Skip to main content
Clinical Trials/CTRI/2024/10/075498
CTRI/2024/10/075498
Not yet recruiting
Not Applicable

Comparison Of Whole-Body Vibration And Sensorimotor Training As Adjunct Therapies For Patients With Non-Specific Chronic Neck Pain: A Randomized Controlled Trial

Jamia Millia Islamia1 site in 1 country33 target enrollmentStarted: October 28, 2024Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
33
Locations
1
Primary Endpoint
Pain intensity

Overview

Brief Summary

The Patients will be recruited from Centre For Physiotherapy and Rehabilitation Sciences. Pateints will be required to sign the consent form explaining their rights as research subjects. All the identifying information on the consent form and demographic data shall be confidential. The initial assessment of the patient will include demographic data, anthropometric characteristics and screening for non-specific chronic neck pain. Baselines assessment will include measurements for neck pain intensity using NPRS, pain pressure threshold using pressure algometer, cervical proprioception using laser pointer mounted onto a lightweight headband, cervical muscle endurance testing using the neck flexor and extensor muscle testing, balance measures using the Pedalosensamove Balance Test and neck function and disability using the neck disability index will be taken. Intervention will be given thrice a week for four weeks. After which post intervention assessment will be taken again.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 50.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Non-specific chronic neck pain since 3 months or longer for less than 7 years Numeric Pain Rating Scale (NPRS) 2-6 Neck Disability Index score- between 5-24 Patients who have a working knowledge of English Willing to participate in the study.

Exclusion Criteria

  • Presence of probable contraindications to vibrations- e.g. pregnancy or recent medical procedure Uncontrolled blood pressure or diabetes History of cervical spine surgery History of head/neck trauma Symptoms of cervical radiculopathy/stenosis Vertebrobasilar insufficiency, vertigo or dizziness from ear or brain disorders eg, BPPV or any other vestibular condition History of whiplash-associated disorders Signs of rheumatic diseases Musculoskeletal or neurological conditions that might affect balance or proprioception Pain reported in the lumbar, hip, knee or ankle at the same time Advanced osteoporosis, pacemaker, arrhythmias Malignancy, infection, or inflammatory disorders Undergoing concurrent treatment for neck pain Difficulty understanding or communicating.

Outcomes

Primary Outcomes

Pain intensity

Time Frame: At baseline and after 4 weeks

Pain Pressure Threshold

Time Frame: At baseline and after 4 weeks

Cervical Proprioception

Time Frame: At baseline and after 4 weeks

Secondary Outcomes

  • Cervical extensor and flexor muscle endurance testing(Balance Measures including static balance, reaction time, proprioception, COP sway, COP range, coordination and multidirectional stability)

Investigators

Sponsor Class
Other [Central University ]
Responsible Party
Principal Investigator
Principal Investigator

Dr Zubia Veqar

Centre For Physiotherapy and Rehabilitation Sciences, Jamia Millia Islamia

Study Sites (1)

Loading locations...

Similar Trials