NCT07569484

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.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
12mo left

Started May 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress2%
May 2026Apr 2027

First Submitted

Initial submission to the registry

April 29, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

May 6, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2027

Last Updated

May 6, 2026

Status Verified

April 1, 2026

Enrollment Period

5 months

First QC Date

April 29, 2026

Last Update Submit

April 29, 2026

Conditions

Keywords

Dry NeedlingHamstring Strain

Outcome Measures

Primary Outcomes (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.

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

Secondary Outcomes (4)

  • 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

Study Arms (2)

Control Group (A)

ACTIVE COMPARATOR

Participants will receive only the standard rehabilitation program without dry needling.

Procedure: Standard Rehabilitation Program

Intervention Group (B)

EXPERIMENTAL

Participants will receive dry needling treatment in addition to a standard rehabilitation program for chronic hamstring strain

Procedure: Dry NeedlingProcedure: Standard Rehabilitation Program

Interventions

Dry NeedlingPROCEDURE

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.

Intervention Group (B)

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

Control Group (A)Intervention Group (B)

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Abu Qir General Hospital

Alexandria, Alexandria Governorate, Egypt

Location

Related Publications (15)

  • Petersen J, Thorborg K, et al. Eccentric training prevents hamstring injuries. Am J Sports Med. 2011;39(11):2296-2303.

    BACKGROUND
  • Espejo-Antúnez L, et al. Dry needling systematic review. Complement Ther Med. 2017;33:46-57. https://doi.org/10.1016/j.ctim.2017.06.004

    BACKGROUND
  • Ekstrand J, Hägglund M, Waldén M. Muscle injuries in professional football. Am J Sports Med. 2016;44(3):576-585. https://doi.org/10.1177/0363546515621377

    BACKGROUND
  • 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

    BACKGROUND
  • Croisier JL. Recurrent hamstring injury risk factors. Sports Med. 2004;34(10):681-695. https://doi.org/10.2165/00007256-200434100-00005

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

    BACKGROUND
  • 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

    BACKGROUND
  • 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

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

    BACKGROUND
  • Brukner P. Hamstring injuries: prevention and treatment update. Br J Sports Med. 2015;49(19):1241-1244. https://doi.org/10.1136/bjsports-2014-094427

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

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

    BACKGROUND
  • Bahr R, Thorborg K, Ekstrand J. Nordic hamstring survey and prevention adherence. Br J Sports Med. 2015;49(22):1466-1471. https://doi.org/10.1136/bjsports-2015-094826

    BACKGROUND
  • Askling CM, Tengvar M, Saartok T, Thorstensson A. Acute hamstring injuries in elite football: RCT comparing rehabilitation protocols. Br J Sports Med. 2013;47(15):953-959. https://doi.org/10.1136/bjsports-2013-092165

    BACKGROUND
  • Ahmad CS, Redler LH, Ciccotti MG, Maffulli N, Longo UG, Bradley J. Evaluation and management of hamstring injuries. Am J Sports Med. 2013;41(2):293-302. https://doi.org/10.1177/0363546512466064

    BACKGROUND

MeSH Terms

Interventions

Dry Needling

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy Modalities

Study Officials

  • Amr Anas, BSc

    Cairo University

    PRINCIPAL INVESTIGATOR
  • Ebtessam Gomaa, PhD

    Cairo University

    STUDY DIRECTOR
  • Marihan Makary

    Cairo University

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Master's Student, Faculty of Physical Therapy, Cairo University

Study Record Dates

First Submitted

April 29, 2026

First Posted

May 6, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

April 30, 2027

Last Updated

May 6, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations