Back to resultsIntegrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction
Primary Purpose
Myofascial Trigger Point Pain
Status
Enrolling by invitation
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Integrated Neuromuscular Inhibition Technique
Myofascial Release
Sponsored by
About this trial
This is an interventional health services research trial for Myofascial Trigger Point Pain
Eligibility Criteria
Inclusion Criteria: ● Age between 25-40 Both males and females included Participants suffering from recent cervical pain without any pathology. Exclusion Criteria: ● Participants having cervical radiculopathy Having recent trauma of the cervical spine Non-cooperative subject
Sites / Locations
- Chaudhary Muhammad Akram Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Neuromuscular Inhibition Technique
Myofascial Release
Arm Description
Outcomes
Primary Outcome Measures
Cervical Range of Motion measurement
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05816161
Brief Title
Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction
Official Title
Comparison of The Effects of The Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction in Individuals With Nonspecific Cervical Pain
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Superior University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
to findout the improvement by Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myofascial Trigger Point Pain
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Neuromuscular Inhibition Technique
Arm Type
Experimental
Arm Title
Myofascial Release
Arm Type
Other
Intervention Type
Diagnostic Test
Intervention Name(s)
Integrated Neuromuscular Inhibition Technique
Intervention Description
Exercises
Intervention Type
Diagnostic Test
Intervention Name(s)
Myofascial Release
Intervention Description
Exercises
Primary Outcome Measure Information:
Title
Cervical Range of Motion measurement
Time Frame
6 Months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
● Age between 25-40
Both males and females included
Participants suffering from recent cervical pain without any pathology.
Exclusion Criteria:
● Participants having cervical radiculopathy
Having recent trauma of the cervical spine
Non-cooperative subject
Facility Information:
Facility Name
Chaudhary Muhammad Akram Hospital
City
Lahore
State/Province
Punjab
Country
Pakistan
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction
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