Effectiveness of Dry Needling Versus Manual Trigger Point Release on Active Rhomboid Trigger Points
1 other identifier
interventional
48
1 country
1
Brief Summary
This study compares dry needling and manual trigger point release for treating active rhomboid trigger points in 48 patients, assessing pain, ROM, and function. It addresses a gap in evidence for optimal pain management in upper back myofascial pain. Findings will guide clinical practice for more effective, evidence-based interventions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 23, 2025
CompletedFirst Submitted
Initial submission to the registry
July 3, 2025
CompletedFirst Posted
Study publicly available on registry
July 14, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedApril 8, 2026
April 1, 2026
3 months
July 3, 2025
April 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Numeric pain rating scale (NPRS)
A subjective pain assessment tool where patients rate their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain).
2 Weeks
Goniometer
The goniometer is a handheld device with a protractor and movable arms used to precisely measure joint range of motion in degrees.
2 Weeks
DASH Questionnaire
The DASH Questionnaire is a 30-item self-report tool assessing upper extremity function and symptoms in daily activities, scored from 0 (no disability) to 100 (severe disability).
2 Weeks
Study Arms (2)
dry needling trigger release therapy
EXPERIMENTALThis group will undergo dry needling trigger release therapy. Total of 2 sessions (one per week) followed by home based exercises plan. Treatment protocol of both groups will include Therapeutic ultrasound, Cold pack application and Home based exercise plan.
MANUAL TRIGGER POINT RELEASE
EXPERIMENTALManual trigger release will be given to the other group. Total of 2 sessions (one per week) followed by same home based exercises plan will be given to the both groups. Treatment protocol of both groups will include Therapeutic ultrasound, Cold pack application and Home based exercise plan.
Interventions
The dry needling intervention involved inserting sterile filiform needles directly into active rhomboid trigger points for 1-2 sessions (1 session/week) to elicit local twitch responses and relieve tension.
The manual trigger point release intervention involved applying sustained pressure to active rhomboid trigger points followed by passive stretching to release muscle tension and improve mobility.
Eligibility Criteria
You may qualify if:
- Presence of a clinically confirmed active trigger point in the rhomboid muscle based on established criteria (e.g., palpable tight band, local tenderness, referred pain pattern).
- Pain Level: Moderate to severe pain intensity (e.g., 4 or higher on a Visual Analog Scale or Numeric Pain Rating Scale).
- Duration of Symptoms: pain for at least 4 weeks.
You may not qualify if:
- Patient with conditions that may contribute to neck and subscapular pain other than rhomboid:
- fibromyalgia
- Rheumatic and inflammatory disease
- Recent Surgery
- Diabatic
- Cervical radiculopathy and nerve entrapment
- Pregnancy
- Malignancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Riphah International University, Malakand
Chakdara, KPK, 18800, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amna Anum, ms
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 3, 2025
First Posted
July 14, 2025
Study Start
April 23, 2025
Primary Completion
July 28, 2025
Study Completion
December 31, 2025
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share