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Personalized Activity Intervention in Rehabilitation After Cardiac Operations (the PACO Trial) (PACO)

Primary Purpose

Coronary Artery Disease, Aortic Valve Stenosis, Mitral Valve Insufficiency

Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
PACO intervention for CABG patients
PACO intervention for AVR patients
PACO intervention for MVR patients
Sponsored by
Kuopio University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Coronary Artery Disease focused on measuring Accelerometer, Aortic valve replacement, Aortic valve stenosis, Coronary artery bypass grafting, Coronary artery disease, eHealth, Interactive guidance, Mitral valve insufficiency, Mitral valve repair, Rehabilitation

Eligibility Criteria

30 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

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

Sites / Locations

  • Kuopio University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

No Intervention

Experimental

No Intervention

Experimental

No Intervention

Experimental

Arm Label

CABG control group

PACO intervention for CABG patients

AVR control group

PACO intervention for AVR patients

MVR control group

PACO intervention for MVR patients

Arm Description

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.

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.

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.

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.

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.

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.

Outcomes

Primary Outcome Measures

Improvement in mean daily number of steps
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.

Secondary Outcome Measures

Change in mean daily accumulated total time of light PA and MVPA
The post-operative change in patient's mean daily accumulated total time of light and moderate to vigorous physical activity.
Change in mean daily total time of sedentary behaviour (SB)
The post-operative change in patient's mean daily total time of SB.
Change in maximal oxygen consumption
The evolvement of patient's maximal oxygen consumption (VO2 peak) will be determined in 6 minute walking test, conducted to the patients twice (after 1 and 3 months) post-operatively. Only a part of the randomized patients coming from city areas of Kuopio and Turku will be included to the measurements of maximal oxygen consumption.
Improvement in self-perceived quality of life (QoL) assessed with SAQ-7 -questionnaire
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with Seattle Angina Questionnaire 7 (SAQ-7).
Improvement in self-perceived quality of life (QoL) assessed with SF-36 -questionnaire
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with SF-36 -questionnaire.
Improvement in self-perceived quality of life (QoL) assessed with 15 D -questionnaire
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with 15 D -questionnaire.
Improvement in self-perceived quality of life (QoL) assessed with PHQ-2 -questionnaire
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with PHQ-2 -questionnaire.
Improvement in self-perceived quality of life (QoL) assessed with Rose Dyspnea Index
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with Rose Dyspnea Index.
Incidence of major cardiovascular events
The major cardiovascular events include: all-cause mortality, any rehospitalizations due to CVD, repeat coronary revascularization, non-operational myocardial infarction and stroke. The incidence of major cardiovascular events will be monitored from the patient records of the hospitals and HILMO database during the first 12 post-operative months. In addition, patients will be asked about cardiovascular events during research telephone contact (after 12 months of rehabilitation).
Change in the accelerometer-derived portion of deep sleep
The change in patient's deep sleep portion after cardiac operations. Deep sleep will be recognized with accelerometer attached to patient's wrist during sleep. Accelerometer will be used during 7 days.
Change in heart rate variability
The change in the heart rate variability.

