CopenHeart IE - Integrated Rehabilitation of Patients Treated for Infective Endocarditis
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About
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.
Full 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.
Enrollment
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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
Trial design
Primary purpose
Allocation
Interventional model
Masking
117 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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