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CopenHeart IE - Integrated Rehabilitation of Patients Treated for Infective Endocarditis

Primary Purpose

Infective Endocarditis

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Complex Cardiac rehabilitation
Control group
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Infective Endocarditis focused on measuring Rehabilitation, Exercise training, Psycho-educational care

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients:

  • treated for leftsided- (native- or prosthetic valve) or cardiac device endocarditis based on Duke Criteria
  • 18 years or older
  • speaking and understanding Danish
  • providing written informed consent

Exclusion Criteria:

Patients:

  • unable to understand study instructions
  • with an ischemic event within the past 6 months
  • who are pregnant or breastfeeding
  • with reduced ability to follow the planned programme due to i.e. substance abuse problems or other somatic illness
  • with considerable illness in the musculoskeletal system or with physical disability, which complicates exercise training
  • whose physician advise against participation

Sites / Locations

  • Rigshospitalet / gentofte hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Intervention group

Control group

Arm Description

Complex Cardiac Rehabilitation

Usual care

Outcomes

Primary Outcome Measures

Change in Mental component scale
Measured by the mental component scale (MCS) in the SF-36 questionnaire

Secondary Outcome Measures

Change in physical capacity
Measured by Peak VO2 via ergospirometry testing

Full Information

First Posted
January 11, 2012
Last Updated
September 10, 2019
Sponsor
Rigshospitalet, Denmark
Collaborators
University Hospital, Gentofte, Copenhagen, Copenhagen Trial Unit, Center for Clinical Intervention Research
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1. Study Identification

Unique Protocol Identification Number
NCT01512615
Brief Title
CopenHeart IE - Integrated Rehabilitation of Patients Treated for Infective Endocarditis
Official Title
CopenHeart IE - A Randomized Clinical Trial Investigating the Effect and Meaning of Integrated Rehabilitation Versus Usual Follow-up of Patients Treated for Infective Endocarditis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
December 2011 (Actual)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
University Hospital, Gentofte, Copenhagen, Copenhagen Trial Unit, Center for Clinical Intervention Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to describe the effect and meaning of an integrated rehabilitation programme, consisting of physical training and psycho-educational care, for patients treated for infective endocarditis. The hypothesis is, that integrated rehabilitation can improve mental health, physical capacity and other factors.
Detailed Description
Infective endocarditis (IE) is among the most serious infectious diseases in the western world. Treatment requires lengthy hospitalization, high dosage antibiotics and possible valve replacement surgery. Studies indicate that patients experience persisting physical symptoms, diminished quality of life and difficulties returning to work, up to a year post-discharge. No studies investigating the effect of, interventions aimed at relieving these problems, have been published. A randomized clinical trial is conducted to investigate the effect and meaning of an integrated rehabilitation programme on the physical and psychosocial functioning of patients treated for IE. The trial is a multi-centre, parallel arm design. A mixed methods embedded experimental design is chosen to include both quantitative and qualitative data to evaluate the intervention. The intervention consists of five psycho-educational consultations provided by specialized nurses and a twelve week individualized exercise training programme provided by physiotherapists. A qualitative and a survey-based pre-study will be undertaken, to investigate post-discharge experiences and rehabilitation needs of patients treated for IE. A qualitative post-intervention study will explore rehabilitation participation experiences. The hypothesis is, that integrated rehabilitation can improve mental health, physical capacity, self-rated health, quality of life, nutritional status, sleep-quality and body-image and reduce anxiety, depression, fatigue, health care utilisation, work cessation and mortality in patients treated for IE and that it is cost effective. 150 patients treated for leftsided- (native- or prosthetic valve) or cardiac device endocarditis will be included in the trial Questionnaires, cardiopulmonary testing, 6 minute walking test and qualitative interviews will be used to evaluate the effect and meaning of the programme.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infective Endocarditis
Keywords
Rehabilitation, Exercise training, Psycho-educational care

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
RCT
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
117 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Complex Cardiac Rehabilitation
Arm Title
Control group
Arm Type
Experimental
Arm Description
Usual care
Intervention Type
Other
Intervention Name(s)
Complex Cardiac rehabilitation
Intervention Description
Complex Cardiac Rehabilitation consisting of exercise training (minimum 3 times a week for a total of twelve weeks) and psychoeducational care (5 sessions over 6 months)
Intervention Type
Other
Intervention Name(s)
Control group
Intervention Description
Usual care, clinical control as provided by treating heart centre
Primary Outcome Measure Information:
Title
Change in Mental component scale
Description
Measured by the mental component scale (MCS) in the SF-36 questionnaire
Time Frame
1, 4, 6 and 12 months
Secondary Outcome Measure Information:
Title
Change in physical capacity
Description
Measured by Peak VO2 via ergospirometry testing
Time Frame
1, 4 and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients: treated for leftsided- (native- or prosthetic valve) or cardiac device endocarditis based on Duke Criteria 18 years or older speaking and understanding Danish providing written informed consent Exclusion Criteria: Patients: unable to understand study instructions with an ischemic event within the past 6 months who are pregnant or breastfeeding with reduced ability to follow the planned programme due to i.e. substance abuse problems or other somatic illness with considerable illness in the musculoskeletal system or with physical disability, which complicates exercise training whose physician advise against participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Trine B Rasmussen, PhD fellow
Organizational Affiliation
Copenhagen University Hospital Rigshospitalet, University Hospital Gentofte
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Selina K Berg, MScN, Ph.d.
Organizational Affiliation
Copenhagen University Hospital Rigshospitalet, University Hospital Gentofte
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ann-Dorthe Zwisler, MD, Ph.d.
Organizational Affiliation
Copenhagen University Hospital Rigshospitalet, National Institute of Public Health, University of Southern Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Henning Bundgaard, MD, Ph.d.
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philip Moons, Prof, PhD
Organizational Affiliation
Centre for Health Services and Nursing Research, KU Leuven-University of
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet / gentofte hospital
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
34089600
Citation
Rasmussen TB, Zwisler AD, Risom SS, Sibilitz KL, Christensen J, Bundgaard H, Moons P, Thygesen LC, Lindschou J, Norekval TM, Berg SK. Comprehensive cardiac rehabilitation for patients following infective endocarditis: results of the randomized CopenHeartIE trial. Eur J Cardiovasc Nurs. 2022 Apr 9;21(3):261-270. doi: 10.1093/eurjcn/zvab047.
Results Reference
derived
PubMed Identifier
24704921
Citation
Rasmussen TB, Zwisler AD, Moons P, Berg SK. Insufficient living: experiences of recovery after infective endocarditis. J Cardiovasc Nurs. 2015 May-Jun;30(3):E11-9. doi: 10.1097/JCN.0000000000000144.
Results Reference
derived
PubMed Identifier
23175738
Citation
Rasmussen TB, Zwisler AD, Sibilitz KL, Risom SS, Bundgaard H, Gluud C, Moons P, Winkel P, Thygesen LC, Hansen JL, Norekval TM, Berg SK; CopenHeartIE Group. A randomised clinical trial of comprehensive cardiac rehabilitation versus usual care for patients treated for infective endocarditis--the CopenHeartIE trial protocol. BMJ Open. 2012 Nov 21;2(6):e001929. doi: 10.1136/bmjopen-2012-001929. Print 2012.
Results Reference
derived

Learn more about this trial

CopenHeart IE - Integrated Rehabilitation of Patients Treated for Infective Endocarditis

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