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临床试验/NCT07750327
NCT07750327Enrolling By Invitation不适用

A Pain-guided Rehabilitation Program in a Recreational Long-distance Runner With Long-standing Groin Pain: A Single-case Experimental Study

University of West Attica1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2026年7月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1
试验地点
1
主要终点
Return to sport time

研究概览

简要总结

Groin injuries are among the most common injuries in sports that require changes of directions, shooting, passing etc, and are presented both as acute and long-standing. Although there are many exercise-based rehabilitation programs for long-standing groin pain in athletes, there is still the need for a more flexible pain-guided program based on specific progression and return to sport criteria. In addition, there is no much focus on less demanding sports such as track and field. The current study introduces a pain-guided rehabilitation program for a long-distance runner with long-standing groin pain.

详细描述

A 38-year-old male recreational runner reported pain in his right groin (adductor and lower abdomen area). The mean pain level reported was 2 in a numeric pain rating scale (NPRS) of 0-10, which occasionally increased to 3. Aggravating exercises included straight abdominal sit-ups, sliding hip exercise, and hip adductor squeeze at 45 degrees. In addition, symptoms were provoked by laughing and sexual intercourse. The initial onset of pain was nine years before the athlete contacted the research team seeking assistance (2017). Pain was resolved after two years (2019) of systematic resistance training, but reappeared five years later. The athlete did not report any specific mechanism of the initial injury, but described an insidious pain presented during an intense running period. Although the athlete had a number of physiotherapy sessions within the last year, including electrotherapeutic modalities (TENS, radiofrequency therapy) and massage, there was no improvement of the pain in the groin area. His weekly training schedule during the month before the clinical examination included one running session (10 km), one upper limb resistance training session, and one groin-specific resistance training session. The athlete reported no previous musculoskeletal injuries, while no radiological examination had been performed.

The program will comprise two distinct phases. Phase A will consist of a baseline monitoring period, during which the athlete will exclusively perform adductor strength testing without any exercise intervention. This phase will serve to establish a stable baseline strength level before the athlete starts the rehabilitation program. Transition to Phase B will be determined by the strength variance between sessions; if there is a difference of ≤ 10% across the first three sessions for each leg, the athlete will move to Phase B at the fourth week. Otherwise, further testing sessions will be needed before the athlete starts the program, provided that a difference of ≤ 10% is achieved across three consecutive testing sessions.

In phase B, the athlete will perform a pain-guided progressive rehabilitation program which comprises three distinct components: anterior chain, posterior chain, and functional training. Anterior chain includes exercises relevant to the groin (adductor muscles, hip flexor muscles, and trunk muscles), posterior chain exercises targeting muscle groups not related to the injured area (hip extensor and abductor muscles, knee extensor and flexor muscles, and ankle plantar flexor muscles), and functional exercises related to the sport (hopping and jumping and linear running). The athlete will be allowed to choose between a number of exercises for each muscle group included in anterior and posterior chain components. Weekly training frequency will vary between 3 to 6 sessions, including 3 anterior chain sessions, 2-3 posterior chain sessions, and 2-3 functional training sessions, depending on the athlete's availability. Once specific return to sport criteria are fulfilled (Appendix II), Phase B will be completed.

During the rehabilitation period, the athlete will not be allowed to participate in any other form of training outside the predefined protocol. Additional upper limb exercises and any therapeutic options will be allowed after discussion with the research team, provided they do not interfere with the rehabilitation protocol implementation.

Exercise progression

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
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

  • Male or female long-distance runner
  • Long-standing groin pain (≥ 6 weeks)
  • ≥ 18 years

排除标准

  • - Neurological or musculoskeletal condition which do not allow the athlete to perform the strength testing and the program intervention.

研究组 & 干预措施

A single treatment

Experimental

干预措施: A pain-guided rehabilitation program (Other)

结局指标

主要结局

Return to sport time

时间窗: Return to sport time is determined as the time (number of days) from the first rehabilitation session to the day the athlete fulfils the return to sport criteria. The estimated time of the rehabilitation completion is up to 12 weeks.

The time to return to sport is defined as the total number of weeks recorded from the date of the first rehabilitation session to the day the athlete fulfils the return to sport criteria.

Adductor muscle strength

时间窗: Eccentric and isometric adductor muscle strength will be tested on weekly basis from baseline to the completion of the treatment. The estimated number of testing sessions throughout the intervention is 12.

Maximum eccentric and isometric adductor muscle strength will be assessed with a mid-range unilateral supine isometric adduction test and an outer-range unilateral supine eccentric adduction test, following standardized procedures which have demonstrated good intra-tester reliability \[EHAD ICC 0.91 (0.70-0.98), SEM: 6.3%, IHAD ICC 0.78 (0.30-0.95), SEM: 7.3%\]. Strength values will be normalized to the athlete's body weight and recorded as Nm/kg.

Tissue tolerance

时间窗: Tissue tolerance will be evaluated on weekly basis from baseline to the completion of the treatment. The estimated number of testing sessions throughout the intervention is 12.

Tissue tolerance is defined as the maximum adductor strength generated when the athlete reaches a pain level of 2/10 of the NPRS, and will be assessed with the use of a bilateral squeeze test at 0° of hip and knee flexion. Strength values will be normalized to the athlete's body weight and recorded as Nm/kg.

次要结局

  • Hip-related quality of life(Hip-related quality of life will be evaluated baseline and at the end of the rehabilitation. The estimated time for the intervention completion is 12 weeks.)
  • Athlete's recovery perception(Subjective overall recovery perception will be evaluated on a weekly basis. Although the overall duration of the intervention cannot be defined due to the criteria-based nature of the progression, the estimated time for completion is 12 weeks.)

研究者

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

Christos Pippas

PhDc, MSc, OMPT

University of West Attica

研究点 (1)

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