Correlation Between Shoulder Impingement and Cervical Proprioception
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: shoulder impingement group, normal subjects.
- Who it may be relevant to
- Registry conditions: Shoulder Impingement. Basic parameters: 25 years — 45 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
this study will be conducted to evaluate the correlation between shoulder impingement and cervical proprioception
Detailed description
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.
Interventions
- Other shoulder impingement group
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. - Other normal subjects
the subjects in this group had no pain or disability in shoulder
Primary outcome measures
- joint position error (cervical proprioception) [Time frame: up to thirty minutes]
- shoulder disablity [Time frame: up to thirty minutes]
- pain intensity [Time frame: up to thirty minutes]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06998615 · P.T.REC/012/005804