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Clinical Trials/ChiCTR2200064714
ChiCTR2200064714Not yet recruitingEarly Phase 1

肌内效贴联合减重步行训练对脑卒中患者步行功能的临床应用研究

单位自筹1 site in 1 country86 target enrollmentStarted: October 1, 2022Last updated:

Trial Snapshot

Phase
Early Phase 1
Status
Not yet recruiting
Sponsor
Enrollment
86
Locations
1
Primary Endpoint
偏瘫步行能力评定量表

Study Overview

Brief Summary

观察肌内效贴联合减重步行训练对脑卒中患者步行功能的影响

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照

Eligibility Criteria

Ages
20 to 60 (—)
Sex
All

Inclusion Criteria

  • 1.临床上诊断为脑卒中(脑出血、脑梗塞、脑栓塞);
  • 2.年龄 20-60 岁;
  • 3.Brunnstrom 分期<=3 期。

Exclusion Criteria

  • 1.严重认知、言语障碍;
  • 2.严重的心肺疾病不能参与活动;
  • 3.家属及患者不愿意参与。

Arms & Interventions

试验组

肌内效贴

对照组

常规康复训练后进行减重步行训练

Outcomes

Primary Outcomes

偏瘫步行能力评定量表

Time Frame: 干预前后

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
单位自筹

Study Sites (1)

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肌内效贴联合减重步行训练对脑卒中患者步行功能的临床应用研究 | Clinical Trial