Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06656182

Effect of SNAGs and Scapular Mobilizations in Patients With Scapulocostal Syndrome

To determine the impact of SNAGs and Scapular mobilizations on pain, cervical and shoulder Range of motion and functional outcomes in individuals with Scapulocostal Syndrome.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

DSK physio and Rehab Center

Rawalpindi, Punjab Province, 44000, Pakistan

Location status: Recruiting

Location contact

Asmar Fatima, MS-OMPT

CONTACT

[email protected]

03336195644

Asmar Fatima, MS-OMPT

SUB_INVESTIGATOR

Rabia Asif, MS_OMPT*

CONTACT

[email protected]

03335193218

Rabia asif, MS-OMPT*

PRINCIPAL_INVESTIGATOR

About this study

The rationale for employing SNAGS (Sustained Natural Apophyseal Glides) in treating scapulocostal syndrome is multifaceted. By targeting specific joint surfaces and soft tissue structures, SNAGS aim to address joint dysfunction, alleviate pain, and improve mobility in the scapulothoracic region. These sustained gliding movements not only modulate pain signals but also promote relaxation and reduce muscle tension, thereby enhancing the effectiveness of therapeutic exercises aimed at strengthening the surrounding musculature. Additionally, SNAGS facilitate proper muscle activation patterns, optimizing muscle function and coordination. Their adaptability allows for a patient-centered approach, ensuring tailored treatment that considers individual symptoms, mobility deficits, and treatment goals, ultimately promoting better functional outcomes in individuals with scapulocostal syndrome.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age- 18 to 40 years.
  • Male and female both
  • Nonspecific neck pain with a duration of greater than 3 months
  • No pain reproduction on isometric muscle testing in shoulder.
  • Patients who could not achieve 60 degrees of upward rotation when elevating the arms above the head i.e. presence of scapular dyskinesia
  • pain with a referral pattern while receiving manual pressure of at least 3 points on the medial scapular muscles (levator scapulae, rhomboid major, rhomboid minor, and serratus posterior superior) evaluated through Travels and Simon criteria.
  • Discomfort, pain, or limitations in neck extension, neck rotation bilaterally, shoulder forward flexion, shoulder abduction attributed to SCS.
  • Willing to provide informed consent to participate in the study.

Exclusion criteria

  • Musculoskeletal pathologies affecting the cervical spine or lower extremities (e.g., herniated disc, cervical radiculopathy, cervical stenosis, shoulder labral tear).
  • history of degenerative shoulder joint disease
  • rotator cuff dysfunction
  • Thoracic outlet syndrome
  • Brachial neuralgia
  • shoulder impingement syndrome
  • adhesive capsulitis
  • Pregnant individuals due to potential discomfort.
  • Open wounds, infections, or skin conditions at pain site.

Treatment and study plan

Cervical and Thoracic SNAGs

Other

cervical SNAGs (C3-C7) and thoracic SNAGs (T1-T12) with 6 repetitions of 1 set three times per week for 4 weeks along with scapular mobilizations of 10 repetitions of 1 set and stretching of trapezius (upper, middle and lower fibers), levator scapulae and rhomboids (major and minor)

traditional physical therapy and scapular mobilizations

Other

scapular mobilizations of 10 repetitions of 1 set and stretching of trapezius (upper, middle and lower fibers), levator scapulae and rhomboids (major and minor)

Primary outcomes

  1. Neck disability index

    Time frame: 4th week

    changes from baseline The Neck Disability Index (NDI) serves as a valuable tool for evaluating neck pain issues, drawing on the framework of the Oswestry index for back pain and the Pain Disability Index. Its effectiveness lies in its focus on the impact of neck pain on daily activities, reflecting the specific concerns and experiences of individual patients.

    Comprising 10 sections, each containing 5 questions related to affected activities, the index allows patients to select the response that best represents their situation, with scores ranging from 0 to 5.

Secondary outcomes

  1. NPRS

    Time frame: every week

    changes from baseline Pain through NPRS at the end of every week for 4 weeks

  2. Cervical and Shoulder ROM

    Time frame: every week

    changes from baseline at the end of every week till last week

Study contacts

Contact information is provided by the study sponsor or research team.

Asmar Fatima, MS-OMPT

CONTACT

[email protected]

03336195644

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 24, 2024
Registry last updated
Oct 24, 2024

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.