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NCT Number: NCT06998615

Correlation Between Shoulder Impingement and Cervical Proprioception

this study will be conducted to evaluate the correlation between shoulder impingement and cervical proprioception

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Key information

Age range

25 year–45 year

Sex eligibility

All sexes

Study type

Observational

About this study

Shoulder pain is one of the most common complaints in musculoskeletal practice, whether it comes from impingement syndrome or a defect in rotator cuff muscles .Shoulder pain is considered to be the third most common complaint in musculoskeletal practice, with a prevalence of 7% to 34% .Shoulder impingement is a syndrome where there is entrapment of soft tissue through the shoulder joint, with a prevalence of 44% to 65% of all shoulder complaints. Shoulder impingement has multiple causes, whether functional, degenerative, and anatomical and mechanical causes .Shoulder impingement classified to primary and secondary. Secondary impingement is subdivided into internal and external impingement .Proprioception components are joint position sense, kinesthesia, sense of force, sense of change of velocity. joint position sense is our perception of position of the joint or limb it divided to active/passive joint position sense, it means that the person can relocate the position of the joint or the limb to the same position after the joint or limb is moved.the muscle receptor helping in identifying the limb position and movement through changeling in neural signaling in the sensory receptor, giving the neurological control and basis of proprioception to sensory receptors located in the skin, muscles, and joints, so the proprioception is considered to be a loop of feedforward and feedback signals between sensory receptor and the nervous system. sixty eight subjects with shoulder impingement syndrome will be joined to this study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis: Patients diagnosed with shoulder impingement
  • Age: Patients aged between 25 and 45 years.
  • Pain and mobility issues: Patients must report mild to moderate pain and/or restricted range of motion (ROM) in shoulder joint .
  • Ability to provide informed consent: Participants must be able to understand the study protocol and provide written informed consent to participate.
  • Medical stability: Patients must be medically stable and able to engage in physical assessment

Exclusion criteria

  • any patient aged below 25 or above 45 years old
  • Subjects have malignancy: Patients with severe neurological, musculoskeletal, disorders that could interfere with the study interventions
  • Subjects have history of shoulder trauma, fractures and surgeries:
  • Subjects have neck dysfunction
  • Cognitive impairment: Patients with significant cognitive impairment or mental health conditions that would hinder their ability to understand or comply with the study protocol.

Treatment and study plan

shoulder impingement group

Other

the Patients with shoulder impingement syndrome in this group had at least 3 out of the following 6 criteria 1) positive "Neer's sign"; 2) positive "Hawkins' sign"; 3) pain on active shoulder elevation in the scapular plane, 4) pain on the C5-C6 dermatome; 5) pain on palpation of the rotator cuff tendons and 6) pain with resisted isometric abduction.

normal subjects

Other

the subjects in this group had no pain or disability in shoulder

Primary outcomes

  1. joint position error (cervical proprioception)

    Time frame: up to thirty minutes

    neck proprioception by Joint Position Error (JPE) using LASER beam Point tool and it's conducted as patient sitting 90 cm away from the target map on the wall ad a light weight headband with laser pointer is placed on the patient head, the patient is asked to focus on the center of the map while eye open then the patient asked to close his eyes and move his head in one plane and back to the starting point as accurately as possible and indicate verbally that he back to the starting position before opening his eyes, he repeated for 6 times in each plane and the distance between the starting point and the ending point is measured and then converted to degrees the patient is diagnosed to has a proprioception deficit if the mean error of any direction in more than 4.5 degrees

  2. shoulder disablity

    Time frame: up to thirty minutes

    The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use.he pain scale is summed up to a total of 50 while the disability scale sums up to 80. The total SPADI score is expressed as a percentage. A score of 0 indicates best 100 indicates worst.

  3. pain intensity

    Time frame: up to thirty minutes

    Pain will be assed with numerical analog scale (NPRS) in which a respondent selects a whole number (0-10 cm) that best reflects the intensity of his/her pain. 0 mean no pain and 10 mean maximum pain

Study contacts

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

mustafa basha, master

CONTACT

[email protected]

01064441563

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Acronym: CP

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 31, 2025
Registry last updated
Jun 4, 2025

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.

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