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临床试验/NCT05859256
NCT05859256已完成不适用

Efficacy of a Flossing Protocol and Manual Therapy in the Clinical and Functional Improvement of Young Subjects With Recurrent Ankle Sprains. A Randomized Clinical Study.

Universidad Católica San Antonio de Murcia2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年5月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
2
主要终点
Change from baseline ankle range of motion after treatment and at 4 weeks

研究概览

简要总结

The most frequent lateral ankle sprain mechanism consists of talocrural plantarflexion added to a subtalar inversion. The anterior talofibular ligament, in plantar flexion, suffers maximum stress, being very sensitive to injury mechanisms with inversion of the foot, being the cause of up to 70% of sprains. The risk of injury recurrence must be taken into account. In sports practice, this percentage of recurrence is especially relevant.

Randomized clinical study. Participants will be randomized to a control or experimental group. The dependent variable will be the range of motion in ankle dorsiflexion. Secondary variables will be pressure pain threshold, and stability of the foot and ankle. Three evaluations will be carried out: before the start of the study (T0), after the intervention (T1) and after a 4-week follow-up period (T2). All evaluations will be performed by one evaluator, blinded to player assignment The intervention consists of the application of a treatment protocol based on an initial active warm-up consisting of 3 active exercises, walking for 1 minute performing slow and controlled movement of the ankle, raising the heels, 15 repetitions, dorsiflexion of the ankle in the standing position. gentleman, 15 reps. Subsequently, the floss band will be placed, performing again the 3 active warm-up exercises with the band on. After this, the passive manual techniques will be carried out for the remaining time, removing the flossing at the end of the latter, and actively mobilizing again.

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
Double (Participant, Outcomes Assessor)

盲法说明

All evaluations will be carried out by one evaluator, blinded to the study conditions and the assignment of the players to the two study groups.

In the subjects included in the control group, the same procedures will be carried out, but placing the flossing without tension and performing the Kaltenborn manual techniques without slipping and without joint mobilization.

入排标准

年龄范围
18 Years 至 22 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Young people between 18 and 22 years old
  • Who have suffered a previous sprain
  • No chronic or degenerative musculoskeletal pathologies of the ankle or knee
  • That they do physical activity regularly.

排除标准

  • Have suffered a sprain in the last 6 months
  • Being receiving another physiotherapy treatment at the time of the study
  • Not signing the informed consent document.

结局指标

主要结局

Change from baseline ankle range of motion after treatment and at 4 weeks

时间窗: Screening visit, within the first seven days after treatment and after four weeks follow-up

Using an analog goniometer, range of motion was measured. This instrument has shown excellent reliability. The joint range in plantar and dorsiflexion was measured. The unit of measurement is degrees (the higher the degree, the greater the mobility).

次要结局

  • Change from baseline foot and ankle stability after treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks follow-up)
  • Change from baseline pressure pain threshold treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks follow-up)

研究者

发起方
Universidad Católica San Antonio de Murcia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rubén Cuesta-Barriuso, PhD

Principal Investigator

Universidad Católica San Antonio de Murcia

研究点 (2)

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