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临床试验/NCT04619784
NCT04619784Unknown不适用

The Effect of Pilates Application on Abdominal Muscle Function, Core Stability, Musculoskeletal Pain, Quality of Life, Anxiety and Depression in Parkinson's Patients

Dokuz Eylul University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
20
试验地点
1
主要终点
Muscle Function

研究概览

简要总结

In this study, it is aimed to investigate the effect of Pilates application on abdominal muscle function, core stability, musculoskeletal pain, quality of life, anxiety and depression in Parkinson's Patients.

详细描述

Objective

In this study, it is aimed to investigate the effect of Pilates application on abdominal muscle function, core stability, musculoskeletal pain, quality of life, anxiety and depression in Parkinson's Patients.

Method: The study included 15 Idiopathic Parkinson's Patients over 18 years of age, under stage 3 according to the Hoehn-Yahr clinical staging. Patients were divided into intervention and control groups. Pilates training was performed for 6 weeks, twice a week and 60 minutes per session in intervention group. Demographic features will be questioned and recorded in the data recording form through mutual interview in patients who meet the inclusion criteria; evaluations will be made regarding muscle thickness and pain. All patients will be evaluated before treatment, after treatment, at the 3rd and 6th months.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •Diagnosed with Idiopathic Parkinson's Disease
  • •Must be older 18 years old
  • •Must have 24 and above score on Mini Mental Test
  • •Must be the third or lower stage according to the Hoehn-Yahr staging
  • •Must have stable clinical status

排除标准

  • •Musculoskeletal or cognitive impairment at a level affecting evaluation and treatment
  • •Other neurological disease

研究组 & 干预措施

Treatment Group

Experimental

Demographic features will be questioned and recorded in the data recording form through face to face interview in patients who meet the inclusion criteria; evaluations will be made regarding muscle thickness and pain. Patients will receive 12 sessions of pilates. Patients will be evaluated before treatment, after treatment, at the 3rd and 6th months.

干预措施: Pilates Exercises (Other)

Control Group

Other

Demographic features will be questioned and recorded in the data recording form through face to face interview in patients who meet the inclusion criteria; evaluations will be made regarding muscle thickness and pain. Their routine medical treatments were continued

干预措施: control (Other)

结局指标

主要结局

Muscle Function

时间窗: Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment

Muscle thickness measurement will be used to evaluate the function of transversus. Ultrasonography with a linear transducer (MHz) will use to measure the Transversus Abdominis thickness both at rest and during the abdominal drawing-in maneuver (ADIM). During ADIM, participants will be asked to abdominal hollowing which will be a gentle voluntary contraction of abdominal wall. All images are obtained at the end of expiration not to allow the effect of respiration on muscle thickness. Three measures are recorded in the both condition. The average values of measures are used in the data analysis.

次要结局

  • Anxiety(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment)
  • Core stability(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment)
  • Musculoskeletal Pain(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment)
  • Quality of Life(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment)
  • Depression(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment.)
  • Pain intensity(Patients will be evaluated before treatment, 1 week after treatment, at the 3rd and 6th months after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Evrim Goz

Research assistant

Dokuz Eylul University

研究点 (1)

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