- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05092334
Effect of Proprioceptive Exercises on Pain and Function in Non-specific Chronic Neck Pain
This study was conducted to see the effect of proprioceptive exercises on pain and function in Non-specific chronic neck pain.
Twenty participants with chronic Non-specific neck pain were enrolled in this study. During the final week of treatment, 14 patients were assessed at the end of the sixth treatment week. Participants were randomized into two groups treatment group and control group. Both groups were treated with conventional treatment which were strengthening exercises. Treatment group was also treated by proprioception exercises. For measurement of pain and disability NPRS and NDI scales were used. Exercise regime distributed in six weeks period one session per week exercise, 10-12 repetitions with 1-minute rest interval, lasted 45 minutes in both groups. pre-treatment and post-treatment measurements were taken.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
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Lahore, Punjab, Pakistan, 54000
- Qurat ul Ain
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with non-specific neck pain>3 months
- Postural neck pain
Exclusion Criteria:
- Vascular neoplasia
- Fibromyalgia
- Rheumatoid arthritis
- Radiculopathy
- Neuropathy
- Tumor
- Cervical fractures
- Vestibular problems
- Congenital disorder of cervical spine
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Proprioceptive exercises
Group A treated with proprioceptive exercises. proprioception exercises included.
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proprioception exercises included (a)Head relocation it involve the practice of relocating head back to natural head posture and to predetermined positions in range first with eyes open using feedback from a laser attached to their head and then with closed all active movement of cervical flexion extension lateral flexion and rotations were used.(b)Gaze
stability oculomotor exercises commencing with eyes movement with the head stationary ,progressing to movement of head with visual fixation on a target.
(c) Eye head coordination exercises, commenced with rotation of eyes and head to the same side in both right and left directions.
Then progressed with both eyes and head move in opposite direction
|
|
Experimental: Strengthening exercises
Group B treated with strengthening exercises which are performed with prone and supine position by placing a towel under head, press towel for 5 seconds with 10-12 repetitions ,one set in a week for six weeks for cervical muscles
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strengthening exercises which are performed with prone and supine position by placing a towel under head, press towel for 5 seconds with 10-12 repetitions ,one set in a week for six weeks for cervical muscles
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numerical pain rating scale
Time Frame: 6 weeks
|
11 point numeric scale ranges from 0 representing one pain extreme(no pain)to 10 representing the other pain extreme severity
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NECK DISABILITY INDEX
Time Frame: 6 weeks
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NDI is ten item questionnaire based on Oswestry low back pain that assess disability associated with neck pain and whiplash.
There are four items that relate to symptoms(pain intensity ,headache, concentration ,sleeping)and six items that relate daily activities of life(lifting, work, driving, recreation, personal care, reading) 5-14 score :mild disability,15-24 score moderate disability,25-34 score severe disability,>35 complete disable
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Qurat ul Ain, Mphil, Riphah International University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/Lhr//2043 Noshaba kanwal
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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