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临床试验/NCT06640699
NCT06640699尚未招募不适用

The Effects of Neurophysiological Facilitation Techniques on Cardiopulmonary Parameters After Coronary Artery Bypass Graft Surgery

Istanbul University - Cerrahpasa (IUC)0 个研究点目标入组 36 人开始时间: 2024年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
36
主要终点
ecocardiography device

研究概览

简要总结

The aim of the study is to investigate the effects of neurophysiological facilitation techniques, applied in addition to Phase I cardiac rehabilitation in the early postoperative period after coronary artery bypass graft (CABG) surgery, on left ventricular function, respiratory functions, and functional capacity.

详细描述

In this prospective randomized controlled study, participants will be randomly divided into two groups: the control group, which will receive Phase I cardiac rehabilitation, and the treatment group, which will receive Phase I cardiac rehabilitation along with the application of neurophysiological facilitation techniques. The participants' left ventricular function, respiratory functions, and functional capacity will be assessed before and after the interventions.

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
Double (Participant, Outcomes Assessor)

盲法说明

participants will be blind to groups, outcomes assessor will be blind to groups.

入排标准

年龄范围
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • First-time undergoing open-heart surgery
  • Aged between 50 and 85 years
  • Full cooperation

排除标准

  • Presence of facial, sternum, or rib fractures
  • Chronic renal failure
  • Development of cerebrovascular events
  • Cognitive function impairment
  • Development of deep vein thrombosis in the postoperative period
  • Presence of neuromuscular disease
  • Presence of orthopedic disabilities
  • Intubation duration longer than 24 hours
  • Staying in intensive care for more than 48 hours

结局指标

主要结局

ecocardiography device

时间窗: 3 months

ejection fraction will assess with ecocardiography.

spirometer

时间窗: 3 months

respiratory function test will assess with spirometer

6 Minutes walking test

时间窗: 3 months

functional capacity will assess with 6 minutes walk test.

次要结局

未报告次要终点

研究者

发起方
Istanbul University - Cerrahpasa (IUC)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gamze Aydin

Principal Investigator

Istanbul University - Cerrahpasa (IUC)

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