This study evaluates the clinical impact of a progressive resistance training program in
adults patients with haemophilia
Other: Progressive resistance training
Other: Normal daily activities
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Locations near you
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Full eligibility criteria for NCT02781233
Ages eligible for Study
18 Years to 60 Years
Genders eligible for Study
Accepts Healthy Volunteers
diagnosis of haemophilia A or B
willingness to exercise twice a week during the training program and to complete the pre- and post-program evaluations
approval by their hematologist to participate in the exercise program
age between 18 and 60 years
informed consent signed.
the inability to attend exercise sessions at least twice a week for 6 consecutive weeks
non adherence to instruction on proper exercise technique
surgical procedures performed 6 weeks prior to or during the exercise program
participation in any other form of exercise, including rehabilitation, during the study; (5) changes in medication during the study
a major bleeding episode that posed a risk or prevented exercise
History of FVIII inhibitor (titer ≥ 0.6 BU [Bethesda unit]) or detectable FVIII inhibitors at screening (titer ≥ 0.4 BU)
Another haemostatic defect
Need for major surgery
Withdrawal of informed consent
All locations for NCT02781233
University of Valencia
Valencia, Spain, 46010
not yet recruiting
View full eligibility
Tris trial is registered with FDA with number: NCT02781233. The sponsor of the trial is University of Valencia and it is looking for 35 volunteers for the current phase.
Official trial title: The Impact of Progressive Resistance Training on Quality of Life in Patients With Haemophilia
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