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临床试验/PACTR202209718136908
PACTR202209718136908招募中2 期

The effectiveness of pain neuroscience education in the treatment of recreational marathon runners with chronic running related knee injuries

Tyren Naidoo0 个研究点目标入组 60 人开始时间: 2022年7月19日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • Inclusion Criteria
  • Signed informed consent.
  • Participants aged 18 to 65 years (Knechtle and Nikolaidis 2018; Larsen et al. 2020).
  • Participants who are male or female with symptomatic chronic knee pain (greater than 3 months duration).
  • Participants with a weekly training volume between 30 and 80km/week (Rasmussen et al. 2013).
  • Participants who had completed 2 or more marathon events within the past 2 years (virtual and non-virtual).
  • Participants with a score greater than 40 on the central sensitization inventory scale (CSI) (Mayer et al. 2012).

排除标准

  • Exclusion Criteria
  • Professional and elite marathon runners (Rüst et al. 2011).
  • Participants who have had previous total knee replacement or any other lower limb surgery within the past six months of the affected knee, co-existing inflammatory, metabolic or neurologic disease (Messier et al. 2008; Lluch et al. 2018).
  • Participants who have contraindications to chiropractic care and PNE.
  • Participants who have previously received chiropractic care and/or PNE can require a 3 month wash out period before they can be eligible to enter the study.
  • Participation in other pain trials prior (3 months) to recruitment.
  • Lack of the ability to adhere to the protocol, cognitive impairment, illiteracy or unable to speak English (Lluch et al. 2018).

研究者

发起方
Tyren Naidoo

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