Upper Cross Syndrome and Neck Proprioception
Correlation Between Upper Cross Syndrome and Neck Proprioception
1 other identifier
observational
80
0 countries
N/A
Brief 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2025
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 25, 2025
CompletedFirst Posted
Study publicly available on registry
January 30, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 25, 2025
CompletedJanuary 31, 2025
January 1, 2025
3 months
January 25, 2025
January 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Cervical Proprioception:
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.
8 weeks
Secondary Outcomes (4)
Neck Pain
8 weeks
Balance
8 weeks
Neck Disability Index (NDI):
8 weeks
Cervical Range of Motion (CROM)
8 weeks
Other Outcomes (1)
Spinal Curvature:
8 weeks
Study Arms (1)
control group
Participants with UCS who do not receive the intervention (e.g., may receive standard care, education, or no treatment).
Interventions
Group/Cohort Description: Participants with Upper Cross Syndrome (UCS) who undergo the prescribed exercise or treatment protocol.
Eligibility Criteria
The study population consists of adult office workers with specific characteristics related to their occupation, posture, and neck pain history. Below is a detailed breakdown: Demographic Characteristics Age Range: 28-48 years. Gender: Not specified, but likely includes both males and females. Occupation: Office workers using computers for at least 4 hours daily. Clinical Characteristics Chronic Nonspecific Neck Pain (CNP): Pain lasting ≥3 months. Pain intensity between 3-8 cm on the Visual Analog Scale (VAS). Forward Head Posture (FHP): Measured angle of FHP is less than 46°. No Specific Diagnoses: Participants with neck pain due to systemic, rheumatic, or neuromuscular diseases are excluded.
You may qualify if:
- office workers (using a computer at least 4 h),
- aged between 28 and 48 years,
- NP between 3 and 8 cm on a visual analog scale (VAS) (from 0 indicating no pain at all to 10 indicating unbearable pain),
- chronic nonspecific neck pain lasting for more than 3 months, and FHP less than 46° (Fathollahnejad et al., 2019).
- Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation.
You may not qualify if:
- specific causes of NP (e.g., systemic, rheumatic, neuromuscular diseases), central or peripheral neurological signs, cognitive impairment, spinal surgery, or physical therapy treatments in the last 6 months prior to the baseline assessment.
- Participants would be also excluded if they missed at least three consecutive or four nonconsecutive sessions (Fathollahnejad et al., 2019).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 8 Weeks
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- general practitioner
Study Record Dates
First Submitted
January 25, 2025
First Posted
January 30, 2025
Study Start
May 1, 2025
Primary Completion
July 25, 2025
Study Completion
October 25, 2025
Last Updated
January 31, 2025
Record last verified: 2025-01