Intervention group
OtherGroup/Cohort Description: Participants with Upper Cross Syndrome (UCS) who undergo the prescribed exercise or treatment protocol.
NCT Number: NCT06801613
Correlation Between Upper Cross Syndrome and Neck Proprioception
Hypothesis:
No statistically significant relationship exists between upper cross syndrome and neck proprioception.
Study Design:
Randomized Controlled Trial
Participants:
Office workers (≥4h computer use/day) Age: 28-48 years Chronic nonspecific neck pain (>3 months) Forward head posture (FHP) <46° VAS score: 3-8 cm No cognitive impairments affecting participation
Exclusion Criteria:
Systemic, rheumatic, or neuromuscular diseases Neurological signs, spinal surgery, or recent physical therapy Missing ≥3 consecutive or 4 nonconsecutive sessions
Trial opening soon.
Get Notified28 year–48 year
All sexes
Observational
Study Title:Correlation Between Upper Cross Syndrome and Neck Proprioception
Hypothesis:There will be no statistically significant relationship between upper cross syndrome and neck proprioception.
Methodology:
Study Design:Randomized controlled trial
Inclusion criteria
Office workers using a computer for at least 4 hours daily
Aged between 28 and 48 years
Neck pain (NP) between 3 and 8 cm on a visual analog scale (VAS) (0 = no pain, 10 = unbearable pain)
Chronic nonspecific neck pain lasting for more than 3 months
Forward head posture (FHP) less than 46°
Patients willing and able to participate in an exercise program safely without cognitive impairments that would limit participation
Exclusion criteria
Specific causes of NP (e.g., systemic, rheumatic, neuromuscular diseases)
Central or peripheral neurological signs
Cognitive impairment
History of spinal surgery
Physical therapy treatments in the last 6 months prior to baseline assessment
Participants missing at least three consecutive or four nonconsecutive sessions
Outcome Measures:
Spinal Curvature Assessment Using Spinal Mouse DeviceThe spinal mouse device is physically guided along the skin of the spine
Neck Pain MeasurementNP is evaluated using a 10-cm VAS, a widely used clinical tool for assessing pain treatment effectiveness.
Neck Disability Index (NDI)Disability is assessed using the NDI questionnaire.
Measurement of Cervical Range of Motion (CROM) Using a CROM
Assessment of Cervical Proprioception Using the CROM DeviceHead Reposition Accuracy Tests:
Neutral Head Position (NHP) Test: Measures the ability to actively reposition the head to the self-selected neutral position.
Target Head Position (THP) Test: Measures the ability to actively reposition the head to a previously demonstrated target position.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Group/Cohort Description: Participants with Upper Cross Syndrome (UCS) who undergo the prescribed exercise or treatment protocol.
Time frame: 8 weeks
Measurement Tool: CROM device.
Tests:
Neutral Head Position (NHP): Assesses participants' ability to actively reposition their head to a self-selected neutral position.
Target Head Position (THP): Assesses ability to reposition the head to a previously demonstrated target position.
Time frame: 8 weeks
Measurement Tool: Visual Analog Scale (10-cm scale)
Purpose: Evaluate participants' subjective pain levels before and after the intervention.
Scale Range: 0 (no pain) to 10 (unbearable pain). Interpretation: Higher scores indicate worse pain levels.
Time frame: 8 weeks
Measurement Tool: Biodex Balance System.
Parameters:
Static and dynamic balance. Postural stability score (lower scores indicate better balance). Purpose: Explore the effect of UCS on overall balance and stability.
Time frame: 8 weeks
Measurement Tool: NDI questionnaire. Purpose: Assess the impact of neck pain on daily activities and functional limitations.
Time frame: 8 weeks
Measurement Tool: CROM device. Purpose: Measure the range of motion in the cervical spine to detect restrictions due to UCS.
Time frame: 8 weeks
Measurement Tool: Spinal Mouse Device.
Parameters:
Sagittal plane alignment in neutral, flexion, and extension.
Purpose: Assess structural changes or adaptations in the spine due to UCS.
Contact information is provided by the study sponsor or research team.
Cairo University
Other
Correlation Between Upper Cross Syndrome and Neck Proprioception
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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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