Abstract
Ethnic differences in disease susceptibility and drug response necessitate the participation of the community in biomedical research. Public involvement includes the donation of biospecimens for basic and translational research with a focus on understanding the molecular make-up of individuals. A growing strategy that fosters public involvement is establishing biobanks that serve as a focal point for sample collection, storage, and dissemination. A biobank's success is dependent on the availability of high-quality biospecimens, as well as accessibility of personal and medical data. Diverse public participation in biobanks is also as critical. Due to lack of data related to public knowledge and attitude towards biospecimen-based research and their willingness to participate in biobanking, a structured questionnaire was conducted at the national level. Data were collected from 3196 individuals aged 18 and above, constituting a representative sample of the Jordanian population. Demographic data included age, gender, and education level. Although there was lack of knowledge of the term "biological samples," 80% of respondents approved the use of biospecimens in research. In addition, almost two-thirds of respondents agreed to donate both biospecimens and relevant information for biobanking. Approval of biospecimen-based research and willingness to participate in biobanking significantly correlated with younger age and increasing education, but not gender. Our results provide an insight into the perception of biobanking among the Jordanian population and strengthen the importance of educating the public about research and the value of biobanking. The data should enable researchers in Jordan and surrounding countries of similar culture to lay the foundation for a successful biobank and research program.
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