Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

The Effectiveness of Two Different Interventions on Hip Adduction Strength in Junior Floorball Players

16 de setembro de 2026 atualizado por: Kajsa Gilenstam, Umeå University

The Effectiveness of Two Different Interventions on Hip Adduction Strength in Junior Floorball Players - A Randomized Controlled Trial

Study type The present study is a two- armed randomized controlled trial. Study setting and participants 50 floorball players in high-school level will be invited to participate. An a priori power calculation indicated that 40 participants are required to detect an effect size of 0,3, with a significance level of 0.05 and a statistical power of 80%.

Recruitment and study procedure The recruitment will be performed in two steps; (1) The project will be presented to responsible floorball coaches at one high-school with the aim to get consent to contact the players in their floorball group. (2) The Research Group will visit the players to ask for individual consent.

Baseline assessment Three assessments will be performed: (a) questionnaire including demographic data, injury history, history of adductor strength training and information dominant leg, history of lower limb and lower back problems and previous experience of groin specific strength training. (b) eccentric hip adductor strength measured with a handheld dynamometer (c) isometric hip adductor and abductor strength measured with the ForceFrame Strength System (VALD).

Randomization, stratification and statistical analysis Randomization will follow an individual-randomization procedure. Randomization will take place after completion of baseline strength measurements. Allocation followed a 1:1 ratio, where the two intervention groups are equal in size. All stratification follows the allocation described under "Randomization" above.

The following variables will be stratified: Sex, and eccentric hip adductor strength (measured with a handheld dynamometer) at baseline. Analyses will follow the intention-to-treat principle using mixed-effects models.

Intervention

The intervention will consist of two parallel groups:

  • Progressive training program using the Copenhagen Adductor Exercise (CAE).
  • Progressive training program using the Adductor Slide (AS). The interventions followed a progressive protocol. The exercise was incorporated into the participants' regular training and took approximately 10 minutes on the days the intervention was performed. The intervention protocol for both groups followed an 8-week progressive loading structure with gradual increases in training volume over time. During week 1, participants completed 2 sessions per week, performing 2 sets of 6 repetitions per side. In weeks 2 and 3, the number of repetitions was increased to 8 and 10 per side, respectively, while maintaining the same weekly frequency and number of sets. In week 4, the number of sets was increased from 2 to 3, while repetitions remained at 10 per side. During weeks 5 and 6, repetitions were further increased to 12 per side, followed by 15 repetitions per side during weeks 7 and 8. Overall, the protocol progressively increased training load by manipulating repetitions first, then sets, and finally maintaining a higher training volume in the final phase.

For both interventions, each repetition was performed with a 3-second eccentric phase and a 3-second concentric phase.

Implementation and adherence The intervention was supervised by the research group. Attendance was recorded at each intervention session.

Follow-up assessment Three assessments were performed: (a) questionnaire assessing how the players experienced the intervention, if any adverse events occured, their motivation to perform the intervention and if they experienced DOMS (delayed onset muscle soreness) during the intervention (b) eccentric hip adductor strength measured with a handheld dynamometer (c) isometric hip adductor and abductor strength measured with the ForceFrame Strength System (VALD).

Outcome variables and analyses. Between-group effects will be calculated. Main outcome variables will be;

  • Eccentric hip adductor strength (measured with handheld dynamometer). The unit used will be Nm/kg.
  • Isometric hip adductor and abductor strength (measured with the ForceFrame Strength System, VALD). The unit used will be Nm/kg.
  • Ratio between isometric hip adductor and isometric hip abductor strength (measured with the ForceFrame Strength System, VALD). Percentage (i.e a measure of the strength balance between the hip adductors and abductors. Lower values indicate relatively weaker adductors compared with abductors) will be calculated to express this ratio. Potential confounders that will be analyzed as interactions will include;
  • Attendance to the intervention
  • Motivation to perform the intervention
  • Experienced DOMS
  • Contamination (i.e if the participant performed hip adductor specific training outside the intervention).

