Effects of a Hands Free Crutch on Walking Stability During Gait
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 21
- 试验地点
- 1
- 主要终点
- Whole Body Angular Momentum-sagittal Plane
研究概览
简要总结
The proposed study evaluates the effects of a hands free crutch (iWalkFree, Inc.) on walking balance and stability compared to standard crutches. It is expected that the hands free crutch will provide better stability during walking on a level surface and better reported balance confidence compared to standard crutches. In this study, walking stability will be assessed using motion capture data from an infrared camera system with 12 mounted cameras surrounding a level walkway. Balance will be assessed through a self-reported activity-specific balance confidence (ABC) questionnaire. An improved understanding of the effects of the hands free crutch on gait may benefit the future prescription of ambulatory assistive devices. The proposed study may provide insight that can be used by physical therapists and other providers to select the ambulatory assistive device that best meets their patients' needs.
详细描述
The purpose of this study is to compare the hands free crutch (HFC) to standard axillary crutches (SACs) with and without a walking boot, using outcomes related to walking stability, balance confidence, patient preference, device comfort, and any reported pain while using the devices.
Healthy, able-bodied individuals will wear a walking boot to simulate a below knee injury or post-surgery condition during participation. They will maintain a non-weight bearing status while completing the 4 research conditions in randomized order: 1) BOOT, 2) HFC + BOOT, 3) SAC + BOOT, or 4) NONE.
Participants will complete 5 total sessions, with 4 biomechanics data collection sessions corresponding to the 4 conditions. At the first visit, participants will complete pre-consent screening and consent paperwork. Then they will be randomized to the 4 conditions above, and anthropometric (body height, weight/mass, leg length, shoe length and width) and demographic data will be collected. Participants will accommodate overnight to each of the 4 study conditions before testing. If participants are randomized to the NONE condition first, they will have the option of completing testing in that condition (no Boot) at the initial visit. The primary dependent measure is whole body angular momentum, an objective measure of walking stability.
Data will be collected using over 50 small reflective markers placed on the participants and the assistive devices, a computerized motion capture system and force plates embedded in the floor. The force plates capture ground reaction forces which will be used to calculate joint moments for interpretation of angular momentum data. The motion capture system will be used to evaluate joint and segment kinematics and temporal-spatial data to characterize the gait pattern in each condition and calculate angular momentum.
The second purpose of this research study is to determine the effect of crutch use on participant reported balance confidence and device preference. A validated balance confidence questionnaire and participant satisfaction, comfort and preference will be used to compare between conditions. A numerical pain rating scale (0-10) will be used to assess for any reported pain in all of the conditions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male or Female
- •Ages: 18 - 45
- •Height between 5'2" and 6'6"
- •Foot size that corresponds to available walking boots
- •Healthy individuals without current complaint of lower extremity pain, spine pain, open wounds or active infection
- •Full active pain free range of motion of the bilateral upper and lower extremities and spine
- •Able to hop without pain
- •Able to perform a full squat without pain
- •Able to walk up and down a flight of stairs at normal walking speed without using the hand rail
- •Able to stand on one leg for at least 30 seconds
- •Able to read and write in English and provide written informed consent
排除标准
- •Weight greater than 270 lbs
- •BMI greater than 35
- •Maximum thigh circumference at top of the leg greater than 28"
- •Prior medical or neuromusculoskeletal disorders that have limited their participation in work or exercise in the last 6 months
- •Prior lower extremity injury proximal to the ankle requiring surgery or limiting function for greater than 6 weeks
- •Prior back pain that recurs or has limited activities for greater than 6 weeks
- •Diagnosed moderate or severe brain injury
- •Diagnosis of a physical or psychological condition that would preclude testing (e.g. cardiac condition, clotting disorder, pulmonary condition)
- •Uncorrected visual or hearing impairment(s)
- •Require use of an assistive device
- •Pregnancy - Per participant self-report. Due to the expected small number of pregnant individuals, and resulting inability to account for its effect on resulting outcomes, participants will be withdrawn from the study
研究组 & 干预措施
Arm 1. NONE
Participants will be tested while wearing no boot and no assistive device.
Arm 2. BOOT
The first intervention condition tested is a walking boot only on the subject's right lower extremity.
干预措施: BOOT (Device)
Arm 3. HFC+BOOT
The second intervention condition tested is a Hands Free Crutch (HFC) with the walking boot, both worn on the subject's right lower extremity.
干预措施: HFC+BOOT (Device)
Arm 4. SAC+BOOT
The third intervention condition tested is standard axillary crutches (SAC) with the walking boot worn in non-weight bearing on the subject's right lower extremity.
干预措施: SAC+BOOT (Device)
Arm 5. HFC
The fourth intervention condition tested is the Hands Free Crutch worn on the subject's right lower extremity without the walking boot.
干预措施: HFC (Device)
Arm 6. SAC
The fifth and last intervention condition tested is standard axillary crutches with the subject non-weight bearing on the right lower extremity without the walking boot.
干预措施: SAC (Device)
结局指标
主要结局
Whole Body Angular Momentum-sagittal Plane
时间窗: one session (up to 2 hours long), out of 4 total sessions
Range of whole-body angular momentum in the sagittal plane during gait using the motion capture system. While angular momentum can be measured in kg\*m\^2/second it is reported as dimensionless in this study as it has been normalized to body weight (kg), height (m), and walking speed (m/s).
次要结局
未报告次要终点
研究者
Jason Wilken
Associate Professor of Physical Therapy and Rehabilitation Science
University of Iowa