Brief Title
Comparing the Burden of Illness of Hemophilia in the Developing and the Developed World
Official Title
Comparing the Burden of Illness of Hemophilia in the Developing and the Developed World: The Sao Paulo - Toronto Hemophilia Study
Brief Summary
Because of high cost, persons with hemophilia in many developing countries cannot afford adequate treatment. For example, many persons with hemophilia in India and China are only rarely treated with factor replacement in response to bleeds, and as a result many have developed significant arthropathy and disability. A pilot study in China estimated the mean Hemophilia Joint Health Score (HJHS) at 13.1 (SD 9.03) suggesting that these children had highly prevalent, severe joint disease. The lack of relationship between the HJHS and treatment history suggests overall inadequate therapy. The proposed study will quantify the burden of arthropathy, physical disability, and quality of life (QoL) in boys with hemophilia in Brazil - where comprehensive treatment is just beginning to be widely available. This study will also provide an opportunity to compare these outcomes to those observed in Canada, where the dominant therapy has become life-long prophylaxis.
Detailed Description
In order to quantify the burden of illness in hemophilia, and to study the response to different treatments, it is necessary to have quantitative outcome measures of high validity and reliability. The International Prophylaxis Study Group (IPSG - chair Dr. Victor Blanchette) was established in 2001 with the stated purpose of developing and testing outcome tools for this purpose. The group has developed a magnetic resonance imaging (MRI) score for quantifying arthropathy (representing the domain of structure and function domain in the ICF framework), a quantitative physical examination score, and the Hemophilia Joint Health Score or HJHS, to replace the older and less sensitive World Federation of Hemophilia (WFH) score (representing the domain of structure and function in the ICF). In addition Canadian investigators have also developed a quality of life measure for boys with hemophilia, the Canadian Hemophilia Outcomes Kids' Life Assessment Tool or CHO-KLAT (representing the domain of participation in the ICF). We will use these tools, and other validated measures, to begin to determine the burden of hemophilia in Brazil and compare it to the burden of disease in Canada. Additionally, we will use this study to demonstrate the validity of these tools in the Brazilian population.
Study Type
Observational
Primary Outcome
Burden of Illness
Secondary Outcome
The Activity Scale for Kids (ASK)
Condition
Hemophilia A
Study Arms / Comparison Groups
Brazilian Subject's
Description: Subject's will be recruited from the Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paolo (HCFMUSP); Universidade Estadual de Campinas (UNICAMP); Universidade Federal de São Paulo (UNIFESP)
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Estimated Enrollment
100
Start Date
September 2010
Completion Date
October 2013
Primary Completion Date
October 2013
Eligibility Criteria
Inclusion criteria - Hemophilia A or B moderate or severe as determined by serum factor activity ≤ 5% - Age 7 - 18 yrs. inclusive - At least one parent or guardian fluent in written Portuguese or English and able to complete the study outcome questionnaires. Exclusion criteria - None (Children with inhibitors will be allowed into the study for 2 reasons: i) our study aims to document the health of persons with hemophilia in a generalizable way, ii) not all children will have had inhibitor testing done.)
Gender
Male
Ages
7 Years - 18 Years
Accepts Healthy Volunteers
No
Contacts
Brain M. Feldman, MD,MSc,FRCPC, ,
Location Countries
Brazil
Location Countries
Brazil
Administrative Informations
NCT ID
NCT01217255
Organization ID
1000020214
Responsible Party
Principal Investigator
Study Sponsor
The Hospital for Sick Children
Study Sponsor
Brain M. Feldman, MD,MSc,FRCPC, Principal Investigator, The Hospital for Sick Children
Verification Date
June 2018