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Assessment of Proprioceptive and Functional Characteristics in Patients With Hemophilia (HE-BALANCE)

U

Universidad Católica San Antonio de Murcia

Status

Unknown

Conditions

Hemophilia

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Analyze and evaluate the skeletal muscle of patients affected with hemophilia in the Region of Murcia.

  • Describe the periarticular muscular deficit of the lower limbs, depending on the degree of injury: acute and chronic, or subacute.
  • Identify the range of motion of joints with higher prevalence of hemophilic arthropathy.
  • Detect the biomechanical changes of the lower limbs and their impact on gait in patients with hemophilia.
  • Assess the factors that influence the perception of illness and quality of life of patients with hemophilia.

Full description

Descriptive study of joint involvement in hemophilia patients with and without a history of hemarthrosis in lower limbs.

Descriptive study of alterations in the strength of the periarticular muscles of lower limbs as a result of acute conditions or the development of chronic articular sequelae.

Descriptive study of the biomechanical alterations in weight-bearing joints of lower limbs and their impact on gait in patients with hemophilia.

Descriptive study of the relationship between skeletal muscle pathology in patients with hemophilia and their perceptions of it and their quality of life.

Enrollment

60 estimated patients

Sex

Male

Ages

6 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with hemophilia A and B
  • Patients of all ages (from 6 to 70 years).
  • With or without joint damage clinically diagnosed, and with or without a previous history of hemarthrosis joint load legs.
  • Residents in the Autonomous Community of the Region of Murcia.

Exclusion criteria

  • Patients without ambulation
  • Patients diagnosed with other congenital coagulopathy (von Willebrand disease, etc..).
  • Patients with neurological or cognitive impairments that prevent understanding the questionnaires and physical tests.

Trial design

60 participants in 1 patient group

Patients with hemophilia
Description:
Patients with hemophilia who meet the inclusion criteria

Trial contacts and locations

1

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Central trial contact

RUBÉN CUESTA-BARRIUSO, PhD

Data sourced from clinicaltrials.gov

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