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临床试验/NCT06453798
NCT06453798招募中不适用

Effect of Cervical Exercise Combined With Nerve Mobilization on Cervical Spondylotic Radiculopathy

Quanzheng Chen1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年7月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Visual analogue scale

研究概览

简要总结

The objective of this clinical trial was to investigate the effects of cervical spine exercises combined with nerve mobilization in patients with radiculopathy.

The main questions it aims to answer are:

  1. Whether cervical spine operation combined with nerve mobilization is effective for cervical radiculopathy.
  2. Is there any difference between cervical spine operation combined with nerve mobilization and single method? The participants were patients with cervical radiculopathy and were divided into three groups in this study.

1. Experimental group: received cervical spine operation combined with nerve mobilization 2. Control group 1: cervical spine exercises were performed 3. Control group 2: received neuromobilization

详细描述

After being informed of the risks, participants are required to sign an informed consent form. Eligible participants will be randomly assigned to cervical spine operation combined with nerve mobilizatio or cervical spine exercises or neuromobilization on a 1:1:1 ratio.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meet the diagnostic criteria of CSR and have no other complications;
  • Age 18-65 years old, gender unlimited;
  • No other treatment for cervical spondylosis in the last 1 month;
  • No previous surgical treatment for cervical spondylosis;
  • Good compliance;
  • Good mental state, no history of mental illness;
  • Informed consent, and sign the informed consent.

排除标准

  • does not meet the diagnostic criteria;
  • Women during pregnancy;
  • severe stenosis of the foramen;
  • osteoporosis combined with spinal cord tumor, osteomyelitis;
  • infectious diseases, skin defects, allergies;
  • have serious heart, lung and other important organ dysfunction;
  • unable to cooperate.

结局指标

主要结局

Visual analogue scale

时间窗: baseline and 4 weeks

A scale used to evaluate pain. The scale consists of 0 to 10 points, with a higher score indicating greater pain and a lower one.

Range of motion

时间窗: baseline and 4 weeks

The range of motion of the associated joints in the neck was measured using a joint protractor

Muscle strength

时间窗: baseline and 4 weeks

The microFET2 instrument was used to test the muscle strength of the neck related muscles.

次要结局

  • Tanaka Yasuhisa Cervical Spondylopathy Symptom Scale(baseline and 4 weeks)
  • the medical outcomes study 36-item short-form health survey(baseline and 4 weeks)
  • neck disability index. The total score ranges from 0 (accessibility) to 50 (total paralysis), with higher scores indicating more severe dysfunction.(baseline and 4 weeks)

研究者

发起方
Quanzheng Chen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Quanzheng Chen

Primary rehabilitation therapist

Lingshan County second People's Hospital

研究点 (1)

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