- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01912248
Acute Effect of Strength Training on Blood Pressure in Cardiac Patients
January 26, 2015 updated by: Christian Dall
Moderate and heavy strength training exercise and the acute blood pressure rise in cardiac patient, how high?
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
12 heart transplant recipients 12 heart failure patients 12 patients with ischemic heart disease
Study Type
Observational
Enrollment (Actual)
36
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Copenhagen, Denmark, 2400
- Christian Dall
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
12 heart transplant recipients 12 heart failure patients 12 patients with ischemic disease
Description
Inclusion Criteria:
- 18 years
- no strength training > 3 month
- speak and understand danish
Exclusion Criteria:
- cancer
- serum creatinin above 200 mmol/l
- re-transplantation
- Ejection fraction > 35
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Heart failure
strength training
|
strength training, lower limb.
Other Names:
|
Heart Transplant recipients
strength training
|
strength training, lower limb.
Other Names:
|
patients with ischemic heart disease
strength training
|
strength training, lower limb.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
systolic blood pressure
Time Frame: one test, 1 hour, continuated systolic blood pressure surveliance
|
one test, 1 hour, continuated systolic blood pressure surveliance
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
diastolic blood pressure
Time Frame: one test 1 hour, continuated bloodpressure surveliance
|
one test 1 hour, continuated bloodpressure surveliance
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Christian H Dall, cand.scient, Bispebjerg Hospital, Denmark
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2013
Primary Completion (Actual)
April 1, 2014
Study Completion (Actual)
April 1, 2014
Study Registration Dates
First Submitted
July 29, 2013
First Submitted That Met QC Criteria
July 30, 2013
First Posted (Estimate)
July 31, 2013
Study Record Updates
Last Update Posted (Estimate)
January 27, 2015
Last Update Submitted That Met QC Criteria
January 26, 2015
Last Verified
January 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-2-2012-143
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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