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Clinical Trials/CTRI/2025/07/090499
CTRI/2025/07/090499
Not yet recruiting
Not Applicable

Effectiveness Of Dry Needling Vs. Ultrasound Therapy on Pain and Strength Associated with Rhomboid Muscle Trigger Points in College-Going Students: A 4-week Single-Blinded Randomized Controlled Trial

DVVPFs College of Physiotherapy, Ahmadnagar1 site in 1 country38 target enrollmentStarted: August 20, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
DVVPFs College of Physiotherapy, Ahmadnagar
Enrollment
38
Locations
1
Primary Endpoint
pain, pain pressure threshold and strength

Overview

Brief Summary

This study aims to find out the effectiveness of dry needling vs ultrasound therapy on pain and strength associated with the rhomboid muscle trigger points in college-going students. RCT. 38 subjects, 19 in each group, will be recruited based on inclusion and exclusion criteria. There will be 2 groups dry needling group and ultrasound therapy group, Conventional treatment will be given to all groups. Outcome measures are pain, ,pain pressure threshold and strength. Pre-intervention outcome measures will be taken. Intervention will be given for 4 weeks, and post-treatment outcome measures will be taken. follow-up will be taken after 4 weeks. The analysis and result will be calculated.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 26.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Presence of Rhomboid Muscle Trigger Points: Confirmed by palpation.
  • 2.Participants experiencing chronic or recurrent upper back pain associated with trigger points for at least 4 weeks.
  • Participants should not have received dry needling, physiotherapy, or other musculoskeletal treatments targeting the muscles in the past 4 weeks.

Exclusion Criteria

  • 1.Recent Injury or Surgery: History of trauma, fractures, or surgery in the upper back, neck, or shoulder region within the past 6 months.
  • 2.Skin infections or open wounds at the treatment site.
  • Bleeding disorders (e.g., haemophilia) or anticoagulant therapy.
  • 4.Fear of needles (trypanophobia).
  • 5.Regular Use of Pain Medication: Participants taking opioids, muscle relaxants, or corticosteroids that could influence pain perception.
  • Engagement in Conflicting Treatments.

Outcomes

Primary Outcomes

pain, pain pressure threshold and strength

Time Frame: At baseline

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
DVVPFs College of Physiotherapy, Ahmadnagar
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Vibhuti Manoj Patil

DVVPFs College of Physiotherapy, Ahilyanagar

Study Sites (1)

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