Resistance Training for Patients Diagnosed With External Snapping Hip. A Feasibility Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 9
- 试验地点
- 6
- 主要终点
- Adverse events.
研究概览
简要总结
The purpose of this study is to investigate whether targeted progressive resistance training is safe and feasible for patients with external snapping hip. Dropout rates, adverse events and training adherence are investigated. The secondary purpose is to investigate whether it is possible through targeted progressive resistance training to improve participants' muscle strength, functional status and hip-related quality of life.
详细描述
Snapping hip (coxa saltans) is a disorder where the hip tends to make an audible click-through movement, often but not necessarily associated with pain. A prevalence of 5-10% of the general population has been reported. Snapping hip is divided into three forms of snapping hip; intraarticular, internal and external snapping hip. External snapping hip (coxa saltans external) is the most common form, and patients may experience pain when the iliotibial band or anterior part of the gluteus maximus slides over the greater trochanter at femur. Patients with external snapping hip are typically between 15 and 40 years, and physically active.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with Greater Trochanteric Pain Syndrome at the Orthopedic Surgery Department at Aarhus University Hospital in the period 2013-
- •In case of too few participants from this sample, we plan to include patients diagnosed during 2018
- •Minimum 18 years old
- •Able to read and understand Danish
- •Have experienced jump/click from the outside of the hip associated with pain within the last 14 days
- •Have a residence of a maximum of 55 km from Aarhus C
- •The participants must not have participated in regular resistance training of the hip muscles for more than 1 day per week in the last 6 months leading up to the start of the intervention
- •The participants must not have undergone a total hip replacement, a Periacetabular Osteotomy, a Z-plastic surgery or arthroscopy in the hip within 6 months before the start of the intervention or have a planned hip surgery during the intervention period
- •The participants must not suffer from neurological, rheumatological, metabolic or respiratory diseases that will influence the effect of the intervention
- •The participants must not have a planned vacation lasting more than 14 days during the intervention period, while not having the opportunity to extend the training period accordingly
排除标准
- •No longer suffering from external snapping hip
- •Pregnancy
结局指标
主要结局
Adverse events.
时间窗: Measured at each training session during the 12 week intervention.
A muscle or joint injury caused by the training program reported by a patient, or a canceled training session due to pain associated with exercise, or other harmful incidents associated with the training program.
Pain during exercise.
时间窗: Measured for each exercise performed during the 12 week intervention.
Pain during the exercises, measured by the Visual Analogue Scale (VAS). The score range from 0-10, where 0 means no pain and 10 means maximum pain
Adherence to the training.
时间窗: Measured during the 12 week intervention.
Measured by how many of the training sessions the participants completed. High adherence defined \>80% of completed sessions. Drop out is defined as a person included in the study who chooses to leave before the final test.
次要结局
- Change in muscle strength measured by dynamometer.(Measured at inclusion, two weeks after inclusion, and when the 12 week intervention has ended.)
- Change in hip function.(Measured at inclusion, two weeks after inclusion and when the 12 week intervention has ended.)
- Hypermobility status.(Measured at inclusion, two weeks after inclusion and when the 12 week intervention has ended.)
- Change in one repetition muscle strength.(At the start of the intervention and 12 weeks later at the end of the intervention.)
- Hip awareness.(Measured at inclusion, two weeks after inclusion and when the 12 week intervention has ended.)