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Clinical Trials/CTRI/2025/08/093825
CTRI/2025/08/093825Not yet recruitingNot Applicable

Comparison between dry needling and ischemic compression therapy in non-specific fascio- thoracic pain among young adults.

Diksha Solanki1 site in 1 country80 target enrollmentStarted: September 15, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
Pain

Study Overview

Brief Summary

The research proposal titled “Comparison between Dry Needling and Ischemic Compression Therapy in Non-Specific Fascio-Thoracic Pain among Young Adults” by focuses on evaluating and comparing the effectiveness of two physiotherapy interventions for managing thoracic fascia-related pain. Non-specific fascio-thoracic pain, often associated with myofascial trigger points, poor posture, and muscular imbalances, is a common clinical problem in young adults. The study aims to assess the impact of dry needling and ischemic compression therapy on pain reduction, pressure pain threshold, and trigger point release. Conducted as an experimental study with 80 participants aged 18–40 years, it will involve dividing subjects into two groups: one receiving dry needling at specific thoracic paraspinal levels and the other undergoing ischemic compression at active trigger points. Pain will be measured using the Numeric Pain Rating Scale, and pressure pain threshold will be assessed with an algometer. By directly comparing these two interventions, the study seeks to determine which technique provides greater effectiveness in alleviating fascio-thoracic pain and improving functional outcomes.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 40.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Subjects with non-specific fascio- thoracic pain.
  • Both male and female subjects aged between 18- 40 years
  • History of thoracic pain
  • Subjects with a hypersensitive nodule within a palpable taut band of skeletal muscle.

Exclusion Criteria

  • Subjects on anti-coagulant or anti-aggregate medications
  • History of systemic or local infection
  • History of heart surgery in past 6 months
  • History thoracic rib and thoracic spine fracture
  • Subjects suffering from malignancy
  • Subjects having fear of needles.

Outcomes

Primary Outcomes

Pain

Time Frame: 2 weeks

Height

Time Frame: 2 weeks

Weight

Time Frame: 2 weeks

Pressure pain threshold

Time Frame: 2 weeks

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Diksha Solanki
Sponsor Class
Other [myself]
Responsible Party
Principal Investigator
Principal Investigator

Diksha Solanki

Guru Nanak Dev University

Study Sites (1)

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