Skip to main content
OpenTrials
Completed

NCT Number: NCT06907459

Effect of Release of Upper Track of Deep Front Facial Line Versus Myofascial Release With IASTM on Patients With Upper Cross Syndrome

this study will be conducted to compare the effect of release of upper track of deep front facial line versus myofascial release with IASTM on patients with Upper Cross Syndrome.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alshaymaa Shaaban Abdelazeim

Giza, Dokki, 11351, Egypt

About this study

Upper cross syndrome is a postural dysfunction that can cause a variety of upper-body musculoskeletal problems. Early detection and physiotherapy can help to prevent further complications. Maintaining bad posture over an extended duration can cause postural dysfunction and misalignment.

The first and most obvious sign of upper crossed syndrome is the characteristic postural dysfunction of protracted scapulae, medially rotated humeri, hyperkyphotic upper thoracic spine, and a protracted/ anteriorly held head, which is created by hypo lordosis or even kyphosis (excessive flexion) of the lower cervical spine, hyper lordosis of the upper cervical spine and head, and anterior translation of the head upon the atlas.

The available treatments for upper cross syndrome are Stretching, strengthening, myofascial release, postural relaxation exercise, electrical stimulations, and deep neck flexors activations are the most used techniques. Numerous studies have highlighted various benefits in terms of time efforts, and prognosis. Those are corrective exercise, Kinesio taping, scapular stabilization exercise, and PNF techniques.

Studies have demonstrated the role of fascia in various musculoskeletal dysfunctions as the fascial tissues connect the skeletal muscles forming a body-wide web in a pattern called myofascial meridians. As fascia is able to modify its tensional state, strain transmission along the meridians might occur in response to changes in muscle activity.

Deep fascia tends to be highly vascularized and contain well developed lymphatic channels. In some instances, deep fascia can even contain free encapsulated nerve endings, such as Ruffini and Pacinian corpuscles. It is present in our body in different tissue planes and in different forms with specific function and the musculoskeletal fascial system can be affected by various localized disorders with variable time course and prognosis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18-40 years old
  • All participants had forward head, craniovertebral angle < 50.
  • All participants had rounded back (kyphosis angle ≥ 42°)
  • Based on assessment of upper cross syndrome by photogrammetric analysis.
  • The subjects were chosen from both genders.

Exclusion criteria

  • History of trauma or surgery in cervical region.
  • Bone fractures or acute soft tissue injuries.
  • Osteoporosis.
  • Heart attack.
  • Unstable angina pectoris -Implanted pacemaker or defibrillator- -Cancer-
  • Rheumatoid arthritis
  • Connective tissue disease: This includes diseases such as osteomyelitis, lupus and scleroderma -Neurological conditions-

Treatment and study plan

upper Track of Deep Front Facial Line realese

Other

The MFR techniques were applied to the designated regions, with soft, steady pressure lasting 90 to 120 seconds postural correction exercises The upper track of deep front facial line release procedures were applied. Hyoid mobilization; Larynx mobilization; Sternal oscillations; and Barral's Transversus Thoracis mobilization. The thoracic inlet releasing ; intrathoracic fascia elongation; scalene releasing and diaphragm relaxation

Myofascial Release With IASTM

Other

The instrument is designed to mobilize soft tissues. Facilitation approaches were employed to break apart adhesions. Emollient Gel/Lubrication Gel (Hawk Grips product) was also used to lubricate the skin and allow the instrument to move more easily. The tool has two sides: one for therapy and the other for holding plus postural correction exercises

supervised corrective exercises

Other

The exercise program included cervical stabilization exercises performed in 3 sets of 10 repetitions with a 10-second maintenance, scapular stabilization exercises plus stretching of cervical muscles.

Primary outcomes

  1. neck disability

    Time frame: up to four weeks

    The neck disability assessment will be performed using the Neck Disability Index (NDI) questionnaire - it contains ten items that refer to neck pain (intensity) and the level of ability to manage daily living activities (personal care, reading, lifting, headache, work, concentration, driving, sleep and recreation). The NDI score is interpreted as 0-4=no disability, 5-14=mild disability, 15-24=moderate disability, 25-34=severe disability, and over 34= total disability, where a score of 50 converted to percentiles represents 100%. NDI score is calculated as follows: total score/total possible score, transformed to percentage multiplied by 100=% points

Secondary outcomes

  1. pain intensity

    Time frame: up to four weeks

    he subject was in a relaxed position then gave him the appendix which contains VAS. The subject was instructed to place a vertical mark on the line to indicate his/her pain. the line has two ends; one with no pain (zero) and the other extreme pain (100 mm) at the other end

  2. craniovertebral angle

    Time frame: up to four weeks

    craniovertebral angle will be measured by Photogrammetry method. A CVA below 48-50 degrees indicates FHP

  3. kyphosis angle

    Time frame: up to four weeks

    kyphosis angle will be measured by Photogrammetry method.

  4. upper chest expansion

    Time frame: up to four weeks

    tape measurements will be used to measure upper chest expansion

  5. lower chest expansion

    Time frame: up to four weeks

    ape measurements will be used to measure lower chest expansion

  6. cervical range of motion

    Time frame: up to four weeks

    cervical range of motion device will be used to measure cervical range of motion

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Acronym: UCS

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 2, 2025
Registry last updated
Feb 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.