跳至主要内容
临床试验/NCT03104049
NCT03104049已完成不适用

Pilot Study on the Effects of Neuromuscular Taping in Parkinson's Disease Patients

IRCCS San Raffaele Roma0 个研究点目标入组 46 人开始时间: 2015年11月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
46
主要终点
Change in the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) rating scale total score between baseline evaluations and end of treatment

研究概览

简要总结

Parkinson's disease (PD) is a degenerative disorder characterized by a symptom triad consisting on: tremor, rigidity and bradykinesia . To these symptoms it is often added postural alteration that can stand in two different attitudes, such as the camptocormia and the syndrome of Pisa . Progressing in its evolution, PD becomes increasingly disabling, making it difficult or even impossible daily activities such as washing or dressing.The abnormal posture, with alteration of the limbs, the neck and trunk, is a recurring feature in PD, with a frequency of about 30%. Between 2% and 12.3% are more severe abnormalities such as camptocormia, the syndrome of Pisa and the anterocollis. Several studies disease plug in Neuromuscular Taping technique (NMT) among rehabilitative tools in degenerative neurological syndromes.

To the best of our knowledge, no applications were found in PD. Therefore, the current study was designed to evaluate quantitatively the effects of the NMT intervention on the trunk kinematics during standing position. More specifically, this study aims to compare the trunk kinematic variables of patients with PD who were treated with effective NMT versus those of the subjects who received only the pharmacological treatment.

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
Single (Investigator)

入排标准

年龄范围
60 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of idiopathic PD by United Kingdom Brain Bank criteria
  • No other significant neurological or orthopedic problems
  • Age between 55 and 80 years
  • MDS-UPDRS item 3.13 Posture between mild and moderate (definite flexion, scoliosis or leaning to one side)
  • Patient able to walk independently or with minimal assistance for 10 meters
  • Medical treatment for Parkinson's Disease must be stable for at least two weeks prior to inclusion, and during the study. During the study, the dosage of anti-parkinsonian drug treatment should not change, if it is not deemed necessary by the investigator.

排除标准

  • Disability to understand instructions required by the study (Informed Consent Test of Comprehension)
  • primarily wheelchair bound
  • Skin abrasions
  • sensitive skin

结局指标

主要结局

Change in the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) rating scale total score between baseline evaluations and end of treatment

时间窗: baseline and end of treatment (1 month)

Clinical measures were summarized as means and standard deviations for all the 46 patients.

次要结局

  • Change in the EuroQol 5 total score between baseline evaluations and end of treatment(baseline and end of treatment (1 month))
  • Change in the Non Motor Symptoms scale total score between baseline evaluations and end of treatment(baseline and end of treatment (1 month))
  • Change in the Freezing of Gait total score between baseline evaluations and end of treatment(baseline and end of treatment (1 month))
  • Change in the Parkinson Disease Quality of life 8 total score between baseline evaluations and end of treatment(baseline and end of treatment (1 month))

研究者

发起方
IRCCS San Raffaele Roma
申办方类型
Other
责任方
Sponsor

相似试验