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).
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