Educational Physiotherapy in Haemophilia

Not Applicable

Completed

• Conditions: Haemophilia
• Interventions: Other: Educational physiotherapy group

• Registration Number: NCT02825706
• Lead Sponsor: Real Fundación Victoria Eugenia

Brief Summary

Although arthropathy is a serious problem in patients with hemophilia due to the associated morbidity and incapacity, to the best of the investigators knowledge, no studies have looked at the effect of educational physiotherapy for its clinical improvement.

This contribution presents the results of educational physiotherapy program applied for 15 weeks with home exercises - in patients with hemophilic arthropathy. After treatment, experimental group showed improved a significant reduction of pain, and best quality of life al illness behaviour. During treatment no patient showed elbow haemarthrosis, which underlines the safety of this physiotherapy program.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-02
• Primary Completion: 2012-10
• Study Completion: 2015-04
• Study First Submitted: 2016-06-30
• Status Verified: 2016-07
• Study First Submitted QC: 2016-07-06
• Last Update Submitted: 2016-07-06
• Study First Posted: 2016-07-07
• Last Update Posted: 2016-07-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 20

Inclusion Criteria

• Patients diagnosed with hemophilia A or B
• Patients over 18 years
• Patients with hemophilic arthropathy with at least 1 involved joint (elbow, knee or ankle)
• having signed the informed consent document.

Exclusion Criteria

• Patients diagnosed with other congenital bleeding disorders (i.e. von Willebrand disease)
• Patients who developed antibodies to FVIII or FIX (inhibitors)
• Those not able to ambulate as a result of hemophilic arthropathy or any other disability

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Experimental group	Educational physiotherapy group	The patients in experimental group received 60-minute educational sessions every two weeks about the pathophysiology of hemophilia, clinical manifestations, postural advice and prevention advice to avoid recurrent bleeding. Likewise, doubts on the clinical progress of hemophilic arthropathy, functional limitations and management of joint pain were resolved. In parallel with the educational sessions, patients followed a 15-week home exercise program performed once a day, 6 days a week. The program included muscle stretching exercises; isometric exercises; proprioceptive exercises on one leg with visual support; and a 20-minute walk. Low-intensity exercises with 20-25 repetitions were included.

Primary Outcome Measures

Name	Time	Method
Change from baseline physical condition of joints after treatment and at 6 months	Screening visit, within the first seven days after treatment and after six months follow-up visit	The physical condition of joints was assessed using the Gilbert scale that measures swelling, muscle atrophy, joint crepitus, range of motion, axial deformity and instability. Scores range from 0 to 12 (0 represents no joint injury and 12 represents maximum joint deterioration).
Change from baseline joint pain after treatment and at 6 months	Screening visit, within the first seven days after treatment and after six months follow-up visit	Joint pain was assessed using the Visual Analog Scale (VAS), with scores ranging from 0 (no pain at all) to 10 (the worst pain imaginable by the patient).
Change from baseline perception of the quality of life after treatment and at 6 months	Screening visit, within the first seven days after treatment and after six months follow-up visit	The Haemophilia A-36 questionnaire was used to assess the perception of the quality of life. This questionnaire consists of 36 items that assess 9 domains (physical health, daily activities, joint damage and pain, treatment satisfaction, treatment difficulties, emotional functioning, mental health and social relationships).
Change from baseline illness behavior after treatment and at 6 months	Screening visit, within the first seven days after treatment and after six months follow-up visit	To assess illness behavior, patients completed the Illness Behavior Questionnaire (IBQ). This scale consists of 62 items and 8 domains (hypochondriasis, disease conviction, psychological vs. somatic perception of illness, affective inhibition, affective disturbance, denial and irritability).
Change from baseline frequency of bleedings after treatment and at 6 months	Screening visit, within the first seven days after treatment and after six months follow-up visit	The frequency of bleeding is measured with a record which complete the patients, where they indicate the incidence of hematomas and hemarthrosis during the treatment and follow-up.

Secondary Outcome Measures

Name	Time	Method
Radiological joint deterioration	Screening visit	All patients had an assessment of radiological joint deterioration using the Pettersson scale. This scale, with scores ranging from 0 (a normal joint) to 13 (maximum joint deterioration), is the most widely used to assess joint degeneration produced by hemophilic arthropathy. The evaluation of radiological joint damage was done at the beginning of the study.
Age	Screening visit	Age of patients included in the study
Weight	Screening visit	Weight of the patients
Height	Screening visit	Height of patients