Haemophilia Clinical Trial
Official title:
Sociodemographic, Clinic and Psychosocial Aspects of People With Haemophilia in Portugal: a National Survey
The purpose of this study is to implement a national survey to collect information regarding Portuguese people with haemophilia (PWH) on socio-demographic, clinical and psychosocial factors.
This is a cross-sectional design investigation focused on the socio-demographic, clinical
and psychosocial characterization of Portuguese people with haemophilia (PWH). All PWH,
registered in the Portuguese Hemophilia Association (APH) will be identified in APH
registries and contacted through mail, in order to be invited to participate in the first
Portuguese survey on haemophilia. In case of acceptance, patients must sign the Informed
Consent, fill in the questionnaires and send both back to the investigation team through a
pre-paid envelope in the national mail system.
PWH of all ages are invited to participate in this survey. Adults (aged 18 and over) and
children/youth from 10 to 17 will answer the questionnaires by self report. Parents of small
children (0 to 9) will fill in the proxy versions. All questionnaires are adapted for the
specific age groups.
This study will comply with ethic guidelines and was approved by the Life Sciences and
Health Ethics Subcommittee (University of Minho) and is registered on the Portuguese
authority for data collection (CNPD).
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