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The comparative effect of dry needling versus ultrasound therapy in the treatment of active rhomboid trigger points.

Phase 1
Conditions
Musculoskeletal Diseases
Registration Number
PACTR202006473495513
Lead Sponsor
niversity of Johannesburg Health Science Chiroparctic Department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
All
Target Recruitment
30
Inclusion Criteria

Participants are either male or female aged between 18-50 years old –reason for a minimum age of 18 so that parental consent is avoided, and participants can sign their own consent forms, and the maximum age of 50 is to avoid degenerative changes that may be present.
Participants presenting with active rhomboid trigger point pain
Rhomboid Trigger point diagnosis according to the following criteria:
Presence of hyperirritable palpable nodule within a taut band of muscle.
Spot tenderness over the palpable nodule
With a pain referral along the vertebral border of scapula between the scapula and Paraspinal muscles. It may spread upwards to the spinous portion of the scapula and pain patterns resemble that of the levator scapulae muscle but without the neck component and without restriction to neck rotation.

Exclusion Criteria

Participants with any contraindication to ultrasound therapy obtained on case history and physical examination
Participants with any contraindications to dry needling obtained on case history and physical examination
Participants receiving any other form of treatment such as physiotherapy, other chiropractic treatment or any medication, such as muscle relaxants, analgesics or anti-inflammatories that will interfere with the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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