Trials / Not Yet Recruiting
Not Yet RecruitingNCT06801613
Upper Cross Syndrome and Neck Proprioception
Correlation Between Upper Cross Syndrome and Neck Proprioception
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 80 (estimated)
- Sponsor
- Cairo University · Academic / Other
- Sex
- All
- Age
- 28 Years – 48 Years
- Healthy volunteers
- Not accepted
Summary
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
Detailed description
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Intervention Group | Group/Cohort Description: Participants with Upper Cross Syndrome (UCS) who undergo the prescribed exercise or treatment protocol. |
Timeline
- Start date
- 2025-05-01
- Primary completion
- 2025-07-25
- Completion
- 2025-10-25
- First posted
- 2025-01-30
- Last updated
- 2025-01-31
Source: ClinicalTrials.gov record NCT06801613. Inclusion in this directory is not an endorsement.