Literature DB >> 17896312

Qualitative research methodology in the exploration of patients' perceptions of participating in a genetic research program.

Frieda Basson1, Merle Joyce Futter, Jacquie Greenberg.   

Abstract

The success of genetic research studies depend on patients' willingness to participate. It is thus important to explore the attitudes of individuals that participate in such studies. This study used qualitative methods to explore how individuals with inherited retinal degenerative disorders (RDD) perceived participating in genetic research and subsequently receiving mutation results. Individual interviews were conducted with all the individuals in the Cape Town Metropolitan area who had received mutation results after participating in a genetic research program (4 individuals). Although experiences differed significantly, the study revealed that the participants had positive attitudes towards participating in the RDD research program. This study illustrates the importance of using qualitative methods in ophthalmic populations to explore important issues.

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Year:  2007        PMID: 17896312     DOI: 10.1080/13816810701356627

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  8 in total

1.  Genetic testing and counseling for hereditary neurological diseases in Mali.

Authors:  Katherine Gloria Meilleur; Souleymane Coulibaly; Moussa Traoré; Guida Landouré; Alison La Pean; Modibo Sangaré; Fanny Mochel; Siona Traoré; Kenneth H Fischbeck; Hae-Ra Han
Journal:  J Community Genet       Date:  2011-02-22

2.  Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research.

Authors:  Bradley D Freeman; Carie R Kennedy; Dragana Bolcic-Jankovic; Alexander Eastman; Ellen Iverson; Erica Shehane; Aaron Celious; Jennifer Barillas; Brian Clarridge
Journal:  J Empir Res Hum Res Ethics       Date:  2012-02       Impact factor: 1.742

3.  Return of individual research results from genomic research: A systematic review of stakeholder perspectives.

Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Mwenza Blell; Isabelle Budin-Ljøsne; Lorraine Cowley; Stephanie O M Dyke; Clara Gaff; Robert Green; Alison Hall; Amber L Johns; Bartha M Knoppers; Stephanie Mulrine; Christine Patch; Eva Winkler; Madeleine J Murtagh
Journal:  PLoS One       Date:  2021-11-08       Impact factor: 3.240

4.  "To perpetuate blindness!": attitudes of UK patients with inherited retinal disease towards genetic testing.

Authors:  Barbara Potrata; Martin McKibbin; Jennifer Nw Lim; Jenny Hewison
Journal:  J Community Genet       Date:  2013-12-24

Review 5.  Views on genomic research result delivery methods and informed consent: a review.

Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Madeleine J Murtagh
Journal:  Per Med       Date:  2021-04-06       Impact factor: 2.512

6.  Participants' Preferences and Reasons for Wanting Feedback of Individual Genetic Research Results From an HIV-TB Genomic Study: A Case Study From Botswana.

Authors:  Dimpho Ralefala; Mary Kasule; Olivia P Matshabane; Ambroise Wonkam; Mogomotsi Matshaba; Jantina de Vries
Journal:  J Empir Res Hum Res Ethics       Date:  2021-12       Impact factor: 1.742

7.  Management of a South African family with retinitis pigmentosa-should potential therapy influence translational research protocols?

Authors:  Lisa Roberts; George Rebello; Rajkumar Ramesar; Jacquie Greenberg
Journal:  J Ocul Biol Dis Infor       Date:  2008-05-29

8.  Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results.

Authors:  Alisa D Blazek; Daniel D Kinnamon; Elizabeth Jordan; Hanyu Ni; Ray E Hershberger
Journal:  Clin Transl Sci       Date:  2020-10-27       Impact factor: 4.689

  8 in total

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