Literature DB >> 10940136

Patient participation in research in the managed care environment: key perceptions of members in an HMO.

S Purdy1, J A Finkelstein, R Fletcher, C Christiansen, T S Inui.   

Abstract

This study's objective was to elicit the views of research among enrollees in an HMO. A questionnaire was mailed to 207 adult enrollees, 55% had been exposed to research and 45% had not. Ninety-four percent of respondents supported research within the HMO, and 87% thought using information from medical records for research was acceptable. Sixty-three percent thought participation in research increased patient understanding of health care. Significantly more prior research participants thought that participation in research improves care. More patients would participate if written information were provided (67%), if feedback of results was provided (72%), and if their clinician invited them (67%). Only a modest percentage (20%) of patients would participate in a randomized trial.

Entities:  

Mesh:

Year:  2000        PMID: 10940136      PMCID: PMC1495479          DOI: 10.1046/j.1525-1497.2000.07025.x

Source DB:  PubMed          Journal:  J Gen Intern Med        ISSN: 0884-8734            Impact factor:   5.128


  19 in total

1.  Health of the public: The private-sector challenge.

Authors:  J Showstack; N Lurie; S Leatherman; E Fisher; T Inui
Journal:  JAMA       Date:  1996-10-02       Impact factor: 56.272

2.  The impact of managed care on clinical research: a preliminary investigation.

Authors:  R E Mechanic; A Dobson
Journal:  Health Aff (Millwood)       Date:  1996       Impact factor: 6.301

3.  Effect of managed care felt in every medical field.

Authors:  C Marwick
Journal:  JAMA       Date:  1996-09-11       Impact factor: 56.272

4.  Trust, The fragile foundation of contemporary biomedical research.

Authors:  N E Kass; J Sugarman; R Faden; M Schoch-Spana
Journal:  Hastings Cent Rep       Date:  1996 Sep-Oct       Impact factor: 2.683

5.  Motives and perception of healthy volunteers who participate in experiments.

Authors:  C E van Gelderen; T J Savelkoul; W van Dokkum; J Meulenbelt
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

6.  Academic medical centers under siege.

Authors:  J P Kassirer
Journal:  N Engl J Med       Date:  1994-11-17       Impact factor: 91.245

7.  The "teaching HMO": a new academic partner.

Authors:  G T Moore; T S Inui; J M Ludden; S C Schoenbaum
Journal:  Acad Med       Date:  1994-08       Impact factor: 6.893

8.  Does practice location or academic connection affect recruitment of patients as research subjects?

Authors:  R B Kelly; S H McMahon; J A Hazey
Journal:  Fam Pract Res J       Date:  1992-06

9.  Patients' attitudes to participation in clinical trials.

Authors:  E G Bevan; L C Chee; S M McGhee; G T McInnes
Journal:  Br J Clin Pharmacol       Date:  1993-02       Impact factor: 4.335

10.  Research collaboration between an HMO and an academic medical center: lessons learned.

Authors:  D C Donahue; B E Lewis; I S Ockene; G Saperia
Journal:  Acad Med       Date:  1996-02       Impact factor: 6.893

View more
  7 in total

1.  Recruitment and retention of pregnant women into clinical research trials: an overview of challenges, facilitators, and best practices.

Authors:  Paula M Frew; Diane S Saint-Victor; Margaret Brewinski Isaacs; Sonnie Kim; Geeta K Swamy; Jeanne S Sheffield; Kathryn M Edwards; Tonya Villafana; Ouda Kamagate; Kevin Ault
Journal:  Clin Infect Dis       Date:  2014-12-15       Impact factor: 9.079

2.  Preferences for the research use of electronic health records among young adults with fragile X syndrome or autism spectrum disorder.

Authors:  Laura Wagner; MaryKate Frisch; Lauren Turner-Brown; Sara Andrews; Anne Edwards; Rebecca Moultrie; Alexandra Alvarez Rivas; Anne Wheeler; Melissa Raspa
Journal:  Disabil Health J       Date:  2020-04-08       Impact factor: 2.554

3.  Patient attitudes to clinical trials: development of a questionnaire and results from asthma and cancer patients.

Authors:  Crispin Jenkinson; John S Burton; Julia Cartwright; Helen Magee; Ian Hall; Chris Alcock; Sherwood Burge
Journal:  Health Expect       Date:  2005-09       Impact factor: 3.377

4.  User Involvement in Myasthenia Gravis Research.

Authors:  Nils Erik Gilhus; Sandra Iren Barkås Hovland
Journal:  Front Neurol       Date:  2022-06-02       Impact factor: 4.086

5.  Genomic research and wide data sharing: views of prospective participants.

Authors:  Susan Brown Trinidad; Stephanie M Fullerton; Julie M Bares; Gail P Jarvik; Eric B Larson; Wylie Burke
Journal:  Genet Med       Date:  2010-08       Impact factor: 8.822

Review 6.  Ethical, Legal, and Social Issues Related to the Inclusion of Individuals With Intellectual Disabilities in Electronic Health Record Research: Scoping Review.

Authors:  Melissa Raspa; Rebecca Moultrie; Laura Wagner; Anne Edwards; Sara Andrews; Mary Katherine Frisch; Lauren Turner-Brown; Anne Wheeler
Journal:  J Med Internet Res       Date:  2020-05-21       Impact factor: 5.428

7.  Informed consent from patients participating in medical education: a survey from a university hospital in Jamaica.

Authors:  Alan T Barnett; Shamir O Cawich; Ivor W Crandon; John F Lindo; Georgiana Gordon-Strachan; Diaqa Robinson; Deonne Ranglin
Journal:  BMC Res Notes       Date:  2009-12-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.