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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-25
SponsorFoundation University Islamabad

About this trial

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).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Amateur football players aged 18-25 years.

Disqualifiers

History of calf muscle tear, fracture, or lower limb surgery.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dry Needling

    Procedure/Surgery

    A single-session myofascial trigger point dry needling treatment will be administered to identified trigger points in the gastrocnemius and/or soleus muscles using sterile disposable filiform needles. The objective is to mechanically disrupt the dysfunctional motor end plate, elicit local twitch responses, reduce nociceptive activity, and restore muscle function. The intervention is delivered under aseptic conditions by a trained physiotherapist following standard safety guidelines. Post-procedure monitoring will be conducted for minor adverse effects such as soreness or bleeding.

  • Sham Needling

    Procedure/Surgery

    A simulated needling procedure designed to act as a placebo comparator will be applied without skin penetration. The technique reproduces the visual, tactile, and contextual components of dry needling to maintain participant blinding while avoiding physiological stimulation of the muscle. This allows isolation of the true therapeutic effect of dry needling from psychological or expectancy-related responses.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Group A - Dry Needling GroupExperimental treatment 1 intervention
Group B: Group B - Sham Needling GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain Pressure Threshold

Pressure Pain Threshold will be measured at the identified myofascial trigger point in the gastrocnemius or soleus using a handheld pressure algometer. The participant will indicate the point at which applied pressure first becomes painful. The recorded value (kg/cm²) reflects mechanical pain sensitivity of the trigger point.

Time frame
Baseline (Day 0, pre-intervention) and Immediately Post-intervention (within 15 minutes after intervention).
2

Functional Performance

Functional performance will be assessed using Single leg hop test ( distance in centimeters).The Single Leg Hop Test measures lower limb explosive power. Participants will perform three maximal forward hops on one leg. The distance (in centimeters) from the starting line to the heel landing point will be recorded. The average of three trials will be used for analysis. Greater distance indicates improved functional performance.

Time frame
Baseline (Day 0, pre-intervention) and Immediately Post-intervention (within 15 minutes after intervention).
3

Sprint Speed

Sprint speed will be accessed by Shuttle run test. The speed and agility of lower limb in calf muscle by time taken to complete a short distance shuttle sprint. It reflects the explosive function of calf muscle which is essential for acceleration and direction change in football. Sprint speed will be assessed using a 20-meter shuttle run test. Participants will run back and forth between two markers placed 20 meters apart as quickly as possible. Two trials will be performed, and the fastest time (in seconds) will be recorded to the nearest 0.1 second. Lower time indicates better sprint performance.

Time frame
Baseline (Day 0, pre-intervention) and Immediately Post-intervention (within 15 minutes after intervention).

Secondary outcomes

1

Range of Motion of Ankle Dorsiflexion

Ankle dorsiflexion will be measured in degrees using a universal goniometer. Three readings will be taken and averaged. Higher degrees indicate improved flexibility.

Time frame
Baseline (Day 0, pre-intervention) and Immediately Post-intervention (within 15 minutes after intervention).

Other outcomes

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