Effects of Sensorimotor Insoles on Stability and Gait in Patients With Multiple Sclerosis. (SensorimotorMS)
研究概览
详细说明
This study is a single-blind, randomized controlled clinical trial designed to evaluate the long-term physiological and functional effects of sensorimotor insoles (SMIs) in individuals diagnosed with Multiple Sclerosis (MS).
Intervention Protocol and Device Customization Participants allocated to the experimental group receive custom-fabricated SMIs (Anatomy Line model, Springer Aktiv GmbH, Berlin, Germany). Digital foot models are generated using a mobile application (Foot Scan 3D) coupled with a specialized phone mirror device to capture three-dimensional foot morphology for custom orthosis manufacturing.
To ensure patient safety, promote acclimatization, and minimize potential adverse events, a structured 1-month adaptation protocol is implemented:
Adaptation Phase (Month 1): Participants wear the SMIs starting at 1 hour per day, increasing wear time by 1 hour every 3 days. SMI usage is initially restricted to indoor activities before expanding to outdoor use.
Maintenance Phase (Months 2-7): Following adaptation, participants wear the custom SMIs continuously during all daily activities within their habitual footwear.
The control group receives no study-specific insole intervention. To control for confounding rehabilitation effects, participants in both the experimental and control groups maintain their conventional, ongoing physical therapy regimens throughout the 7-month study period.
Evaluator Blinding and Site Logistics All outcome assessments take place at baseline and immediately following the 7-month intervention period at the facilities of the Asociación Vallisoletana de Esclerosis Múltiple. To maintain single-blind integrity, outcome evaluations are conducted by assessors who are fully masked to participant group assignment. Participant recruitment, randomization, and intervention monitoring are handled by independent research team members who do not perform outcome testing.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习地点
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Salamanca
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Salamanca、Salamanca、西班牙、37001
- Universidad de Salamanca
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Medical diagnosis of multiple sclerosis (MS), including relapsing-remitting, primary progressive, or secondary progressive subtypes.
- Age > 18 years.
- Expanded Disability Status Scale (EDSS) score between 2.0 and 6.0 (ranging from minimal disability to requiring a cane to walk).
- Signed written informed consent.
Exclusion Criteria:
- Cognitive impairment.
- Visual or vestibular disorders that could impair stability.
- Changes in disease-specific medication within the 2 months prior to study baseline.
- MS relapse within the 2 months prior to study baseline (for relapsing-remitting MS cases).
- Lower-limb capsuloligamentous injury within the 2 months prior to study baseline (such as ankle or knee sprains) that could affect stability or gait pattern.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Intervention group: use of sensorimotor insoles
Daily use of sensorimotor insoles for at least 5 hours per day over a 6-month period.
The insoles will be worn during activities of daily living or sports activities and are custom-designed for each participant.
At the beginning of the study, an adaptation period will be implemented during which insole wear time is progressively increased.
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Daily use of sensorimotor insoles for at least 5 hours per day over a 6-month period.
The insoles will be worn during activities of daily living or sports activities and are custom-designed for each participant.
At the beginning of the study, an adaptation period will be implemented during which insole wear time is progressively increased.
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无干预:Comtrol group
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Stability
大体时间:6 months
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Berg Balance Scale
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6 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Gait
大体时间:6 months
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Gait Assessment and Intervention Tool
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6 months
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Plantar cutaneous sensitivity
大体时间:6 months
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Pressure treshold
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6 months
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Ankle strength
大体时间:6 months
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Manual dynamometry
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6 months
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Function and Quality of life
大体时间:6 months
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Functional Assessment of Multiple Sclerosis
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6 months
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- INV2026-68
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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