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

49

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Västerbotten County
      • Umeå, Västerbotten County, Suécia, 90187
        • Umeå Energi Arena

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

  • Filho
  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Floorball players between 16-20 years old
  • Not actively using any of the interventions in their daily training

Exclusion Criteria:

  • Pain or injury to the lower extremities or lower back that hinders the person from performing the assigned intervention

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: Outro
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Copenhagen Adductor Exercise
The Copenhagen Adduction exercise protocol followed an 8-week progressive loading structure with gradual increases in training volume over time. During week 1, participants completed 2 sessions per week, performing 2 sets of 6 repetitions per side. In weeks 2 and 3, the number of repetitions was increased to 8 and 10 per side, respectively, while maintaining the same weekly frequency and number of sets. In week 4, the number of sets was increased from 2 to 3, while repetitions remained at 10 per side. During weeks 5 and 6, repetitions were further increased to 12 per side, followed by 15 repetitions per side during weeks 7 and 8. Overall, the protocol progressively increased training load by manipulating repetitions first, then sets, and finally maintaining a higher training volume in the final phase. Each repetition is performed with a 3-second eccentric phase and a 3-second concentric phase.
The Copenhagen Adductor Exercise is performed with a partner and primarily targets the hip adductor muscles. The athlete begins in a side plank position with the lower forearm placed directly under the shoulder and the body held in a straight line. A partner stands beside the athlete and supports the upper leg by holding the ankle and, if needed, the knee. The lower leg remains free beneath the body. From the starting position, the athlete lifts the body upward by pressing the supported upper leg down into the partner's hands while simultaneously raising the lower leg to meet the upper leg. The body should remain straight and stable throughout the movement, with the hips kept elevated and aligned. The athlete then slowly lowers the lower leg back to the starting position in a controlled manner while maintaining trunk stability. After completing the prescribed repetitions on one side, the exercise is repeated on the opposite side.
Outros nomes:
  • CAE
Comparador Ativo: Adductor Slide
The Adductor Slide exercise protocol followed an 8-week progressive loading structure with gradual increases in training volume over time. During week 1, participants completed 2 sessions per week, performing 2 sets of 6 repetitions per side. In weeks 2 and 3, the number of repetitions was increased to 8 and 10 per side, respectively, while maintaining the same weekly frequency and number of sets. In week 4, the number of sets was increased from 2 to 3, while repetitions remained at 10 per side. During weeks 5 and 6, repetitions were further increased to 12 per side, followed by 15 repetitions per side during weeks 7 and 8. Overall, the protocol progressively increased training load by manipulating repetitions first, then sets, and finally maintaining a higher training volume in the final phase.
The Adductor Slide is performed in standing and targets the hip adductors while also challenging balance and trunk control. The athlete stands with one foot on a sliding surface and the other firmly planted on the floor. A resistance band is placed around the ankle of the sliding leg and positioned to pull the leg laterally away from the body. The athlete slowly slides the leg out to the side while bending the stance leg into a controlled side-lunge position, keeping the trunk upright and pelvis stable. The sliding leg is then actively pulled back to the starting position against the resistance of the band using the hip adductor muscles. The movement should be slow and controlled. After completing the prescribed repetitions, the exercise is repeated on the opposite side. Each repetition is performed with a 3-second eccentric phase and a 3-second concentric phase.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Changes in eccentric adduction strength after 8 week training period
Prazo: Measured at baseline (pre intervention) and directly after the intervention (post intervention). Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.
Eccentric adduction strength measured with a handheld dynamometer
Measured at baseline (pre intervention) and directly after the intervention (post intervention). Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Changes in isometric adduction strength and abduction strength after 8 week training period
Prazo: Pre and post intervention. Pre Intervention = Maximum 14 days before the intervention starts. Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.
Isometric adductor strength and abductor strength measured with a stationary strength testing system (VALD ForceFrame)
Pre and post intervention. Pre Intervention = Maximum 14 days before the intervention starts. Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.
Changes in ratio between isometric adduction strength and abduction strength after 8 week training period
Prazo: Measured at baseline (pre intervention) and directly after the intervention (post intervention). Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.
Ratio between isometric adduction strength and abduction strength measured with a stationary strength testing system (VALD ForceFrame)
Measured at baseline (pre intervention) and directly after the intervention (post intervention). Post intervention = Intervention ends on a Friday, post-intervention testing will be performed during the upcoming 14 days.

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Apostolos Theos, PhD, Umeå University
  • Investigador principal: Kajsa Gilenstam, PhD, Umeå University

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 (Real)

17 de janeiro de 2025

Conclusão Primária (Real)

1 de junho de 2026

Conclusão do estudo (Real)

1 de junho de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

1 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de setembro de 2026

Primeira postagem (Real)

17 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

17 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

16 de setembro de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • Dnr 2024-07167-01

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

All researchers that will be working with this data are stated in this registration

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

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever