Bilateral Deficit Phenomenon in Patients With Haemophilic Arthropathy

NCT ID: NCT02165462

Last Updated: 2016-07-28

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

17 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-09-30

Study Completion Date

2015-10-31

Brief Summary

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Trial to assess the bilateral deficit phenomenon during dynamic plantar flexion task in patients with haemophilic arthropathy Describe the differences in terms of the physical variables (muscular strength, range of motion and proprioception) in patients with hemophilia who have conducted a home treatment with a digital tool.

Bookmark the relationship between clinical history of joint bleeds and clinical manifestations in standing and walking.

Detailed Description

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* Assess the bilateral deficit phenomenon during dynamic plantar flexion task in patients with haemophilic arthropathy.
* Indicate the independent variables that influence the development of strength and contractile activity, with or without previous joint bleeds in haemophilia patients with minors.
* Observe the descriptive variables people influence the standing, the incorporation from sitting and jumping.

Conditions

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Hemophilia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with haemophilia

Assessment of bilateral deficit phenomenon during dynamic plantar flexion task

Patients with haemophilia

Intervention Type OTHER

Assessment of bilateral deficit phenomenon during dynamic plantar flexion task with a force platform (Kistler 9286 BA model, Kistler Instruments, Amherst, NY, USA)

Interventions

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Patients with haemophilia

Assessment of bilateral deficit phenomenon during dynamic plantar flexion task with a force platform (Kistler 9286 BA model, Kistler Instruments, Amherst, NY, USA)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed with hemophilia A and B.
* With or without joint involvement clinically diagnosed, and with or without a previous history of hemarthrosis joint load legs.
* In prophylactic regimen with FVIII / FIX concentrates .
* Residents in the Autonomous Community of the Region of Murcia.

Exclusion Criteria

* Patients without walking ability.
* Patients diagnosed with other congenital coagulopathy (von Willebrand disease, etc..).
* Patients with neurological or cognitive impairments that prevent understanding the questionnaires and physical tests.
* Patients whose parents or guardians have not signed the informed consent document.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Universidad Católica San Antonio de Murcia

OTHER

Sponsor Role lead

Responsible Party

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Rubén Cuesta-Barriuso, PhD

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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JUAN JOSE RODRIGUEZ, MsC

Role: STUDY_CHAIR

Universidad Católica San Antonio

RUBEN CUESTA-BARRIUSO, PhD

Role: PRINCIPAL_INVESTIGATOR

Universidad Católica San Antonio

Locations

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Universidad Católica San Antonio, Murcia

Murcia, Murcia, Spain

Site Status

Countries

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Spain

Other Identifiers

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PROPRIO-HE

Identifier Type: -

Identifier Source: org_study_id

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