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

16 сентября 2026 г. обновлено: 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).

Обзор исследования

Статус

Завершенный

Тип исследования

Интервенционный

Регистрация (Действительный)

49

Фаза

  • Непригодный

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Места учебы

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

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

  • Ребенок
  • Взрослый

Принимает здоровых добровольцев

Да

Описание

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

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

Как устроено исследование?

Детали дизайна

  • Основная цель: Другой
  • Распределение: Рандомизированный
  • Интервенционная модель: Параллельное назначение
  • Маскировка: Нет (открытая этикетка)

Оружие и интервенции

Группа участников / Армия
Вмешательство/лечение
Активный компаратор: 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.
Другие имена:
  • САЕ
Активный компаратор: 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.

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Changes in eccentric adduction strength after 8 week training period
Временное ограничение: 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.

Вторичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Changes in isometric adduction strength and abduction strength after 8 week training period
Временное ограничение: 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
Временное ограничение: 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.

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Спонсор

Следователи

  • Главный следователь: Apostolos Theos, PhD, Umeå University
  • Главный следователь: Kajsa Gilenstam, PhD, Umeå University

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Действительный)

17 января 2025 г.

Первичное завершение (Действительный)

1 июня 2026 г.

Завершение исследования (Действительный)

1 июня 2026 г.

Даты регистрации исследования

Первый отправленный

1 июня 2026 г.

Впервые представлено, что соответствует критериям контроля качества

16 сентября 2026 г.

Первый опубликованный (Действительный)

17 сентября 2026 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

17 сентября 2026 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

16 сентября 2026 г.

Последняя проверка

1 июня 2026 г.

Дополнительная информация

Термины, связанные с этим исследованием

Другие идентификационные номера исследования

  • Dnr 2024-07167-01

Планирование данных отдельных участников (IPD)

Планируете делиться данными об отдельных участниках (IPD)?

НЕТ

Описание плана IPD

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

Информация о лекарствах и устройствах, исследовательские документы

Изучает лекарственный продукт, регулируемый FDA США.

Нет

Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.

Нет

Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .

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