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Clinical Trials/NCT05777408
NCT05777408
Completed
Not Applicable

Additional Effect of Cranial Base Release on Cervical Range and Proprioception in Patients With Mechanical Neck Pain

Foundation University Islamabad1 site in 1 country20 target enrollmentJanuary 1, 2023
ConditionsNeck Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck Pain
Sponsor
Foundation University Islamabad
Enrollment
20
Locations
1
Primary Endpoint
Change in Pain
Status
Completed
Last Updated
8 months ago

Overview

Brief Summary

Mechanical Neck pain is the second most commonly occurring musculoskeletal disorder worldwide, ranking 4th in overall disability. It is referred to as Nonspecific generalized neck pain with mechanical characteristics with a primary location between the supranuchal line and the first thoracic spinous process, includingpatients suffering from mechanical neck pain are reported to have several impairments, including pain, reduced cervical ROM, neck disability, and proprioceptive dysfunction. The treatment indicated involves the use of electrotherapy and thermal modalities. In addition, the use of different manual therapy techniques is advocated; however, the most effective management is still debatable. Evidence suggests that Natural Apophyseal glides have a significant positive effect on mechanical neck pain patients. So the study will identify the additional effect of cranial base release with natural apophyseal glides in alleviating pain and its effects on proprioception.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
July 1, 2023
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with mechanical neck pain having reproducible non-specific neck pain with a primary location between the supranuchal line and the first thoracic spinous process
  • Male and Female
  • Age 18-40 years
  • Pain severity on NPRS \>3
  • Neck Disability score of 20% or above
  • Problem not older than 2 months

Exclusion Criteria

  • Patients with history of
  • Recent significant trauma (including whiplash)
  • Radiculopathy
  • Cervical fracture
  • Neck surgery
  • Dizziness, vertigo
  • Myelopathy, Malignancy
  • Metabolic disease
  • Diagnosed Osteoporosis, Rheumatoid arthritis
  • Long-term corticosteroid and/or painkiller drug use

Outcomes

Primary Outcomes

Change in Pain

Time Frame: 2 weeks

Pain will be measured on Numeric Pain Rating Scale.

Change in ROM

Time Frame: 2 weeks

Cervical rotation will be measured through CROM device

Change in Cervical Proprioception

Time Frame: 2 weeks

Will be measured from Laser Pointer Method

Study Sites (1)

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