Actively Recruiting

Phase Not Applicable
Age: 18Years - 25Years
All Genders
NCT07525921

Immediate Effect of Dry Needling on Calf Muscles Pain Pressure Threshold,Sprint Speed and Functional Performance in Amateur Football Player

Led by Foundation University Islamabad · Updated on 2026-04-13

60

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomised single-blind trial will evaluate the immediate effect of a single session of dry needling versus sham needling on calf muscle myofascial trigger points among amateur football players aged 18-25 years. Primary and secondary outcomes are Pressure Pain Threshold (algometer), Sprint Speed (shuttle run test), and Functional Performance (single-leg hop). Outcomes will be measured immediately pre- and post-intervention. Data analysis will be performed in SPSS version 27 using paired and independent t-tests (p \< 0.05).

CONDITIONS

Official Title

Immediate Effect of Dry Needling on Calf Muscles Pain Pressure Threshold,Sprint Speed and Functional Performance in Amateur Football Player

Who Can Participate

Age: 18Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Amateur football players aged 18 to 25 years
  • Participation in club-level football for at least one year
  • Presence of active myofascial trigger point in gastrocnemius or soleus confirmed by palpation
  • Willingness to participate and provide informed consent
Not Eligible

You will not qualify if you...

  • History of calf muscle tear, fracture, or lower limb surgery
  • Current use of muscle relaxants or anti-inflammatory medication
  • Known bleeding disorders or anticoagulant therapy
  • Local infection, skin lesion, or contraindication to dry needling
  • Neurological or vascular disorders affecting lower limb function

AI-Screening

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Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Islamabad, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

H

Hamza Aliyan, DPT

CONTACT

M

Marwa Asim, MS-OMPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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