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Cairo UniversityCorrelation Between Shoulder Impingement and Cervical Proprioception (CP) 68
Clinical Trial NCT06998615 (CP) is an observational study for Shoulder Impingement and is currently not yet recruiting. Enrollment is planned to begin on 30 May 2025 and continue until the study accrues 68 participants. Led by Cairo University, this study is expected to complete by 30 July 2025. The latest data from ClinicalTrials.gov was last updated on 4 June 2025.
Brief Summary
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 6...Show More
Official Title
Correlation Between Shoulder Impingement and Cervical Proprioception
Conditions
Shoulder ImpingementOther Study IDs
- CP
- P.T.REC/012/005804
NCT ID Number
Start Date (Actual)
2025-05-30
Last Update Posted
2025-06-04
Completion Date (Estimated)
2025-07-30
Enrollment (Estimated)
68
Study Type
Observational
Status
Not yet recruiting
Keywords
shoulder impingement
neck proprioception
correlation
cervical proprioception
neck proprioception
correlation
cervical proprioception
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
shoulder impingement group thirty four subjects with shoulder impingement will be included in this group | 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. |
normal subjets thirty four normal subjects will be included in this group | normal subjects the subjects in this group had no pain or disability in shoulder |
Primary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
joint position error (cervical proprioception) | 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 | up to thirty minutes |
shoulder disablity | 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. | up to thirty minutes |
pain intensity | 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 | up to thirty minutes |
Participation Assistant
Eligibility Criteria
Eligible Ages
Adult
Minimum Age
25 Years
Eligible Sexes
All
- 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
- 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.
Cairo University1117 active studies to exploreStudy Responsible Party
Mustafa Yahia Abdelaziz Ebrahim Basha, Principal Investigator, principle investigator : mostafa yahia abdelaziz ibrahim, Cairo University
Study Central Contact
Contact: mustafa basha, master, 01064441563, [email protected]
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