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Clinical Trials/NCT01935297
NCT01935297
Completed
N/A

Safety, Applicability and Outcome of Regular Exercise Training After Transcatheter Aortic Valve Implantation

Technical University of Munich1 site in 1 country30 target enrollmentJune 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Transcatheter Aortic Valve Replacement
Sponsor
Technical University of Munich
Enrollment
30
Locations
1
Primary Endpoint
Change of peak oxygen uptake
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This pilot study will evaluate the effect of a rehabilitative exercise training on exercise capacity in patients after percutaneous aortic valve replacement. It will additionally evaluate the safety of such an approach and the effect on life quality. We hypothesize that regular structured exercise improves exercise capacity in these patients beyond the sole effect of the valve procedure.

Detailed Description

The study will include 30 patients and randomize them in a 1:1-fashion to either a training or a usual care group. The training group will undergo 8 weeks of combined endurance and resistance training according to a standard protocol, but with individual adjustment if required. The usual care group will receive general advice but no structured exercise program. Exercise capacity is assessed by cardiopulmonary exercise testing and by the 6 minute walk test prior to and after the intervention period. In addition, life quality will be assessed by validated questionnaires, while safety will be assessed by recording adverse events and by echocardiography.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
January 2015
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Technical University of Munich
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients up to 6 months after transcatheter aortic valve implantation

Exclusion Criteria

  • inability to perform exercise on bicycles valve dysfunction

Outcomes

Primary Outcomes

Change of peak oxygen uptake

Time Frame: Baseline to 8 weeks

Secondary Outcomes

  • Change of quality of life(Baseline to 8 weeks)

Study Sites (1)

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