- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05884567
Effectiveness of Neck Isometric Exercises and Cervical Mobilization on Cervical Radiculopathy
May 22, 2023 updated by: Neuro Counsel Hospital, Pakistan
Effectiveness of neck isometric exercises and cervical mobilization will be compared to observe the efficacy of these techniques on cervical radiculopathy
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Two groups will be formed to observe the efficacy of neck isometric exercises and cervical mobilization on cervical radiculopathy by using NPRS, ROM and QoL tools.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Federal
-
Islamabad, Federal, Pakistan, 44010
- Al Nafees Medical Hospital, Islamabd
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Males and females with age between 25-50 years
- Patients referred from neuro and orthopedic departments with diagnosed cervical radiculopathy.
- Complaint of neck pain on neck bending with positive spurling's test.
- Complaint of neck pain, numbness and tingling in arm with positive spurling's test.
Exclusion Criteria:
- Cervical Trauma
- Any other orthopedic and neurological conditions of cervical spine.
- Fracture
- Malignancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental
neck isometric exercises will be administered at for 4 weeks and will be evaluuated at baseline, 2nd and after 4 weeks of interventions
|
These exercises are used to increase muscle endurance, power and ROM
|
|
Active Comparator: control
cervical mobilization will be administered at for 4 weeks and will be evaluuated at baseline, 2nd and after 4 weeks of interventions
|
These exercises are used to increase ROM and used for pain reduction
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: 4 weeks
|
0 means no pain and 10 means worst pain ever
|
4 weeks
|
|
Range of motion
Time Frame: 4 weeks
|
Goniometer will be used to assess the ranges.
lower values means more limited ROM and more values means normal
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 10, 2023
Primary Completion (Actual)
May 9, 2023
Study Completion (Actual)
May 9, 2023
Study Registration Dates
First Submitted
May 13, 2023
First Submitted That Met QC Criteria
May 22, 2023
First Posted (Actual)
June 1, 2023
Study Record Updates
Last Update Posted (Actual)
June 1, 2023
Last Update Submitted That Met QC Criteria
May 22, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 342
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Have not decided yet
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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