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临床试验/NCT03348605
NCT03348605Unknown不适用

Descriptive Study of Receptive Fields in Lower Limb Amputees and the Effect of a Related Stimulation System on Selected Gait Parameters

Rehaklinik Bellikon2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2017年10月27日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
35
试验地点
2
主要终点
Description of receptive Fields Size in cm2

研究概览

简要总结

It has been observed that patients subjected to amputations develop so called receptive fields, which time of occurrence and localization over time are yet not examined systematically.

This clinical trial aims to investigate the reliability in detecting these receptive fields as well as their incidence and changes over time.

Further it aims to evaluate the acute effect of a stimulating system ("Phantom Stimulator" (Cort X Sensorics, Spaichingen, Germany)) on selected gait parameters measured tough a gait analysis system ("OprtoGait" (Microgate, Bolzano, Italy)) as well as on phantom sensations measured through a questionnaire.

详细描述

It has been observed that patients subjected to amputations develop so called receptive fields, which time of occurrence and localization over time are yet not examined systematically.

A receptive field is defined as skin area anywhere on the same side of the body as the amputation, which when stimulated by others, causes phantom sensations in the amputated extremity.

This clinical trial aims to investigate the reliability in detecting these receptive fields as well as their incidence and changes over time.

Further it aims to evaluate the acute effect of the stimulating system ("Phantom Stimulator" (Cort X Sensorics, Spaichingen, Germany)) on selected gait parameters measured tough a gait analysis system ("OprtoGait" (Microgate, Bolzano, Italy)) as well as on phantom sensations measured through a questionnaire.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Screening
盲法
Single (Participant)

盲法说明

As this study is described as single blinded, the only entity of the trial not aware of the group or sequence of the participant is the participant itself.

The other personell involved in the trial needs to be aware of the position of the participant within the study so to apply the right measures.

In this case the participant is unaware of the fact whether his stimulation system is turned on or off.

入排标准

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

入选标准

  • Inclusion criteria for descriptive study:
  • a. Lower limb amputation (independently of side or height of amputation)
  • Inclusion criteria for Phantom stimulator:
  • Receptive fields present at testing day 31 (last regular assessment of the receptive fields)
  • Lower limb amputation below the knee (if both sides the system is applied to the dominant side).

排除标准

  • Implanted devices (defibrillator or pacemaker)

结局指标

主要结局

Description of receptive Fields Size in cm2

时间窗: 4-5 Weeks (7 hours)

The primary outcomes are the changes in size over time. Here the size is described in cm2. The Fields size will be recorded by drawing them on the skin with eyeliner and subsequently taking photos. Later, these photos are analysed with the computer program Photoshop.

Description of receptive Fields Position in % overlapping from first measurement

时间窗: 4-5 Weeks (7 hours)

The primary outcomes are the changes in Position over time. Here the position is described in % overlapping with respect to the first measurement. The Fields position will be recorded by drawing them on the skin with eyeliner and subsequently taking photos. Later, these photos are put together and compared with the computer program Photoshop.

次要结局

  • Change in gait parameters through Phantom Stimulator(1/2 Day (3 hours))
  • Change in phantom sensations through Phantom Stimulator(1/2 Day (3 hours))

研究者

发起方
Rehaklinik Bellikon
申办方类型
Other
责任方
Sponsor

研究点 (2)

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