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

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

      • Copenhagen, Denmark, 2400
        • Christian Dall

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:
  • one hour of strength training.
Heart Transplant recipients
strength training
strength training, lower limb.
Other Names:
  • one hour of strength training.
patients with ischemic heart disease
strength training
strength training, lower limb.
Other Names:
  • one hour of strength training.

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

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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