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Clinical Trials/ChiCTR2100046594
ChiCTR2100046594Active, not recruitingEarly Phase 1

基于运动监测的腰椎固定融合术后居家康复影响因素的分析及干预研究

上海市卫健委1 site in 1 country60 target enrollmentStarted: January 1, 2022Last updated:

Trial Snapshot

Phase
Early Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
改良巴氏指数

Study Overview

Brief Summary

1.分析影响腰椎固定融合术后居家康复的关键因素; 2.探索基于运动监测的腰椎固定融合术后居家模式。

Study Design

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

Eligibility Criteria

Ages
25 to 80 (—)
Sex
All

Inclusion Criteria

  • 1.诊断明确并完成手术者;

Exclusion Criteria

  • 2.有严重心、肺、肾疾病者。

Arms & Interventions

试验组

在康复门诊定期随访的基础上,基于运动监测的家庭康复

对照组

在康复门诊定期随访基础上,普通居家康复。

Outcomes

Primary Outcomes

改良巴氏指数

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
上海市卫健委

Study Sites (1)

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