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临床试验/NCT03470246
NCT03470246招募中不适用

Personalized Intervention to Increase Physical Activity and Reduce Sedentary Behaviour in Rehabilitation After Cardiac Operations (the PACO Trial)

Kuopio University Hospital1 个研究点 分布在 1 个国家目标入组 540 人开始时间: 2018年4月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
540
试验地点
1
主要终点
Improvement in mean daily number of steps

研究概览

简要总结

The PACO trial is a randomized clinical trial conducted in Heart Centers of Kuopio and Turku university hospitals. The coronary artery disease, aortic valve stenosis and mitral valve insufficiency patients preparing for elective coronary artery bypass grafting (CABG), aortic valve replacement (AVR) or mitral valve repair (MVR) will be randomized to either intervention or control group. The specific operation groups (CABG, AVR and MVR) will be analyzed separately. The 7-day baseline measurements of sedentary behaviour (SB), physical activity (PA) and sleep will be conducted to the patients by using the RM42 accelerometer during the pre-operative month.

After the cardiac procedure is completed and the patient is moved to post-operative ward, the control group patients will begin the standard post-operative rehabilitation program of the participating hospitals (activity guidance given by a physiotherapist). Patients in the intervention groups will follow the identical program but after discharge they will also receive personalized activity guidance through the combination of ExSed smart phone application, Suunto MoveSense accelerometer and cloud system during the first 90 days of post-operative rehabilitation. Weekly evolving daily goals to replace SB with PA (daily goals for steps, moderate PA, light PA and standing, and sitting time limit) will be designed for each patient of the intervention groups. A new daily step goal will be delivered from the cloud system to the patient's smart phone in the beginning of each week of the intervention. The daily step goal of the first intervention week is based on patient's walking distance assessed by a physiotherapist in post-operative ward. The following goals will be automatically evolved in the basis of patient's personal average step count of the previous week. The MoveSense accelerometer will measure accumulated levels of SB, PA and sleep, and transmit the data to user's ExSed application with Bluetooth. With information about accumulated levels of SB and PA, the application is able to guide the patient to accomplish the predefined activity goal. The guidance and motivation will be offered with pop-up notifications and histograms (columns are fulfilled according to patient's accumulated daily activity). The researches retain a remote access to the activity data of patients in the cloud system. The ExSed application will be connected to the cloud system with internet connection.

In addition, the patients of the intervention groups will receive short video files (lasting from 1 to 3 minutes) containing exercise guidance from a physiotherapist specialized to cardiac operation patients. These videos are available on the ExSed application during the intervention. The physiotherapist will also contact each patient (by mobile phone) with structured contact form from 1 to 4 times in a month to make sure that the intervention is proceeding as designed.

研究设计

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

入排标准

年龄范围
30 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •An eligible patient with coronary artery disease, aortic valve stenosis or mitral valve insufficiency scheduled for elective coronary artery bypass grafting, aortic valve replacement or mitral valve repair operation.
  • •He / she does not have any severe disease or functional limitation limiting PA (other than CVD).
  • •He / she is willing to wear a hip- and wrist-worn accelerometer.
  • •He / she is willing and capable to use a smart phone application.

排除标准

  • •He / she ends up in prolonged intensive care after cardiac operation.
  • •He / she has a memory disorder (i.e. Alzheimer's disease).

研究组 & 干预措施

PACO intervention for CABG patients

Experimental

The group of coronary artery disease patients receiving the PACO intervention for CABG patients besides the standard postoperative rehabilitation of Kuopio and Turku university hospitals after coronary artery bypass grafting. The PACO intervention includes activity guidance (i.e. goals to improve daily steps and physical activity levels, and reduce prolonged sitting) provided to the patients with the novel combination of ExSed application, MoveSense accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be included to the intervention.

干预措施: PACO intervention for CABG patients (Behavioral)

CABG control group

No Intervention

The group of coronary artery disease patients receiving the standard postoperative rehabilitation of Kuopio and Turku university hospitals after coronary artery bypass grafting. The post-operative rehabilitation includes written and oral physical activity guidance from a physiotherapist.

AVR control group

No Intervention

The group of aortic valve stenosis patients receiving the standard postoperative rehabilitation of Kuopio and Turku university hospitals after aortic valve replacement. The post-operative rehabilitation includes written and oral physical activity guidance from a physiotherapist.

PACO intervention for AVR patients

Experimental

The group of aortic valve stenosis patients receiving the PACO intervention for AVR patients besides the standard postoperative rehabilitation of Kuopio and Turku university hospitals after aortic valve replacement. The PACO intervention includes activity guidance (i.e. goals to improve daily steps and physical activity levels, and reduce prolonged sitting) provided to the patients with the novel combination of ExSed application, MoveSense accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be included to the intervention.

干预措施: PACO intervention for AVR patients (Behavioral)

MVR control group

No Intervention

The group of mitral valve insufficiency patients receiving the standard postoperative rehabilitation of Kuopio and Turku university hospitals after mitral valve repair. The post-operative rehabilitation includes written and oral physical activity guidance from a physiotherapist.

PACO intervention for MVR patients

Experimental

The group of mitral valve insufficiency patients receiving the PACO intervention for MVR patients besides the standard postoperative rehabilitation of Kuopio and Turku university hospitals after mitral valve repair. The PACO intervention includes activity guidance (i.e. goals to improve daily steps and physical activity levels, and reduce prolonged sitting) provided to the patients with the novel combination of ExSed application, MoveSense accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be included to the intervention.

干预措施: PACO intervention for MVR patients (Behavioral)

结局指标

主要结局

Improvement in mean daily number of steps

时间窗: Improvement between baseline (during the last preoperative month) and first 3 (and 12) months after discharge.

The improvement in mean daily number of steps after 3 months from discharge. In addition, the follow-up will be continued until 12 months after discharge. The baseline values of mean daily number of steps will be determined in a 7-day accelerometer measurements conducted to the patients before the elective cardiac operation. The mean daily number of steps after the first 3 and 12 months of post-operative rehabilitation at home will be also determined in 7-day (24 h) accelerometer measurements. The raw accelerometer data will be analyzed with Mean Amplitude Deviation and Angle for Posture Estimation -algorithms to recognize the daily steps for the 7 days of which average will be calculated for each study patient.

次要结局

  • Improvement in self-perceived quality of life (QoL) assessed with SF-36 -questionnaire(Change between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Improvement in self-perceived quality of life (QoL) assessed with SAQ-7 -questionnaire(Improvement between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Improvement in self-perceived quality of life (QoL) assessed with 15 D -questionnaire(Improvement between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Incidence of major cardiovascular events(The first 12 post-operative months)
  • Change in mean daily accumulated total time of light PA and MVPA(Change between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Change in mean daily total time of sedentary behaviour (SB)(Change between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Change in maximal oxygen consumption(Change between the first and third months after discharge.)
  • Improvement in self-perceived quality of life (QoL) assessed with PHQ-2 -questionnaire(Improvement between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Improvement in self-perceived quality of life (QoL) assessed with Rose Dyspnea Index(Improvement between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Change in the accelerometer-derived portion of deep sleep(Change between baseline (during the last preoperative month) and first 3 months after discharge.)
  • Change in heart rate variability(Change between baseline (during the last preoperative month) and first 3 months after discharge.)

研究者

发起方
Kuopio University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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