Exploratory Pilot Study of Physical Activity Monitoring in Adult Patients With Haemophilia A by Means of Accelerometry

Hemophilia A, Congenital Clinical Trial

Official title:

Descriptive Pilot Study of Monitoring of Physical Activity in Adult Patients With Haemophilia A Arthropathy by Means of Accelerometry, Image Tests and Physical Condition Parameters. Benefits Associated With That Monitoring"

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02253693
• Other study ID #: H14-23641
• Status: Completed
• Phase: N/A
• First received: September 22, 2014
• Last updated: January 8, 2018
• Start date: January 2015
• Est. completion date: January 2017

Study information

• Verified date: January 2018
• Source: University of Valencia
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Research Question: Does an specific and pre-defined physical exercise prescribed by a specialist provide any benefit on haemophilic arthropathy, the quality of life or the physical condition of patients with haemophilia A and haemophilic arthropathy? Does adherence to physical exercise improve when monitoring patients with an accelerometer? Do compliant patients find higher benefit on haemophilic arthropathy, quality of life or the physical condition than non-compliant patients?

Primary Endpoint: Assess in patients with haemophilia A and haemophilic arthropathy if a prescribed and specific physical exercise monitored by an accelerometer is producing any change in the following domains: progress of haemophilic arthropathy; health-related quality of life; physical condition.

Secondary Endpoints: Evaluate the adherence to physical exercise in patients with haemophilia A and haemophilic arthropathy by means of accelerometry, and asses if compliant patients achieve higher improvement in these 3 domains than non-complaint patients.

Description:

Specific details of Treatment/Intervention:

Physical exercises that are part of the specific medical program prescribed for each patient. The exercise program for each patient will depend of the haemophilic arthropathy, the level of physical condition and the preferences of the patient.

Monitoring of physical activity will be made by means of accelerometers. Its use does not alter the daily activities and does not require any change of the patients' individual habits. The assessment of the patients' cardiovascular condition will be made using pulse monitors. Normal examinations in clinical practice will be revised as well as those specific to each patient reference health centre, muscle strength and joint use testing which will be validated with force measurement devices. Assess by means of an ultrasound system the baseline situation of the joints used for daily activities for injury control. Determine the likelihood of fracture and assess the bone quality by means of densitometry. Thermal cameras will allow to analyse the characteristics of Joint inflammation. It may be suitable for bleeding evolution control. Measurements given by densitometers will allows to determine the state of bones of the participants in the study (osteoporosis measurement). Number of bleeding events/hemarthrosis during the period of study. Determine the activity of hemarthros/synovitis using thermal images.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: January 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Male patients over 18

• Patients diagnosed with haemophilia A and under prophylaxis treatment with the same FVIII for 2 years prior to the inclusion in the study.

• Patients with haemophilic arthropathy in, at least, one of the four load-bearing joints (knees and ankles), according to clinical and/or radiographic criteria (at least 3 in the Gilbert scale and /or at least 3 in the Pettersson scale) and/or Chronic synovitis evidenced by ultrasound.

• Patients with signed informed consent.

Exclusion Criteria:

• Patients who have developed an inhibitor antibody (=5 Bethesda units), at the moment of the inclusion in the study.

• Development of inhibitors

• Modification, during follow-up, of FVIII with which the patient started the study.

• The patient decides to withdraw voluntarily from the study.

• Major orthopaedic surgery

Related Conditions & MeSH terms

• Hemophilia A
• Hemophilia A, Congenital

Locations

Country	Name	City	State
Spain	Hospital Universitari i Politècnic La Fe de Valencia	Valencia
Spain	University of Valencia	Valencia

Sponsors (2)

Lead Sponsor	Collaborator
University of Valencia	Baxter Healthcare Corporation

Country where clinical trial is conducted

Spain, 

References & Publications (3)

González LM, Peiró-Velert C, Devís-Devís J, Valencia-Peris A, Pérez-Gimeno E, Pérez-Alenda S, Querol F. Comparison of physical activity and sedentary behaviours between young haemophilia A patients and healthy adolescents. Haemophilia. 2011 Jul;17(4):676-82. doi: 10.1111/j.1365-2516.2010.02469.x. Epub 2011 Feb 7. — View Citation

Hendelman D, Miller K, Baggett C, Debold E, Freedson P. Validity of accelerometry for the assessment of moderate intensity physical activity in the field. Med Sci Sports Exerc. 2000 Sep;32(9 Suppl):S442-9. — View Citation

Rodríguez-Merchan EC, Goddard NJ, Lee CA, editors. Musculoskeletal Aspects of Haemophilia. Oxford: Blackwell Sciencie Ltd; 2000.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline in the physiotherapy treatment compliance. Parameters: Intensity, duration, type of exercise and % of compliance.	Level of treatment compliance assessed by the intensity (counts/min), duration (m) and type of exercise measured with triaxial accelerometer.	After 6, 12, 18 and 24 months.
Secondary	Age (years).	Age of patient.	In month 0, and month 24.
Secondary	Weight (Kg).	Weight of patient.	In month 0, and month 24.
Secondary	Biochemistry and haemogram tests. The parameters to be reported are: Leukocyte (mil/mm3), Lymphocyte (mil/mm3), Haemoglobin (g/dl), Glucose (mg/dl), Total, HDL and LDL cholesterol (mg/dl), Triglyceride (mg/dl) and Creatine phosphokinase (CPK) (UI/L).		In Baseline and after 6, 12, 18 and 24 months.
Secondary	Prophylactic treatment with Factor VIII. Parameters: Trough levels of FVIII in blood (% FVIII) and type of FVIII and dose (UI/ week).		In Baseline and after 6, 12, 18 and 24 months.
Secondary	Body composition of patient. Parameters: BMI (Kg/m^2) and % of body fat.		In Baseline and after 6, 12, 18 and 24 months.
Secondary	Cardiovascular condition. Parameters: Beats/minute and distance covered (metres).	Beats/minute measured with a pulse monitor and distance covered in Six-minute walk test (6MWT).	In Baseline and after 6, 12, 18 and 24 months.
Secondary	Blood pressure (mmHg).	Measured with Cuff- stethoscope; Manometer; manual meter.	In Baseline and after 6, 12, 18 and 24 months.
Secondary	Muscle strength in kilos (peak force and time to reach peak force).	Measured with Lafayette device.	In Baseline and after 6, 12, 18 and 24 months.
Secondary	State of joints and injury control (HJHS 2.1. score).	Evaluated by ultrasound system.	In Baseline and after 6, 12, 18 and 24 months.
Secondary	Joint inflammation. Parameters: Thermal imaging (ºC) and joint perimeter (cm).	Measured with thermal camera and tape measure.	In Baseline and after 6, 12, 18 and 24 months.
Secondary	Bone density. Parameter: Bone Quality Index (BQI).	Densitometry.	In Baseline and in month 24.
Secondary	Bleeding/ hemarthrosis. Parameter: Bleeding Rate (BR).	Registered in patient's diary.	In Baseline and after 6, 12, 18 and 24 months.
Secondary	Health-related quality of life. Parameters: General questionnaire (EQ-5D EuroQoL) and specific questionnaire (A36 Hemophilia QoL).		In Baseline and in 12 and 24 month.

External Links

•   Global Recommendations on Physical Activity for Health, WHO.