An investigation of patients' motivations for their participation in genetics-related research.
about
The tension between data sharing and the protection of privacy in genomics researchBanking the brain. Addressing the ethical challenges of a mental-health biobankPublics and biobanks: Pan-European diversity and the challenge of responsible innovationAccessing health services through the back door: a qualitative interview study investigating reasons why people participate in health research in Canada.Motivations for participating in a non-interventional gender-based violence survey in a low-income setting in South AfricaMotives for participating in a web-based nutrition cohort according to sociodemographic, lifestyle, and health characteristics: the NutriNet-Santé cohort study.Research participant-centered outcomes at NIH-supported clinical research centers.Flexible positions, managed hopes: the promissory bioeconomy of a whole genome sequencing cancer study.Understandings of Participation in Behavioural Research: A Qualitative Study of Gay and Bisexual Men in Scotland.Participants' Understanding of Informed Consent in a Randomized Controlled Trial for Chronic Knee Pain.Key Stakeholders' Perceptions of Motivators for Research Participation Among Individuals Who Are Incarcerated."We're checking them out": Indigenous and non-Indigenous research participants' accounts of deciding to be involved in research.Understanding involvement in surgical orthopaedic randomized controlled trials: A qualitative study of patient and health professional views and experiences.Assessing research participants' perceptions of their clinical research experiencesImpact of Genetic Counseling and Testing on Altruistic Motivations to Test for BRCA1/2: a Longitudinal Study.A new simple six-step model to promote recruitment to RCTs was developed and successfully implemented.The effects of cancer research participation on patient experience: a mixed-methods analysis.The Sexunzipped trial: young people's views of participating in an online randomized controlled trial.Trial participation as avoidance strategy: a qualitative study.Researchers' and clinicians' perceptions of recruiting participants to clinical research: a thematic meta-synthesis.Why do participants enroll in population biobank studies? A systematic literature review.Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.Coproduction of Research Questions and Research Evidence in Public Health: The Study to Prevent Teen Drinking Parties.How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.Women's experiences of participating in a prospective, longitudinal postpartum depression study: insights for perinatal mental health researchers.US Military Service Members' Reasons for Deciding to Participate in Health Research.Participation in Genetic Research: Amazon's Mechanical Turk Workforce in the United States and India.Parents' perspectives on participating in genetic research in autism.Potential motivations for and perceived risks in research participation: ethics in health research.Typologies of Altruistic and Financial Motivations for Research ParticipationSuccessful blood salvaging from preterm infants: maximizing opportunities, minimizing interventions.Learning from older peoples' reasons for participating in demanding, intensive epidemiological studies: a qualitative study.Genomic medicine for kidney disease.Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results.Patient-initiated recruitment for clinical research: Evaluation of an outpatient letter research statement.Public trust and 'ethics review' as a commodity: the case of Genomics England Limited and the UK's 100,000 genomes project.The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.Participants' Accounts on Their Decision to Join a Cohort Study With an Attached Biobank: A Qualitative Content Analysis Study Within Two German Studies.The Meanings of Helping: An Analysis of Cystic Fibrosis Patients' Reasons for Participating in Biomedical Research.Appealing to altruism is not enough: motivators for participating in health services research.
P2860
Q26866269-EC2E6F98-3D7E-4D42-B1D3-1C57FEE36674Q28706268-18251DA5-BE23-4345-8573-D9D2446F742BQ30529892-7F7584D9-11BA-4187-B2FA-F7E2C7EE00B1Q30558791-324480CF-985C-4767-9174-5CDBB34A668EQ32174185-68F59BEB-16D6-4D25-B1CB-14FE10019A3BQ34062905-44E67E93-9CC7-446A-AA1D-A3301429EFB6Q34543697-442FAE2B-EC31-47E2-9778-E835002C49AAQ35187045-13A0D3F7-7286-434D-AAD8-94E42939A0A5Q35739802-85E7CEC7-F9C1-499D-B12A-4760D5DEF09CQ35813928-A3D55392-14AE-4CCA-B743-50DE861334F7Q36073293-865FA7BC-A829-4D8B-9483-B865053F9D01Q36469165-B90AAD3C-17C0-48C9-8A61-34E15C837B2AQ36484931-8A40A666-AB94-4BE2-A21A-8155AF309E1EQ36808362-90B6E189-4968-4C06-8276-A3BE1F72D347Q36909418-5DB8233E-C93A-4E01-A1D1-F007FCE8542DQ37301484-2B758B4A-D53D-4CC3-930C-9FBF6C19980CQ37394054-5264C060-910C-442B-8A07-4689AA8FE4E9Q37405586-28FB9F45-2CA8-4FB2-A063-D0ADEF4D7E3FQ37476500-2086D994-BE4B-49B5-862A-DE2369837B3CQ37701141-4144EE70-2A0D-4C1E-88F1-65D2AE304DEBQ38068936-7FC0A536-A707-46F1-805D-D99399021E43Q38633533-EF921E75-8AB2-4359-BB91-1155B18425DDQ38659656-B2A51518-5B22-4F18-BCC9-1C3C8EC52CC0Q38730932-DDCE6DD8-97FB-4030-85CC-4042FA142741Q38732935-9AB187BC-A0C6-42A6-99C8-AB8D79389621Q38759080-033151BD-5B7A-4862-A9B3-7B226088BE50Q39218001-953B8F1A-5400-4FBB-805C-0EAB2452268EQ39588412-28CCAC98-E85B-4109-9CE4-A1A3B5D665F0Q40110141-4C751368-05E0-413B-B70B-5F26339C89A2Q41647548-90B3C1ED-8179-4AA3-A92F-01AAAA5524EEQ43855161-1D1102E0-9CD2-47EC-98F8-61F1BCFEA278Q47162752-6695BB3B-7450-45C1-9558-9E7CC70E3D07Q47200436-12559516-2C94-464B-89BE-8614A75E87B5Q47319704-3DAB4495-0930-4C6D-84EF-8B614D48D4ACQ47430181-0A71FC16-A5E5-4F71-974C-7F5838164A08Q47633296-EC4118C3-EFCB-4CCD-9921-5D7FD847CB9FQ47701862-3948DD94-9319-4EFF-9DD0-896FB75323C8Q47707041-E1C3450B-F7A5-48D1-BAB9-BE0725E03892Q47833640-8CAF4A96-F6AD-4B0B-8951-04ECE64F87ABQ47970103-A0E4DC71-B940-455D-AC54-363B23E717DA
P2860
An investigation of patients' motivations for their participation in genetics-related research.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
An investigation of patients' ...... in genetics-related research.
@en
An investigation of patients' ...... in genetics-related research.
@nl
type
label
An investigation of patients' ...... in genetics-related research.
@en
An investigation of patients' ...... in genetics-related research.
@nl
prefLabel
An investigation of patients' ...... in genetics-related research.
@en
An investigation of patients' ...... in genetics-related research.
@nl
P2093
P356
P1476
An investigation of patients' ...... in genetics-related research.
@en
P2093
P356
10.1136/JME.2009.029264
P577
2010-01-01T00:00:00Z