Effectiveness of Dry Needling on Athletes With Chronic Hamstring Strain
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Cairo University
- Enrollment
- 38
- Locations
- 1
- Primary Endpoint
- Pain Intensity
Study Overview
Brief Summary
This study aims to evaluate the effectiveness of dry needling in reducing pain and improving functional outcomes in athletes with chronic hamstring strain. Chronic hamstring injuries are common among athletes and often lead to persistent pain, reduced performance, and limitations in daily and sports activities.
Dry needling is a therapeutic technique used to target myofascial trigger points and relieve muscle tension. This study will compare the effects of dry needling with conventional physiotherapy interventions to determine its role in managing chronic hamstring strain.
Participants will be athletes diagnosed with chronic hamstring strain. Outcomes will include pain intensity, muscle flexibility, and functional performance. The results of this study may help improve rehabilitation strategies and provide evidence for the use of dry needling in sports injuries.
Detailed Description
Chronic hamstring strain (CHS) is a common musculoskeletal condition among athletes, particularly in sports involving high-speed running and sudden changes in direction. It is characterized by persistent or recurrent symptoms lasting more than three months and is often associated with reduced muscle flexibility, decreased performance, and an increased risk of reinjury.
Dry needling (DN) has emerged as a therapeutic intervention targeting myofascial trigger points to reduce pain, improve muscle function, and restore neuromuscular control. It is believed to act through both mechanical and neurophysiological mechanisms, including reduction of muscle tension and modulation of pain pathways.
This study aims to investigate the effectiveness of dry needling as an adjunct to conventional physiotherapy in athletes with chronic hamstring strain. Participants will be randomly assigned into two groups. The experimental group will receive dry needling combined with a structured physiotherapy program, while the control group will receive the same physiotherapy program without dry needling.
The physiotherapy program will include stretching exercises, strengthening exercises with an emphasis on eccentric loading, and functional training. Dry needling will be applied to identified trigger points in the hamstring muscles using standard clinical techniques.
Outcome measures will include pain intensity, hamstring flexibility, and functional performance. Assessments will be conducted before and after the intervention period.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 35 Years (Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male football players aged 18 to 35 years.
- •Diagnosed with chronic hamstring strain (CHS) confirmed by ultrasonography.
- •Injury duration of more than 3 months.
- •Classified as Grade I or Grade II hamstring strain.
- •Currently participating in the competitive phase of football.
- •Body Mass Index (BMI) between 21-25 kg/m².
Exclusion Criteria
- •Previous exposure to dry needling therapy.
- •Presence of any other current lower limb injuries.
- •Participation in another hamstring rehabilitation program.
- •Active skin infection at or near the treatment area.
- •Bleeding disorders or use of anticoagulant medications.
- •Severe needle phobia or psychological intolerance to needling.
- •Presence of neuromuscular disorders (e.g., muscular dystrophy or peripheral neuropathy).
Arms & Interventions
Control Group (A)
Participants will receive only the standard rehabilitation program without dry needling.
Intervention: Standard Rehabilitation Program (Procedure)
Intervention Group (B)
Participants will receive dry needling treatment in addition to a standard rehabilitation program for chronic hamstring strain
Intervention: Dry Needling (Procedure)
Intervention Group (B)
Participants will receive dry needling treatment in addition to a standard rehabilitation program for chronic hamstring strain
Intervention: Standard Rehabilitation Program (Procedure)
Outcomes
Primary Outcomes
Pain Intensity
Time Frame: Baseline (pre-intervention) and after 6 weeks of treatment
Pain intensity in chronic hamstring strain will be assessed using the Visual Analog Scale (VAS), a 10-cm scale ranging from 0 (no pain) to 10 (worst imaginable pain). Measurements will be taken at baseline and after completion of the intervention period to evaluate changes in pain perception.
Secondary Outcomes
- Functional Performance(Baseline (pre-intervention) and after 6 weeks of treatment)
- Hamstring Muscle Strength(Baseline (pre-intervention) and after 6 weeks of treatment)
- Hamstring Flexibility(Baseline (pre-intervention) and after 6 weeks of treatment)
- Kicking Speed(Baseline (pre-intervention) and after 6 weeks of treatment)
Investigators
Amr Mostafa Kamal Anas
Master's Student, Faculty of Physical Therapy, Cairo University
Cairo University