, 2022

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 16, 2022

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2023

Completed
Last Updated

August 16, 2022

Status Verified

August 1, 2022

Enrollment Period

10 months

First QC Date

August 10, 2022

Last Update Submit

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

EXPERIMENTAL

The 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

Procedure: Instrument Assisted Soft tissue Mobilization

MMFR

EXPERIMENTAL

The 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

Procedure: Manual Myofascial Release

Interventions

Using a C shaped IASTM tool gentle horizontal stroking at an angle of 45 degree will be given over the cervicodorsal fascia

IASTM

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

MMFR

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: compare two treatment techniques the study type will be parallel experimental study.
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

Locations