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Hamstring Muscle StrainNCT07569484

Effectiveness of Dry Needling in Athletes With Chronic Hamstring Strain

A study testing Dry Needling and Standard Rehabilitation Program in people with Hamstring Muscle Strain, run by Cairo University at 1 site in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 35 years, men only
Conditions the study is for
Hamstring Muscle Strain
What is being tested?
Dry Needling and Standard Rehabilitation Program
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
38 participants
Where
1 siteEgypt
Study dates
1 May 2026to 30 Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • Men only
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Egypt1 site
  • Abu Qir General Hospital

    Alexandria, Alexandria Governorate

    Amr Anas, BSc, +201023924004, amr.anas109@gmail.com

Other trials in Egypt

About this study

Official title: Effectiveness of Dry Needling on Athletes With Chronic Hamstring Strain

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.

Read the 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.

The results of this study are expected to provide evidence regarding the added value of dry needling in improving rehabilitation outcomes for athletes with chronic hamstring strain.

Being tested
Dry Needling, Standard Rehabilitation Program
Keywords
Dry Needling, Hamstring Strain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dry NeedlingProcedure or surgery

    Participants will receive dry needling treatment applied to active myofascial trigger points in the hamstring muscles (biceps femoris, semitendinosus, and semimembranosus). Sterile filiform needles will be inserted into identified trigger points to elicit local twitch responses and reduce muscle pain and tightness. Treatment will be performed in addition to a standardized rehabilitation program including stretching and strengthening exercises for the hamstring muscle group. Sessions will be administered over the study period according to a predefined treatment schedule.

  • Standard Rehabilitation ProgramProcedure or surgery

    Participants will receive a standardized rehabilitation program including stretching and eccentric strengthening exercises for hamstring muscles without dry needling.

Study groups in NCT07569484
Study groupRoleWhat they receive
Control Group (A)Active comparatorParticipants will receive only the standard rehabilitation program without dry needling.
Receives: Procedure: Standard Rehabilitation Program
Intervention Group (B)ExperimentalParticipants will receive dry needling treatment in addition to a standard rehabilitation program for chronic hamstring strain
Receives: Procedure: Dry Needling; Procedure: Standard Rehabilitation Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain Intensity

    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.

    Measured: Baseline (pre-intervention) and after 6 weeks of treatment

Secondary outcomes (4)
  1. Functional Performance

    Functional outcomes will be assessed using the Lower Extremity Functional Scale (LEFS) to evaluate the impact of intervention on daily and sports-related activities.

    Measured: Baseline (pre-intervention) and after 6 weeks of treatment

  2. Hamstring Muscle Strength

    Hamstring muscle strength will be measured using a handheld dynamometer during maximal isometric contraction.

    Measured: Baseline (pre-intervention) and after 6 weeks of treatment

  3. Hamstring Flexibility

    Hamstring flexibility will be assessed using the popliteal angle test with a universal goniometer.

    Measured: Baseline (pre-intervention) and after 6 weeks of treatment

  4. Kicking Speed

    Kicking speed will be measured using a radar gun to assess football-specific performance.

    Measured: Baseline (pre-intervention) and after 6 weeks of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion30 Sep 2026 (estimated)
  4. Study completion30 Apr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a randomized, parallel-group interventional study. Participants will be allocated into two groups: an experimental group receiving dry needling combined with conventional physiotherapy, and a control group receiving conventional physiotherapy alone.
Masking
None (open label)
Enrolment
38 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07569484
Sponsor's protocol ID
P.T.REC/012/006296
Status last verified
Apr 2026
First submitted
29 Apr 2026
Last updated
6 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Petersen J, Thorborg K, Nielsen MB, Budtz-Jorgensen E, Holmich P. Preventive effect of eccentric training on acute hamstring injuries in men's soccer: a cluster-randomized controlled trial. Am J Sports Med. 2011 Nov;39(11):2296-303. doi: 10.1177/0363546511419277. Epub 2011 Aug 8.

    PubMed 21825112
  • Espejo-Antunez L, Tejeda JF, Albornoz-Cabello M, Rodriguez-Mansilla J, de la Cruz-Torres B, Ribeiro F, Silva AG. Dry needling in the management of myofascial trigger points: A systematic review of randomized controlled trials. Complement Ther Med. 2017 Aug;33:46-57. doi: 10.1016/j.ctim.2017.06.003. Epub 2017 Jun 15.

    PubMed 28735825
  • Ekstrand J, Hagglund M, Walden M. Epidemiology of muscle injuries in professional football (soccer). Am J Sports Med. 2011 Jun;39(6):1226-32. doi: 10.1177/0363546510395879. Epub 2011 Feb 18.

    PubMed 21335353
  • Dunning J, et al. Dry needling clinical practice review. Phys Ther Rev. 2021;26(5-6):287-307. https://doi.org/10.1080/10833196.2021.1983244

  • Croisier JL. Factors associated with recurrent hamstring injuries. Sports Med. 2004;34(10):681-95. doi: 10.2165/00007256-200434100-00005.

    PubMed 15335244
  • Chaabene H, et al. Hamstring strength assessment systematic review. Sports Med Open. 2019;5:23. https://doi.org/10.1186/s40798-019-0198-7

  • Chamorro C, et al. Reliability of handheld dynamometry and isokinetic testing. Open Med. 2014;9(4):382-397. https://doi.org/10.1515/med-2014-0058

  • Canosa-Carro L, et al. Dry needling effects on hamstring flexibility and performance. J Sport Rehabil. 2022;31(3):254-261. https://doi.org/10.1123/jsr.2020-0225

  • Buckthorpe M, et al. Hamstring injuries in football: risk factors and RTP. Br J Sports Med. 2020;54(19):1081-1091.

  • Brukner P. Hamstring injuries: prevention and treatment-an update. Br J Sports Med. 2015 Oct;49(19):1241-4. doi: 10.1136/bjsports-2014-094427. Epub 2015 Jun 23.

    PubMed 26105015
  • Bourne MN, et al. Eccentric training and hamstring injury risk. Scand J Med Sci Sports. 2017;27(11):1180-1187.

  • Bahr R, et al. Hamstring injury prevention programs: systematic review. Br J Sports Med. 2018;52(17):1077-1085.

  • Bahr R, Thorborg K, Ekstrand J. Evidence-based hamstring injury prevention is not adopted by the majority of Champions League or Norwegian Premier League football teams: the Nordic Hamstring survey. Br J Sports Med. 2015 Nov;49(22):1466-71. doi: 10.1136/bjsports-2015-094826. Epub 2015 May 20.

    PubMed 25995308
  • Askling CM, Tengvar M, Thorstensson A. Acute hamstring injuries in Swedish elite football: a prospective randomised controlled clinical trial comparing two rehabilitation protocols. Br J Sports Med. 2013 Oct;47(15):953-9. doi: 10.1136/bjsports-2013-092165. Epub 2013 Mar 27.

    PubMed 23536466
  • Ahmad CS, Redler LH, Ciccotti MG, Maffulli N, Longo UG, Bradley J. Evaluation and management of hamstring injuries. Am J Sports Med. 2013 Dec;41(12):2933-47. doi: 10.1177/0363546513487063. Epub 2013 May 23.

    PubMed 23703914

Questions about this trial

What is this clinical trial studying?

A study testing Dry Needling and Standard Rehabilitation Program in people with Hamstring Muscle Strain, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amr Anas, BSc (+201023924004, amr.anas109@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain Intensity (time frame: Baseline (pre-intervention) and after 6 weeks of treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07569484, which also lists 15 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2026.

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