- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06353802
Relationship Between Chronic Non-Specific Neck Pain And Lumbar Reposition Sense
Correlation Between Chronic Non-specific Neck Pain and Lumbar Reposition Sense: a Correlative Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Around 67% of people on the planet may at some point in their lives experience chronic, non-specific neck pain. People who have chronic pain frequently need medical services and medications for pain treatment, and there is a link between their functional limitations and disabilities.
Cervical pain without a recognized clinical reason for the complaints is classified as chronic non-specific neck pain. Some symptoms include weakening in the neck muscles and reduced mobility of the cervical spine.
"Pain perceived anywhere in the posterior region of the cervical spine, from the superior nuchal line to the first thoracic spinous process" is how the International Association for the Study of Pain (IASP) characterized chronic non-specific neck pain.
Individuals who experience unilateral or central neck discomfort are said to have persistent non-specific neck pain. There will be restricted range of motion in the neck, which frequently re-creates the symptoms; referred shoulder girdle or upper extremity pain may also be felt. Patients may also get cervicogenic headaches (CGH).
Spine position, stability, and movement are all governed by motor control, which results from the ongoing interaction of sensory inputs, such as proprioception, on different neural system levels, and motor outputs to effectors, such as paraspinal muscles.
The capacity to precisely position the trunk at predefined points along the sagittal plane's range of motion is known as trunk position sense. Trunk repositioning protocols may be a valuable tool for measuring trunk control since they demand that participants precisely move and control the flexing trunk.
The most popular criterion for assessing proprioceptive senses is joint repositioning errors. By first generating a target angle or joint location using position or movement sensors, then having the subject represent that place, the test examines the discrepancy between the initial target location and the location realised by the subject.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Giza, Egypt, 12613
- Physical Therapy College Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male and female patients,18-50 years old
- Neck pain continued for at least the last 12 weeks
- Normal Body mass index ranged from 18.5 to 24.9
Exclusion Criteria:
- Radiated neck pain
- Neck pain associated with vertigo
- A history of surgery on the lower limbs or back
- Back or lower extremity trauma within the last three months.
- neurological or vestibular disorders
- Diagnosed psychological disorders
- Vertebral fractures
- Metal spine implants
- Tumors
- Diagnosed metabolic diseases
- Using medications that could have an impact on balance in the 24 hours before to the study
- Previous neck surgery
- Red flags (night pain, severe muscle spasms, sudden loss of weight)
- Physiotherapeutic treatment continued in the last 3 months
- Pregnancy, including six months postpartum
- A diagnosed psychiatric disorder or severe cognitive impairment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Other: group 1
Participants will be measured using iPhone® Inclinometer Application.
The measurement app level, a measuring tool, was utilised with the iPhone® 10 (Apple Inc., California, USA).
A free application that is built into the iPhone®, The measurement app level shows the numerical size in a manner similar to a digital inclinometer.
The programme shows the angle measured using a digital display and the accelerometer included into the iPhone®.
Degrees (°) were used as the measurement unit.
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In order to evaluate the lumbar joint repositioning error using the Joint Positioning Sense, the following guidelines were followed: (I) The participants were to stand with their arms at their sides, their feet externally rotated (about 20 degrees). (II) With the feet flat on the floor and the arms resting on the front of the thighs, the person was seated in a height-adjustable seat that measured the length of the shank. (III) With a belt fastened, the iPhone® was positioned upright just above the iliac crest, (IV) the inclination of the inclinometer was 0°; (V) The inclinometer's 0° point was set as the initial position. (VI) The individual was passively guided by the assessor to a 30° flexion within the range of 0 to 30°; (VII) the subject was to memorize this position for 10 s; (VIII) the subject actively returned to the initial position. (IX) Subsequently, the participant was required to actively replicate the position three times. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation Between Chronic Non-Specific Neck Pain And Lumbar Reposition Sense Using iPhone inclinometer app
Time Frame: one month
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using the iPhone inclinometer app to asses the lumbar reposition error measures with degrees and it's correlation to cervical non-specific neck pain using visual analogue scale ranging from 1 to 10
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one month
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004963
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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