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临床试验/NCT07384858
NCT07384858已完成不适用

Effects of Attentional Focus Strategies During Isokinetic Quadriceps Training on Strength and Functional Performance in Individuals With Patellofemoral Pain Syndrome.

Istanbul University - Cerrahpasa2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年2月2日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36
试验地点
2
主要终点
Kujala Patellofemoral Pain Score

研究概览

简要总结

Patellofemoral pain syndrome (PFPS) is a multifactorial musculoskeletal condition that is common particularly among young and physically active individuals, negatively affecting activities of daily living and physical performance. Although exercise therapy is considered the gold standard in the management of PFPS, there is limited evidence regarding the effectiveness of motor learning strategies applied during exercise. This study aims to shed light on how motor learning approaches can be optimized in clinical rehabilitation by comparing the effects of internal and external focus strategies used during exercise on muscle activation, functional performance, and pain.

This research will make a methodological contribution to the literature through the objective evaluation of muscle mechanical properties using isokinetic assessment and the MyotonPRO device. The findings are expected to clarify the effects of attentional focus strategies on therapeutic outcomes in PFPS rehabilitation and have the potential to provide an evidence-based guide for physiotherapy practice. In this way, the study may contribute to the development of new approaches aimed at improving both clinical effectiveness and patient adherence.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Aged between 18 and 45 years.
  • Diagnosed with patellofemoral pain syndrome (PFPS).
  • Anterior or retropatellar knee pain persisting for at least four weeks with a VAS score >
  • Pain exacerbated by at least two functional activities (e.g., squatting, stair climbing, prolonged sitting).
  • Willing to regularly participate in the 6-week program throughout the study period.

排除标准

  • History of patellar subluxation or dislocation.
  • Anterior or posterior cruciate ligament insufficiency.
  • Lower extremity fractures.
  • Neurological or systemic musculoskeletal disorders.
  • Rheumatoid arthritis or other inflammatory joint diseases.
  • History of knee surgery, meniscal injury, or any other underlying musculoskeletal condition that would prevent the participant from performing the exercises.
  • Pregnancy or postpartum period.
  • Participation in a similar exercise program within the last 3 months.
  • Radiographic evidence of osteoarthritis classified as Kellgren-Lawrence grade 2 or higher.

研究组 & 干预措施

Internal focus

Experimental

干预措施: Internal focus group (Other)

External focus

Experimental

干预措施: External focus (Other)

结局指标

主要结局

Kujala Patellofemoral Pain Score

时间窗: baseline

Kujala Patellofemoral Pain Score is a valid and reliable self-reported outcome measure specific to patellofemoral pain syndrome that assesses knee function and pain-related limitations during daily activities. The total score ranges from 0 to 100, with higher scores indicating better knee function and fewer symptoms.

Kujala Patellofemoral Pain Score

时间窗: Week 3 of the Treatment

Kujala Patellofemoral Pain Score is a valid and reliable self-reported outcome measure specific to patellofemoral pain syndrome that assesses knee function and pain-related limitations during daily activities. The total score ranges from 0 to 100, with higher scores indicating better knee function and fewer symptoms.

Kujala Patellofemoral Pain Score

时间窗: Week 6 of the Treatment

Kujala Patellofemoral Pain Score is a valid and reliable self-reported outcome measure specific to patellofemoral pain syndrome that assesses knee function and pain-related limitations during daily activities. The total score ranges from 0 to 100, with higher scores indicating better knee function and fewer symptoms.

次要结局

  • Visual Analog Scale(baseline)
  • Visual Analog Scale(Week 3 of the Treatment)
  • Visual Analog Scale(Week 6 of the Treatment)
  • Isokinetic Muscle Strength Assessment (Isoforce)(baseline)
  • Isokinetic Muscle Strength Assessment (Isoforce)(Week 3 of the Treatment)
  • Isokinetic Muscle Strength Assessment (Isoforce)(Week 6 of the Treatment)
  • Muscle Tone(baseline)
  • Muscle Tone(Week 3 of the Treatment)
  • Muscle Tone(Week 6 of the Treatment)
  • Muscle Stiffness(baseline)
  • Muscle Stiffness(Week 3 of the Treatment)
  • Muscle Stiffness(Week 6 of the Treatment)
  • Muscle Elasticity(baseline)
  • Muscle Elasticity(Week 3 of the Treatment)
  • Muscle Elasticity(Week 6 of the Treatment)
  • Step-Down Test(baseline)
  • Step-Down Test(Week 3 of the Treatment)
  • Step-Down Test(Week 6 of the Treatment)
  • Single-Leg Hop Test(baseline)
  • Single-Leg Hop Test(Week 3 of the Treatment)
  • Single-Leg Hop Test(Week 6 of the Treatment)

研究者

发起方
Istanbul University - Cerrahpasa
申办方类型
Other
责任方
Principal Investigator
主要研究者

Seda Ateş

physiotherapist

Istanbul University - Cerrahpasa

研究点 (2)

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