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Effect of multimodal rehabilitation on hand functions in chronic neck pai

Phase 2
Conditions
Health Condition 1: M999- Biomechanical lesion, unspecified
Registration Number
CTRI/2023/06/053588
Lead Sponsor
Jamia Hamdard
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Clinically diagnosed subjects with chronic neck pain.

2.Chronic neck pain having not less than 3 cm on Visual Analogue Scale causing pain, impairment of function and physical disability

3.Subjects with either local spinal pain or joint stiffness or combination of both between C3- C7 with no radiating pain in the upper limbs.

4.Only the subjects who gave written informed consent will be included in the study.

Exclusion Criteria

1.Subjects with a diagnosed cervical radiculopathy or any nerve root involvement.

2Subjects with a history of osteoporosis

3.Subjects having undergone neck surgery during the past twelve months.

4.Subjects with uncontrolled diabetes with and without peripheral neuropathy.

5.Subjects with diagnosed vestibular, balance impairments.

6.Recent history of injury or trauma to the upper limb.

7.Subjects having any drug abuse

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain, <br/ ><br>Neck Posture <br/ ><br>Muscle Thickness <br/ ><br>Muscle Endurance <br/ ><br>Grip strength <br/ ><br>Hand function <br/ ><br>Pinch strength <br/ ><br>Timepoint: At baseline, at the end of 4 weeks and at the end of 8 weeks.
Secondary Outcome Measures
NameTimeMethod
eck Range of Motion <br/ ><br>Neck Disability IndexTimepoint: The outcome measures will be recorded at the end of every 2 weeks of intervention and on the completion of intervention.
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