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Clinical Trials/NCT05873010
NCT05873010RecruitingNot Applicable

Effectiveness Of Manual Compression and Stretching for The Myofascial Trigger Points in Upper Trapezius and Levator Scapulae

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

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
VAS (visual analogue scale) for pain
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

To compare the effectiveness of manual compression and stretching for myofascial trigger points in upper trapezius and levator scapulae in male office workers

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
25 Years to 45 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •male office workers with age of 25-45 working from Monday to Friday for 6-8 hours in a day.

Exclusion Criteria

  • •male office workers having any past trauma, chronic illness, any recent surgery and systemic diseases.

Outcomes

Primary Outcomes

VAS (visual analogue scale) for pain

Time Frame: 6 Months

Stretching for The Myofascial Trigger Points in Upper Trapezius and Levator Scapulae using VAS

mechanical algometer Scale for pain

Time Frame: 6 Months

Stretching for The Myofascial Trigger Points in Upper Trapezius and Levator Scapulae using mechanical algometer

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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