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临床试验/NCT07544940
NCT07544940尚未招募不适用

Digital Health-Based Rehabilitation for Participants With Patellofemoral Pain

Chengdu Sport University0 个研究点目标入组 40 人开始时间: 2026年5月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
主要终点
Anterior Knee Pain Scale

研究概览

简要总结

This randomized controlled superiority trial will compare a 6-week digital health rehabilitation program with a 6-week self-guided exercise program in adults with patellofemoral pain. Assessments will be performed at baseline, 6 weeks, and 18 weeks. The primary outcome will be change in AKPS from baseline to 6 weeks. Secondary outcomes will include pain intensity, self-reported function, psychological outcomes, quality of life, muscle strength, adherence, and adverse events.

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

  • Age 18-45 years
  • Clinical diagnosis of patellofemoral pain
  • Symptoms for at least 3 months
  • Anterior or retropatellar knee pain provoked by at least two aggravating activities such as stair ambulation, squatting, running, jumping, or prolonged sitting
  • Baseline pain intensity of at least 3/10 on the Numeric Rating Pain Scale
  • Ability to provide written informed consent and comply with study procedures

排除标准

  • Previous knee surgery
  • Patellar dislocation or obvious instability
  • Ligament injury, clinically important meniscal injury, moderate to severe knee osteoarthritis, or other major structural knee pathology
  • Major hip, ankle, or lumbar disorders substantially affecting lower-limb function
  • Neurological disorders affecting movement or balance
  • Pregnancy
  • Structured PFP rehabilitation within the previous 3 months
  • Any other condition deemed unsuitable by the investigators

研究组 & 干预措施

Control group

Active Comparator

干预措施: Self-guided exercise (Behavioral)

Digital health group

Experimental

干预措施: Digital health (Behavioral)

结局指标

主要结局

Anterior Knee Pain Scale

时间窗: Baseline; 6 weeks; 18 weeks

次要结局

  • Muscle strength(Baseline; 6 weeks; 18 weeks)
  • Knee injury and Osteoarthritis Outcome Score(Baseline; 6 weeks; 18 weeks)
  • Tampa Scale for Kinesiophobia(Baseline; 6 weeks; 18 weeks)
  • Pain Catastrophizing Scale(Baseline; 6 weeks; 18 weeks)

研究者

发起方
Chengdu Sport University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wei-yang Zhang

Assistant Professor

Chengdu Sport University

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