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Clinical Trials/CTRI/2024/07/071214
CTRI/2024/07/071214CompletedNot Applicable

Comparative Effects Of Yoga Asanas And Proprioceptive Neuromuscular Facilitation On Pain, Cervical Range, Endurance And Function In Chronic Non-Specific Neck Pain: A Randomized Clinical Trial

KLE Academy Of Higher Education And Research1 site in 1 country36 target enrollmentStarted: August 16, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
36
Locations
1
Primary Endpoint
Neck pain intensity using numerical pain rating scale, Functional ability of neck using neck disability index, cranio-cervical flexion test using chattanooga pressure biofeedback, assessment of cervical range of motion using universal goniometer

Study Overview

Brief Summary

COMPARATIVE EFFECTS OF YOGA ASANAS AND PROPRICEPTIVE NEUROMUSCULAR FACILITATION ON PAIN, CERVICAL RANGE, ENDURANCE AND FUNCTION IN CHRONIC NON-SPECIFIC NECK PAIN: A RANDOMIZED CLINICAL TRIAL.

Aim of the study- To assess and compare the effect of yoga asanas vs PNF on pain, cervical range, endurance and function in participants with chronic non-specific neck pain.

Null hypothesisH0- There will be no difference in the effect of yoga asanas and PNF on pain, cervical range, endurance, and function in chronic non-specific neck pain.

Alternate hypothesis-There will be difference in the effect of yoga asanas and PNF on pain, cervical range, endurance and function in chronic non-specific neck pain.

Inclusion criteria-Both male and female, participants aged between 18-50 years, participants having chronic non specific neck pain with duration of more than 12 weeks, participants having neck pain with intensity from 2-6 on numerical pain rating scale, participants willing to participate in the study.

Exclusion criteria-participants having history of injury, tumour or infections in the cervical region, participants having history of fracture of upper and lower limb and spine, participants who has history of whiplash injury, participants diagnosed with osteoporosis, osteoarthritis, rheumatoid arthritis, participants diagnosed case of psychological deficit.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • Both male and female
  • Participants aged between 18-50 years
  • Participants having chronic Non-specific neck pain with duration of more than 12 weeks
  • Participants having neck pain with intensity ranging from 2-6 on numerical pain rating scale.
  • Participants willing to participate in the study.

Exclusion Criteria

  • Participants with history of injury, tumour or infections in the cervical region.
  • Participation having history of fracture of upper and lower limb and spine.
  • Participants who has the history of whiplash injury.
  • Participants diagnosed with osteoporosis, osteoarthritis, rheumatoid arthritis.
  • Participants diagnosed case of psychological deficit.

Outcomes

Primary Outcomes

Neck pain intensity using numerical pain rating scale, Functional ability of neck using neck disability index, cranio-cervical flexion test using chattanooga pressure biofeedback, assessment of cervical range of motion using universal goniometer

Time Frame: Pre assessment will be taken before giving the intervention and post assessment will be done after 4 weeks of intervention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
KLE Academy Of Higher Education And Research
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Shivani Patil

KAHER Institute of Physiotherapy

Study Sites (1)

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