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临床试验/NCT06073899
NCT06073899招募中不适用

Biopsychosocial Factors in Resistance Exercise in Individuals With Knee Pain

University of Central Florida2 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2024年1月16日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
57
试验地点
2
主要终点
Pressure Pain Threshold

研究概览

简要总结

The purpose of this research is to examine changes in pain sensitivity during high fatigue exercise, low fatigue exercise, and no treatment in individuals who are currently experiencing knee pain. Dosing dynamic resistance exercise intensity based on fatigue level is a novel, clinically feasible method. Dynamic resistance exercise at a high intensity (75% 1 repetition maximum (RM)) produces significant hypoalgesia at local sites compared to no treatment; however, dosing intensity based on 1RM can be challenging to implement in the clinical setting. Fatiguing endurance tasks produce local and systemic reductions in pressure pain threshold with low intensity isometric exercise completed until failure resulting in the largest exercise induced hypoalgesia effects. Fatigue may be an important mediator in pain response to exercise.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Investigator)

盲法说明

Investigator administering Pressure Pain Threshold will be blinded to the intervention.

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Experiencing knee pain symptom intensity rated as 3/10 or higher in the past 24 hours

排除标准

  • non-English speaking
  • history of knee surgery or fracture within the past 6 months
  • history of quadriceps tendon rupture
  • history of a chronic pain condition, such as fibromyalgia
  • systemic medical conditions that affect sensation, such as uncontrolled diabetes or neurological conditions
  • blood clotting disorder, such as hemophilia
  • known presence of cardiovascular, pulmonary, or metabolic disease
  • current use of tobacco products
  • contraindication to the application of ice, including blood pressure over 140/90 mmHg, -conditions that cause hives or blood in urine when exposed to cold, and any reductions in blood flow to arms or legs.
  • not physically ready to exercise without a medical exam as indicated by the Physical Activity Readiness Questionnaire + (PAR-Q+)
  • pain during active knee range of motion 0-90 degrees (examined during screening)
  • unable to attend 4 sessions

结局指标

主要结局

Pressure Pain Threshold

时间窗: This procedure will be completed two times before and after each set of exercise with the average analyzed. Outcomes are examined during each intervention visit from enrollment to study completion, about 2 years.

A computerized pressure algometer (AlgoMed, Ramat Yishai, Israel) with a 1 cm diameter rubber tip will be applied at a constant rate. Participants will be instructed to say 'stop' or 'pain' or press a response button connected to the algometer so that stimulus can be terminated when the sensation first changes from pressure to pain (pain threshold). This will be applied to the quadriceps and upper trapezius on the same side as the participant's knee pain.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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