Full Information

First Posted
February 28, 2018
Last Updated
August 14, 2019
Sponsor
Kuopio University Hospital
Collaborators
UKK Institute, Turku University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03470246
Brief Title
Personalized Activity Intervention in Rehabilitation After Cardiac Operations (the PACO Trial)
Acronym
PACO
Official Title
Personalized Intervention to Increase Physical Activity and Reduce Sedentary Behaviour in Rehabilitation After Cardiac Operations (the PACO Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Recruiting
Study Start Date
April 6, 2018 (Actual)
Primary Completion Date
January 2022 (Anticipated)
Study Completion Date
March 1, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kuopio University Hospital
Collaborators
UKK Institute, Turku University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Aortic Valve Stenosis, Mitral Valve Insufficiency
Keywords
Accelerometer, Aortic valve replacement, Aortic valve stenosis, Coronary artery bypass grafting, Coronary artery disease, eHealth, Interactive guidance, Mitral valve insufficiency, Mitral valve repair, Rehabilitation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The PACO trial is based on randomized clinical trial. Besides the standard post-operative care, the cardiac operation patients of the intervention groups will receive activity guidance during a 90-day intervention after elective coronary artery bypass grafting, aortic valve replacement or mitral valve repair. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be provided to the intervention patients.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
540 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CABG control group
Arm Type
No Intervention
Arm Description
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.
Arm Title
PACO intervention for CABG patients
Arm Type
Experimental
Arm Description
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.
Arm Title
AVR control group
Arm Type
No Intervention
Arm Description
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.
Arm Title
PACO intervention for AVR patients
Arm Type
Experimental
Arm Description
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.
Arm Title
MVR control group
Arm Type
No Intervention
Arm Description
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.
Arm Title
PACO intervention for MVR patients
Arm Type
Experimental
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
PACO intervention for CABG patients
Intervention Description
The PACO intervention is based on post-operative guidance to replace prolonged SB with PA in the rehabilitation of patients recovering from coronary artery bypass grafting (CABG). The guidance will be provided to the patients with the combination of ExSed smart phone application, accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be provided to the intervention patients.
Intervention Type
Behavioral
Intervention Name(s)
PACO intervention for AVR patients
Intervention Description
The PACO intervention is based on post-operative guidance to replace prolonged SB with PA in the rehabilitation of patients recovering from aortic valve replacement (AVR). The guidance will be provided to the patients with the combination of ExSed smart phone application, accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be provided to the intervention patients.
Intervention Type
Behavioral
Intervention Name(s)
PACO intervention for MVR patients
Intervention Description
The PACO intervention is based on post-operative guidance to replace prolonged SB with PA in the rehabilitation of patients recovering from mitral valve repair (MVR). The guidance will be provided to the patients with the combination of ExSed smart phone application, accelerometer and cloud system. In addition, exercise guidance (short video files) and regular mobile phone contacts from physiotherapist will be provided to the intervention patients.
Primary Outcome Measure Information:
Title
Improvement in mean daily number of steps
Description
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.
Time Frame
Improvement between baseline (during the last preoperative month) and first 3 (and 12) months after discharge.
Secondary Outcome Measure Information:
Title
Change in mean daily accumulated total time of light PA and MVPA
Description
The post-operative change in patient's mean daily accumulated total time of light and moderate to vigorous physical activity.
Time Frame
Change between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Change in mean daily total time of sedentary behaviour (SB)
Description
The post-operative change in patient's mean daily total time of SB.
Time Frame
Change between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Change in maximal oxygen consumption
Description
The evolvement of patient's maximal oxygen consumption (VO2 peak) will be determined in 6 minute walking test, conducted to the patients twice (after 1 and 3 months) post-operatively. Only a part of the randomized patients coming from city areas of Kuopio and Turku will be included to the measurements of maximal oxygen consumption.
Time Frame
Change between the first and third months after discharge.
Title
Improvement in self-perceived quality of life (QoL) assessed with SAQ-7 -questionnaire
Description
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with Seattle Angina Questionnaire 7 (SAQ-7).
Time Frame
Improvement between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Improvement in self-perceived quality of life (QoL) assessed with SF-36 -questionnaire
Description
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with SF-36 -questionnaire.
Time Frame
Change between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Improvement in self-perceived quality of life (QoL) assessed with 15 D -questionnaire
Description
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with 15 D -questionnaire.
Time Frame
Improvement between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Improvement in self-perceived quality of life (QoL) assessed with PHQ-2 -questionnaire
Description
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with PHQ-2 -questionnaire.
Time Frame
Improvement between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Improvement in self-perceived quality of life (QoL) assessed with Rose Dyspnea Index
Description
The improvement in patient's post-operative quality of life after 3 months of rehabilitation. The quality of life will be determined with Rose Dyspnea Index.
Time Frame
Improvement between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Incidence of major cardiovascular events
Description
The major cardiovascular events include: all-cause mortality, any rehospitalizations due to CVD, repeat coronary revascularization, non-operational myocardial infarction and stroke. The incidence of major cardiovascular events will be monitored from the patient records of the hospitals and HILMO database during the first 12 post-operative months. In addition, patients will be asked about cardiovascular events during research telephone contact (after 12 months of rehabilitation).
Time Frame
The first 12 post-operative months
Title
Change in the accelerometer-derived portion of deep sleep
Description
The change in patient's deep sleep portion after cardiac operations. Deep sleep will be recognized with accelerometer attached to patient's wrist during sleep. Accelerometer will be used during 7 days.
Time Frame
Change between baseline (during the last preoperative month) and first 3 months after discharge.
Title
Change in heart rate variability
Description
The change in the heart rate variability.
Time Frame
Change between baseline (during the last preoperative month) and first 3 months after discharge.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: He / she ends up in prolonged intensive care after cardiac operation. He / she has a memory disorder (i.e. Alzheimer's disease).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ville Vasankari, B.M. with thesis
Phone
505208148
Ext
+358
Email
villevas@uef.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Jari Halonen, M.D.; Ph.D.
Phone
405885829
Ext
+358
Email
jari.halonen@kuh.fi
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jari Halonen, M.D.; Ph.D.
Organizational Affiliation
Heart Center, Kuopio University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kuopio University Hospital
City
Kuopio
ZIP/Postal Code
70029
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jari Halonen, M.D., Ph.D.
Phone
405885829
Ext
+358
Email
jari.halonen@kuh.fi

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35842711
Citation
Vasankari S, Hartikainen J, Vasankari V, Anttila V, Tokola K, Vaha-Ypya H, Husu P, Sievanen H, Vasankari T, Halonen J. Objectively measured preoperative physical activity and sedentary behaviour among Finnish patients scheduled for elective cardiac procedures: baseline results from randomized controlled trial. BMC Sports Sci Med Rehabil. 2022 Jul 16;14(1):130. doi: 10.1186/s13102-022-00522-1.
Results Reference
derived
PubMed Identifier
33962483
Citation
Abraham LN, Sibilitz KL, Berg SK, Tang LH, Risom SS, Lindschou J, Taylor RS, Borregaard B, Zwisler AD. Exercise-based cardiac rehabilitation for adults after heart valve surgery. Cochrane Database Syst Rev. 2021 May 7;5(5):CD010876. doi: 10.1002/14651858.CD010876.pub3.
Results Reference
derived
PubMed Identifier
31354960
Citation
Vasankari V, Halonen J, Husu P, Vaha-Ypya H, Tokola K, Suni J, Sievanen H, Anttila V, Airaksinen J, Vasankari T, Hartikainen J. Personalised eHealth intervention to increase physical activity and reduce sedentary behaviour in rehabilitation after cardiac operations: study protocol for the PACO randomised controlled trial (NCT03470246). BMJ Open Sport Exerc Med. 2019 Jul 5;5(1):e000539. doi: 10.1136/bmjsem-2019-000539. eCollection 2019.
Results Reference
derived

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Personalized Activity Intervention in Rehabilitation After Cardiac Operations (the PACO Trial)

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