Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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9 January 2017 |
Main ID: |
NCT02290262 |
Date of registration:
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07/11/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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SheppHeartCABG - Phase One Rehabilitation After Coronary Artery Bypass Grafting
SheppHeart |
Scientific title:
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SheppheartCABG. A Randomised Clinical Trial of a Comprehensive Physical and Psycho-educative Rehabilitation Programme Plus Usual Care Versus Usual Care in Phase 1 Rehabilitation After Coronary Artery Bypass Grafting |
Date of first enrolment:
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November 2014 |
Target sample size:
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326 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02290262 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research
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Phase:
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N/A
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Countries of recruitment
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Denmark
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Contacts
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Name:
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Selina Berg, PhD |
Address:
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Telephone:
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Email:
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Affiliation:
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Rigshospitalet, Denmark |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients 18 years or older with ischaemic heart disease,
- Who have to undergo elective coronary artery bypass grafting,
- Who speak and understand Danish and
- Who provide a written informed consent will be included.
Exclusion Criteria:
Patients will be excluded from the trial:
- Patients at intermediate or high risk to their cardiovascular status according to
guidelines,
- Patients with neurological or orthopaedic deficits which prevent training and
- Patients who do not wish to participate.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Ischaemic Heart Disease
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Intervention(s)
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Other: Comprehensive phase one rehabilitation
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Primary Outcome(s)
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6-minute walk test
[Time Frame: 4 week]
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Secondary Outcome(s)
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Composite secondary outcomes
[Time Frame: 4 week]
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Secondary ID(s)
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SheppHeartCABG RCT
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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