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Clinical Trials/NCT05816161
NCT05816161Enrolling By InvitationNot Applicable

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

Superior University1 site in 1 country30 target enrollmentStarted: April 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
30
Locations
1
Primary Endpoint
Cervical Range of Motion measurement

Study Overview

Brief Summary

to findout the improvement by Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
25 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Neuromuscular Inhibition Technique

Experimental

Intervention: Integrated Neuromuscular Inhibition Technique (Diagnostic Test)

Myofascial Release

Other

Intervention: Myofascial Release (Diagnostic Test)

Outcomes

Primary Outcomes

Cervical Range of Motion measurement

Time Frame: 6 Months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Study Sites (1)

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