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临床试验/NCT07822568
NCT07822568已完成不适用

Comparison of Hip Adductor Training Using an Isokinetic Device Versus the Copenhagen Adduction Exercise: A Randomized Controlled Trial

University of Primorska1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2024年9月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
55
试验地点
1
主要终点
Eccentric adductor peak torque

研究概览

简要总结

This randomized controlled trial compared two exercise approaches for strengthening the hip adductor muscles in healthy, recreationally active adults. Participants were assigned to one of three groups: training using a custom isokinetic device, training using the Copenhagen adduction exercise, or a control group that did not perform the specific hip adductor training. The intervention lasted 8 weeks. The device-based program used controlled eccentric muscle actions, in which the hip adductors produce force while being lengthened, whereas the Copenhagen adduction exercise involved a commonly used body-weight strengthening exercise.

The purpose of the study was to determine how these two types of hip adductor training affect muscle strength and other physical characteristics that may be relevant to performance and the prevention of groin and hip adductor injuries. The main research question was whether training with the isokinetic device produces different and potentially greater adaptations than the Copenhagen adduction exercise and no specific training. The study hypothesis was that device-based eccentric training would lead to greater improvements in hip adductor strength and related functional and muscle characteristics than copenhagen adduction exercise training, while the control group would show little or no change.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy and free from musculoskeletal injury at the time of enrollment;
  • Recreationally active males;
  • Able to successfully complete 5 repetitions of the Copenhagen adduction exercise.

排除标准

  • Serious injury to nervous, muscular, skeletal, or connective tissue involving the back, hip, or lower extremities within the previous 12 months
  • Inability to perform the Copenhagen adduction exercise

研究组 & 干预措施

Isokinetic device-based training

Experimental

Participants completed an 8-week hip adductor training program using an isokinetic device. Training consisted of controlled eccentric hip adduction exercise, in which the hip adductor muscles produced force while being lengthened. Training was performed twice per week with progressive training volume.

干预措施: Isokinetic device-based hip adductor training (Other)

Copenhagen adduction exercise training

Experimental

Participants completed an 8-week hip adductor strengthening program using the Copenhagen adduction exercise. Training was performed twice per week, with the number of sets and repetitions progressively increased during the intervention.

干预措施: Copenhagen adduction exercise training (Other)

Control

No Intervention

Participants did not perform either of the study-specific hip adductor training programs during the 8-week intervention period.

结局指标

主要结局

Eccentric adductor peak torque

时间窗: Baseline and after the 8-week intervention

Eccentric hip adductor peak torque of the dominant leg measured using an isokinetic dynamometer (Humac Norm) at an angular velocity of 30°/s

Eccentric work

时间窗: Baseline and after the 8-week intervention

Work during eccentric hip adductor contraction of the dominant leg measured using an isokinetic dynamometer (Humac Norm) at an angular velocity of 30°/s

Adductor longus muscle thickness

时间窗: Baseline and after the 8-week intervention

Adductor longus muscle thickness measured using ultrasound imaging.

次要结局

  • Angle at peak torque during eccentric contraction(Baseline and after the 8-week intervention)
  • Concentric adductor peak torque(Baseline and after the 8-week intervention)
  • Concentric abductor peak torque(Baseline and after the 8-week intervention)
  • Hip Adduction:abduction strength ratio(Baseline and after the 8-week intervention)
  • Lateral shuffle test(Baseline and after the 8-week intervention)
  • Passive hip abduction range of motion(Baseline and after the 8-week intervention)
  • Adductor longus muscle stiffness(Baseline and after the 8-week intervention)
  • Passive resistance to hip abduction(Baseline and after the 8-week intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nejc Sarabon

Porf. Dr.

University of Primorska

研究点 (1)

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