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临床试验/NCT02697461
NCT02697461Unknown不适用

Multisegmented Foot Motion in Patients With Lateral Ankle Sprains and Chronic Ankle Instability

University of Virginia1 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2016年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
115
试验地点
1
主要终点
Changes in midfoot frontal plane range of motion during stance phase of gait.

研究概览

简要总结

Lateral ankle sprains (LAS) and chronic ankle instability (CAI) are common musculoskeletal injuries that are a result of inversion injury during sport. The midfoot is frequently involved during inversion injury, is often overlooked during clinical examination, and maybe contributory to the development of CAI. The purpose of this study is to investigate multisegmented foot motion using a motion capture system, clinical joint physiological and accessory motion, and morphologic foot measurements in recreationally active men and women with and without a history of lateral ankle sprains and chronic ankle instability. Additionally, the effects of a joint mobilization intervention in patients with diminished multisegmented foot motion and intrinsic foot strengthening in healthy individuals will be investigated.

详细描述

Arm 1:The purpose of this arm of the study is to determine if foot muscle exercises change the function of the foot. Up to 25 people will be enrolled in this arm of the study at the University of Virginia.

Arm 2: The purpose of this arm of the study is to determine if joint mobilization applied to the middle part of the foot will effect function in people who are healthy, have a history of lateral ankle sprains (LAS), or have chronic ankle instability (CAI) and have joint stiffness. Up to 125 people will be enrolled in this arm of the study at the University of Virginia. CAI is a condition where symptoms from an ankle sprain last longer than one year. These symptoms include a feeling of looseness, feelings that the participant may roll the ankle, or repeated ankle sprains. This study may help clinicians prescribe simple exercises at home to help treat CAI. The participants are being asked to be in this study, because they are physically active (participate in some form of physical activity for at least 20 minutes per day, three days per week) and are not currently seeking medical treatment/therapy for LAS/CAI. Joint mobilization is a commonly used clinical intervention used to decrease pain and increase joint range of motion. The home exercises employed for this study are commonly used clinically in the treatment of foot and ankle problems and include a foot and calf stretch and standing on one foot for 60 seconds. The participant will be asked to perform these exercises three times daily throughout the course of the day.

The investigators hypothesize that joint mobilization will improve patient oriented outcomes and measures of joint mobility and excursion in individuals with impaired foot mobility immediately post intervention and at 1-week follow-up, but not at 4 weeks; and intrinsic foot strengthening will result in differences in morphologic measures and intrinsic muscle cross-section in healthy individuals following a 4 week home exercise program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy participants
  • •Aged 18-50
  • •All subjects will be physically active: Participating in some form of physical activity for at least 20 min per day, three times per week.
  • •All subjects will have no history of ankle injury.
  • •LAS participants
  • •Aged 18-50
  • •All subjects with a history of ankle sprains, no lingering symptoms or disability, not actively receiving treatment for their ankle sprain
  • •All subjects will be physically active: Participating in some form of physical activity for at least 20 min per day, three times per week.
  • •CAI participants
  • •Aged 18-50
  • •CAI with a history of recurrent ankle sprains, with the first sprain occurring longer than 12 months ago. They will have lingering symptoms, and disability, but not actively receiving treatment for their CAI
  • •All subjects will be physically active: Participating in some form of physical activity for at least 20 min per day, three times per week.

排除标准

  • •Neurological or vestibular disorders affecting balance
  • •Currently seeking medical care for LAS/CAI
  • •History of prior ankle surgery
  • •History of ankle or foot fracture
  • •Diabetes mellitus
  • •Current self-reported disability due to lower extremity pathology that may adversely affect neuromuscular function
  • •Lumbosacral radiculopathy
  • •Soft tissue disorders including Marfan's syndrome and Ehlers-Dandros syndrome
  • •Absolute contraindications to manual therapy
  • •Pregnancy

研究组 & 干预措施

Intrinsic Foot Arm

Experimental

In arm 1, a randomized control trial will be used in the investigation of validity and reliability comparing multisegmented foot motion, clinical joint physiological and accessory motion, and morphologic foot measurements, and the effect of intrinsic foot strengthening on multisegmented foot function.

干预措施: Intrinsic Foot Strengthening (Other)

Joint Mobilization Arm

Experimental

In arm 2, the investigation of group differences in clinical and laboratory measures of multisegmented foot motion and kinetics will use a case control design. A randomized controlled trial will be conducted in the study investigating joint mobilization, with the researcher performing the assessments and the provider performing the treatments blinded to group allocation

干预措施: Joint Mobilization (Other)

结局指标

主要结局

Changes in midfoot frontal plane range of motion during stance phase of gait.

时间窗: Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks

Segmental motion will be assessed using motion capture and measured in degrees.

Changes in ultrasound thickness measures of the flexor digitorum brevis

时间窗: Arm 1: Baseline, 4 wks.

Muscle thickness measures will be measured in cm.

Changes in thickness measures of the flexor hallucis brevis

时间窗: Arm 1: Baseline, 4 wks.

Muscle thickness measures will be measured in cm.

Changes in ultrasound thickness measures of the abductor hallucis

时间窗: Arm 1: Baseline, 4 wks.

Muscle thickness measures will be measured in cm.

Foot and Ankle Ability Measure (FAAM)

时间窗: Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks

Patient Report Outcome of Foot and Ankle Function

次要结局

  • Changes in Foot morphological measurements across loading conditions(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of range of motion of first ray flexion/extension(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of ankle inversion strength(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Global Rate of Change (GROC)(Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of joint laxity of the forefoot(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Visual Analogue Scale (VAS)(Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of forefoot frontal plane range of motion(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of joint laxity of the first ray(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of toe flexor strength(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of ankle eversion strength(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of ankle dorsiflexion strength(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Changes in Clinical Measures of ankle plantarflexion strength(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Godin leisure questionnaire(Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • Star excursion balance test(Arm 1: Baseline, 1wk, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • 12-Item Short Form Survey from the RAND Medical Outcomes Study (VR-12)(Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks)
  • 11-item Tampa Scale of Kinesiophobia (TSK-11)(Arm 1: Baseline, 5 wks. Arm 2: Baseline, 1wk, 2wks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jay Hertel, PhD, ATC

Prinicipal Investigator

University of Virginia

研究点 (1)

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