Actively Recruiting
Effectiveness of an Adapted Physical Activity Program for Subjects Suffering From Haemophilia
Led by Istituto Ortopedico Rizzoli · Updated on 2025-05-18
16
Participants Needed
1
Research Sites
63 weeks
Total Duration
On this page
Sponsors
I
Istituto Ortopedico Rizzoli
Lead Sponsor
U
University of Bologna
Collaborating Sponsor
AI-Summary
What this Trial Is About
The present study aims to evaluate the modification of functional capacity induced by an adapted physical activity program in subjects with haemophilia. The exercise program used aims to improve joint mobility, muscle strength, static and dynamic balance, motor coordination. The program is structured in 1 hour sessions of 2 days/week and lasts 6 months. The primary endpoint is the change in functional capacity calculated as the difference between the baseline assessment and the 3 and 6 month assessment of the 6 Minutes Walking Test measured with the G-Walk (BTS Bioengineering S.p.A).
CONDITIONS
Official Title
Effectiveness of an Adapted Physical Activity Program for Subjects Suffering From Haemophilia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hemophilia A or B
- Signature of informed consent
- Availability of a medical certificate for non-competitive activities
You will not qualify if you...
- Active bleeding
- Severe joint deformities that prevent exercise
- Severe communicative or sensory impairments that prevent understanding or following instructions (such as dementia, aphasia, blindness, deafness)
- Heart failure with NYHA class greater than 2
- Unstable angina
- Lung disease requiring oxygen therapy
- Symptomatic peripheral arterial disease
- Myocardial infarction or hospitalization within the previous 6 months
- Symptomatic orthostatic hypotension
- Hypertension not well controlled with medication (diastolic > 95 mmHg, systolic > 160 mmHg)
- Significant neurological conditions affecting motor or cognitive functions
AI-Screening
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Trial Site Locations
Total: 1 location
1
Istituto Ortopedico Rizzoli
Bologna, Bo, Italy, 40130
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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