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Effectiveness of Dry Needling in Athletes With Chronic Hamstring Strain

29 de abril de 2026 atualizado por: Amr Mostafa Kamal Anas, Cairo University

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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Estimado)

38

Estágio

  • Não aplicável

Contactos e Locais

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Contato de estudo

Locais de estudo

    • Alexandria Governorate
      • Alexandria, Alexandria Governorate, Egito
        • Abu Qir General Hospital
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

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).

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Control Group (A)
Participants will receive only the standard rehabilitation program without dry needling.
Participants will receive a standardized rehabilitation program including stretching and eccentric strengthening exercises for hamstring muscles without dry needling.
Experimental: Intervention Group (B)
Participants will receive dry needling treatment in addition to a standard rehabilitation program for chronic hamstring strain
Participants will receive a standardized rehabilitation program including stretching and eccentric strengthening exercises for hamstring muscles without dry needling.
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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Pain Intensity
Prazo: 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.
Baseline (pre-intervention) and after 6 weeks of treatment

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Functional Performance
Prazo: Baseline (pre-intervention) and after 6 weeks of treatment
Functional outcomes will be assessed using the Lower Extremity Functional Scale (LEFS) to evaluate the impact of intervention on daily and sports-related activities.
Baseline (pre-intervention) and after 6 weeks of treatment
Hamstring Muscle Strength
Prazo: Baseline (pre-intervention) and after 6 weeks of treatment
Hamstring muscle strength will be measured using a handheld dynamometer during maximal isometric contraction.
Baseline (pre-intervention) and after 6 weeks of treatment
Hamstring Flexibility
Prazo: Baseline (pre-intervention) and after 6 weeks of treatment
Hamstring flexibility will be assessed using the popliteal angle test with a universal goniometer.
Baseline (pre-intervention) and after 6 weeks of treatment
Kicking Speed
Prazo: Baseline (pre-intervention) and after 6 weeks of treatment
Kicking speed will be measured using a radar gun to assess football-specific performance.
Baseline (pre-intervention) and after 6 weeks of treatment

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Amr Anas, BSc, Cairo university
  • Diretor de estudo: Ebtessam Gomaa, PhD, Cairo university
  • Diretor de estudo: Marihan Makary, Cairo university

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

  • Petersen J, Thorborg K, et al. Eccentric training prevents hamstring injuries. Am J Sports Med. 2011;39(11):2296-2303.
  • 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
  • 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
  • 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. Recurrent hamstring injury risk factors. Sports Med. 2004;34(10):681-695. https://doi.org/10.2165/00007256-200434100-00005
  • 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 update. Br J Sports Med. 2015;49(19):1241-1244. https://doi.org/10.1136/bjsports-2014-094427
  • 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. Nordic hamstring survey and prevention adherence. Br J Sports Med. 2015;49(22):1466-1471. https://doi.org/10.1136/bjsports-2015-094826
  • 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
  • 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

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de maio de 2026

Conclusão Primária (Estimado)

30 de setembro de 2026

Conclusão do estudo (Estimado)

30 de abril de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

29 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

29 de abril de 2026

Primeira postagem (Real)

6 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

29 de abril de 2026

Última verificação

1 de abril de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • P.T.REC/012/006296

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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Ensaios clínicos em Distensão Muscular dos Isquiotibiais

Ensaios clínicos em Standard Rehabilitation Program

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