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Sleep Quality Response to Resisted Training After Coronary Artery Bypass Grafting (exercises)

2019年2月21日 更新者：Hady Atef Labib、Cairo University
Background:There are still many gaps in research concerning the effect of different physical training modalities on sleep quality in the population underwent coronary artery bypass graft surgeries(CABG).Purpose:The present study was conducted to compare the quality of sleep in subjects who underwent CABG, were submitted to two types of training (i.e, aerobic exercise alone or combined aerobic and resistance training

研究概览

地位

完全的

条件

干预/治疗

详细说明

OBJECTIVE/BACKGROUND:

There are still many gaps in research concerning the effect of different physical training modalities on sleep quality in the cardiac population. Thus, the objective of the present study was to compare the quality of sleep in subjects who underwent coronary artery bypass surgery submitted to two types of training (ie, aerobic exercise alone or combined aerobic and resistance training).

PATIENTS/METHODS:

80 Participants aged 45-65 years were randomized to two groups: aerobic group (AG), combined aerobic and resistance group (ARG). Training lasted ten consecutive weeks with 30 uninterrupted sessions. The actigraph (Actiwatch Minimitter Company, Incorporated (INC) - Sunriver, OR, USA) was placed on the non-dominant wrist and activities were monitored continuously while being recorded at one minute intervals. The participants kept the device for a period of 96 hours before the first and last training sessions.

研究类型

介入性

注册 (实际的)

80

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。

学习地点

  • 埃及
    • Cairo
      • Giza、Cairo、埃及、11262
        • National Heart Institute

参与标准

研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

45年 至 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Patients who have underwent CABG surgery since 6-8 weeks
  2. Their ages ranges from 40 and 80 years of age
  3. Medically stable patients.
  4. patients did CABG-only treatment (not combined with valve replacement surgery)
  5. Current complaint of poor Sleep quality (SQ) (score > 5 of the SQ scale)
  6. Body mass index ≤ 35 kg/m2 (no obstructive sleep apnea)

Exclusion Criteria:

  1. Any patient is known to have any unstable medical condition
  2. History of chronic insomnia for at least one year before surgery
  3. Indication of receiving treatments for depression and anxiety
  4. Musculoskeletal or neurological conditions that might interfere with the execution or the assessment of the exercise.

学习计划

本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。

研究是如何设计的？

设计细节

  • 主要用途：预防
  • 分配：随机化
  • 介入模型：并行分配
  • 屏蔽：单身的

武器和干预

参与者组/臂
干预/治疗
有源比较器：aerobic exercise group

aerobic exercises (intervention) on treadmill for 10 weeks, 3 times/week for duration of 30-45 min/session.

Exercise intensity is 50-65%of maximal heart rate (MHR)
行为的：exercise
control group (n=40) did aerobic exercises on treadmill for 10 weeks experimental group (n=40) did combined aerobic and resisted exercises for 10 weeks
其他名称：
  • 心脏康复
实验性的：aerobic and resisted exercise
combined resisted and aerobic exercises (intervention) for 10 weeks (circuit weight training and treadmill training respectively) 2 times/week for a duration of 30-45 min/session Exercise intensity is 50-65%of maximal heart rate (MHR) for aerobic part and 50% of 1 repetition maximum (1RM) for resistance part.
行为的：exercise
control group (n=40) did aerobic exercises on treadmill for 10 weeks experimental group (n=40) did combined aerobic and resisted exercises for 10 weeks
其他名称：
  • 心脏康复

研究衡量的是什么？

主要结果指标

结果测量
措施说明
大体时间
sleep quality to be assessed by Pittsburgh Sleep Quality Index (PSQI)
大体时间：up to 12 months
1.The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval.
up to 12 months
sleep fragmentation index to be assessed by actigraphy
大体时间：up to 12 months
2.Actigraphy is a valid tool to assist in determining sleep patterns in normal, healthy adult populations, normal infants and children, and patients suspected of certain sleep disorders.
up to 12 months

次要结果测量

结果测量
措施说明
大体时间
Functional aerobic capacity to be assessed by 6 minute walk test (6MWT)
大体时间：6 months
The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.
6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

Cairo University

调查人员

  • 首席研究员：Hady Atef, Master、Assistant lecturer of physical therapy,Cairo University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2018年1月1日

初级完成 (实际的)

2018年4月1日

研究完成 (实际的)

2018年7月1日

研究注册日期

首次提交

2019年2月15日

首先提交符合 QC 标准的

2019年2月21日

首次发布 (实际的)

2019年2月26日

研究记录更新

最后更新发布 (实际的)

2019年2月26日

上次提交的符合 QC 标准的更新

2019年2月21日

最后验证

2019年2月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • Sleep and Exercise

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)？

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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