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Clinical Trials/CTRI/2024/05/066984
CTRI/2024/05/066984Not yet recruitingNot Applicable

Added Effect of Pain Neuroscience Education Combined with Conventional Physiotherapy Treatment versus Conventional Physiotherapy Treatment Alone on Pain and Disability in Patients with Cervical Spondylosis : Assessor-blinded, Quasi Experimental Study.

MAEERs College of Physiotherapy, Talegaon Dabhade1 site in 1 country50 target enrollmentStarted: May 25, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Pain using Numerical Pain Rating Scale

Study Overview

Brief Summary

The World Health Organization (WHO) states that Cervical Spondylosis (CS) is currently regarded as epidemic since neck pain is the second most frequent musculoskeletal illness, right behind low back pain. The cervical spine is especially susceptible to pain, and in two thirds of patients, neck pain develops into a chronic condition that makes it difficult to function and causes considerable agony. 10 to 24% of people are thought to have chronic neck pain.

The effectiveness of PNE as a treatment for chronic pain has been evaluated in a number of research. The first trial, which compared four weeks of PNE and physical therapy (PT) with care provided by regular medical practitioners, was published in 2002. According to the study’s findings, PNE and PT together dramatically decreased pain and impairment both immediately and one year later.

Methodology: Patients selected according to the inclusion criteria will be divided into 2 groups. Group A will include delivery of Pain Neuroscience Education along with Conventional Physiotherapy Treatment (Hot Pack, Neck Isometrics, and Scapular Strengthening) and Group B will be given Conventional Physiotherapy Treatment alone. Data will be collected and analyzed.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Investigator Blinded

Eligibility Criteria

Ages
40.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients with age group 40-60 years Patients diagnosed with chronic cases of Cervical Spondylosis presenting with pain (radiating and/ or non-radiating) and Disability as their chief complaint Patients with chief complaints of Cervical Spondylosis diagnosed by any Orthopedician Patients with a fear factor score above 33, when assessed with FABQ will be selected in the study.

Exclusion Criteria

  • Patients with other Cervical Spine Problems e.g. Inter-vertebral Disc Hernia on Cervical Spine, Spinal Stenosis of the Cervical Region Patients with a History of Cervical Spine over the past year.
  • A history of inflammatory diseases involving neck joints.
  • Myelopathies.
  • A history of Fractures or Dislocations of the Cervical Vertebrae.
  • Patients with any known Psychiatric Disorders will also be excluded.

Outcomes

Primary Outcomes

Pain using Numerical Pain Rating Scale

Time Frame: Baseline and 4 weeks

Secondary Outcomes

  • Disability using Neck Disability Index(Baseline and 4 weeks)

Investigators

Sponsor
MAEERs College of Physiotherapy, Talegaon Dabhade
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Aditi Ramesh Pathak

MAEERs College of Physiotherapy, Talegaon Dabhade

Study Sites (1)

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