Literature DB >> 20926403

Predicting intention to biobank: a national survey.

Christine R Critchley1, Dianne Nicol, Margaret F A Otlowski, Mark J A Stranger.   

Abstract

BACKGROUND: The success of human population biobanks are dependent on the publics' willingness to participate. This research aimed to determine those factors important in determining the public's intention to donate a biological sample to a publicly funded biobank, and allow that sample to be linked with medical records.
METHODS: A national sample of 1000 Australians was surveyed via telephonic interviews. Questions included the reported likelihood that respondents would participate in biobank research, ratings of trust in biobanks, beliefs that biobank research will lead to improved health care and general ratings of comfort with blood taking and DNA analysis.
RESULTS: The sample reported a high level of trust in university biobanks, a strong belief that biobank research will lead to improved health care and a strong willingness to participate in biobank research. Using structural equation modelling, trust in the biobank was found to be the most important determinant of intention to participate in biobank research, followed by general comfort with blood taking and DNA analysis, belief in health-care benefits and higher education. Gender, age, parental status and experience of genetic conditions were not significantly associated with intention to participate.
CONCLUSIONS: Australians are generally willing to participate in biobank research, and this is strongly determined by trust. While benefit beliefs and comfort with research are also relevant, higher trust was associated with intention regardless of these factors, suggesting reasons other than concern for improved health care are important in determining the publics' willingness to participate in biobank research.

Entities:  

Mesh:

Year:  2010        PMID: 20926403     DOI: 10.1093/eurpub/ckq136

Source DB:  PubMed          Journal:  Eur J Public Health        ISSN: 1101-1262            Impact factor:   3.367


  27 in total

1.  Don't take your EHR to heaven, donate it to science: legal and research policies for EHR post mortem.

Authors:  Vojtech Huser; James J Cimino
Journal:  J Am Med Inform Assoc       Date:  2013-08-21       Impact factor: 4.497

2.  Biobanks and the phantom public.

Authors:  Herbert Gottweis; Haidan Chen; Johannes Starkbaum
Journal:  Hum Genet       Date:  2011-07-20       Impact factor: 4.132

3.  Public support and consent preference for biomedical research and biobanking in Jordan.

Authors:  Mamoun Ahram; Areej Othman; Manal Shahrouri
Journal:  Eur J Hum Genet       Date:  2012-09-12       Impact factor: 4.246

4.  Industry involvement in publicly funded biobanks.

Authors:  Timothy Caulfield; Pascal Borry; Herbert Gottweis
Journal:  Nat Rev Genet       Date:  2014-04       Impact factor: 53.242

5.  Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.

Authors:  J M Oliver; M J Slashinski; T Wang; P A Kelly; S G Hilsenbeck; A L McGuire
Journal:  Public Health Genomics       Date:  2011-12-30       Impact factor: 2.000

6.  Development and validation of the biobanking attitudes and knowledge survey (BANKS).

Authors:  Kristen J Wells; Mariana Arevalo; Cathy D Meade; Clement K Gwede; Gwendolyn P Quinn; John S Luque; Gloria San Miguel; Dale Watson; Rebecca Phillips; Carmen Reyes; Margarita Romo; Jim West; Paul B Jacobsen
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2014-03       Impact factor: 4.254

7.  "As Long as You Ask": A Qualitative Study of Biobanking Consent-Oncology Patients' and Health Care Professionals' Attitudes, Motivations, and Experiences-the B-PPAE Study.

Authors:  Sonia Yip; Jennifer Fleming; Heather L Shepherd; Adam Walczak; Jonathan Clark; Phyllis Butow
Journal:  Oncologist       Date:  2018-11-09

8.  Development and Validation of the Biomedical Research Trust Scale (BRTS) in English and Spanish.

Authors:  Sharon H Baik; Mariana Arevalo; Clement Gwede; Cathy D Meade; Paul B Jacobsen; Gwendolyn P Quinn; Kristen J Wells
Journal:  J Empir Res Hum Res Ethics       Date:  2016-09-21       Impact factor: 1.742

9.  Patients' willingness to participate in a breast cancer biobank at screening mammogram.

Authors:  Christoph I Lee; Lawrence W Bassett; Mei Leng; Sally L Maliski; Bryan B Pezeshki; Colin J Wells; Carol M Mangione; Arash Naeim
Journal:  Breast Cancer Res Treat       Date:  2012-11-06       Impact factor: 4.872

10.  Willingness of women to participate in obstetrical and pediatric research involving biobanks.

Authors:  Renate D Savich; Beth B Tigges; Lisbeth Iglesias Rios; Joanne McCloskey; Kristine Tollestrup; Robert D Annett
Journal:  J Community Genet       Date:  2019-11-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.