Literature DB >> 19705165

What do palliative care patients and their relatives think about research in palliative care?-a systematic review.

Clare White1, Janet Hardy.   

Abstract

INTRODUCTION: Research in palliative care patients has been controversial and is often challenging. It is important to know the views of potentially eligible patients themselves in order to determine the appropriateness of research in the palliative care population and to develop realistic studies that are practical and achievable in this population. This systematic review aims to identify the views of palliative care patients and their families towards research, the factors that are important when considering participation, and the types of research trial they would support or reject.
METHODS: A systematic literature review was undertaken to identify what is known to date regarding the views of palliative care patients and their relatives towards research participation. Eight relevant studies were identified. DISCUSSION: There is an increasing body of evidence considering the views of palliative care patients towards research in palliative care. However, only three studies have considered the views of their relatives/caregivers. Several common themes emerged from the literature including the potential for personal gain, altruism, the wish to avoid complex studies and a desire to retain autonomy. Trial-related factors were also important determinants of willingness of patients and relatives to participate in research. The views expressed by palliative care patients towards research are similar to those of other patient populations.
CONCLUSION: Research to date in the palliative care setting has suggested that patients are interested in participating in research and may actually benefit from doing so.

Entities:  

Mesh:

Year:  2009        PMID: 19705165     DOI: 10.1007/s00520-009-0724-1

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  17 in total

1.  Clinical research in palliative care: patient populations, symptoms, interventions and endpoints.

Authors:  C Mazzocato; C Sweeney; E Bruera
Journal:  Palliat Med       Date:  2001-03       Impact factor: 4.762

2.  Evidence in palliative care research: how should it be gathered?

Authors:  Tania Shelby-James; Amy P Abernethy; David C Currow
Journal:  Med J Aust       Date:  2006-02-20       Impact factor: 7.738

3.  Attitudes of patients to randomised clinical trials of cancer therapy.

Authors:  L J Fallowfield; V Jenkins; C Brennan; M Sawtell; C Moynihan; R L Souhami
Journal:  Eur J Cancer       Date:  1998-09       Impact factor: 9.162

Review 4.  Placebo-controlled trials in palliative care: the argument for.

Authors:  J R Hardy
Journal:  Palliat Med       Date:  1997-09       Impact factor: 4.762

5.  Attitudes towards clinical research amongst participants and nonparticipants.

Authors:  S M Madsen; M R Mirza; S Holm; K L Hilsted; K Kampmann; P Riis
Journal:  J Intern Med       Date:  2002-02       Impact factor: 8.989

6.  Hospice patients' views on research in palliative care.

Authors:  W Terry; L G Olson; P Ravenscroft; L Wilss; G Boulton-Lewis
Journal:  Intern Med J       Date:  2006-07       Impact factor: 2.048

7.  Patients' willingness to enter clinical trials: measuring the association with perceived benefit and preference for decision participation.

Authors:  H A Llewellyn-Thomas; M J McGreal; E C Thiel; S Fine; C Erlichman
Journal:  Soc Sci Med       Date:  1991       Impact factor: 4.634

8.  Issues and dilemmas in conducting research with vulnerable home hospice participants.

Authors:  Marjorie C Dobratz
Journal:  J Nurs Scholarsh       Date:  2003       Impact factor: 3.176

9.  Attitudes of patients and staff to research in a specialist palliative care unit.

Authors:  Catriona Ross; Mike Cornbleet
Journal:  Palliat Med       Date:  2003-09       Impact factor: 4.762

10.  Reasons for accepting or declining to participate in randomized clinical trials for cancer therapy.

Authors:  V Jenkins; L Fallowfield
Journal:  Br J Cancer       Date:  2000-06       Impact factor: 7.640

View more
  22 in total

1.  Conducting research interviews with bereaved family carers: when do we ask?

Authors:  Brenda Bentley; Moira O'Connor
Journal:  J Palliat Med       Date:  2014-12-17       Impact factor: 2.947

2.  Compassion and vigilance: investigators' strategies to manage ethical concerns in palliative and end-of-life research.

Authors:  Susan E Hickman; Juliana C Cartwright; Christine A Nelson; Kathleen Knafl
Journal:  J Palliat Med       Date:  2012-06-25       Impact factor: 2.947

3.  The effect of multiple recruitment contacts on response rates and patterns of missing data in a survey of bladder cancer survivors 6 months after cystectomy.

Authors:  Joanna E Bulkley; Maureen O'Keeffe-Rosetti; Christopher S Wendel; James V Davis; Kim N Danforth; Teresa N Harrison; Marilyn L Kwan; Julie Munneke; Neon Brooks; Marcia Grant; Michael C Leo; Matthew Banegas; Sheila Weinmann; Carmit K McMullen
Journal:  Qual Life Res       Date:  2019-12-06       Impact factor: 4.147

4.  Caregiver-guided pain coping skills training for patients with advanced cancer: Background, design, and challenges for the CaringPals study.

Authors:  Laura S Porter; Gregory Samsa; Jennifer L Steel; Laura C Hanson; Thomas W LeBlanc; Janet Bull; Stacy Fischer; Francis J Keefe
Journal:  Clin Trials       Date:  2019-02-19       Impact factor: 2.486

5.  Ethical conduct of palliative care research: enhancing communication between investigators and institutional review boards.

Authors:  Amy P Abernethy; Warren H Capell; Noreen M Aziz; Christine Ritchie; Maryjo Prince-Paul; Rachael E Bennett; Jean S Kutner
Journal:  J Pain Symptom Manage       Date:  2014-05-28       Impact factor: 3.612

6.  Overcoming recruitment challenges in palliative care clinical trials.

Authors:  Thomas W LeBlanc; Jordan E Lodato; David C Currow; Amy P Abernethy
Journal:  J Oncol Pract       Date:  2013-10-15       Impact factor: 3.840

7.  Symptom Control Trials in Patients With Advanced Cancer: A Qualitative Study.

Authors:  Tom Middlemiss; Mari Lloyd-Williams; Barry J Laird; Marie T Fallon
Journal:  J Pain Symptom Manage       Date:  2015-05-29       Impact factor: 3.612

8.  End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation study.

Authors:  Stephanie Stiel; Maria Heckel; Sonja Bussmann; Martin Weber; Christoph Ostgathe
Journal:  BMC Palliat Care       Date:  2015-05-02       Impact factor: 3.234

9.  Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise.

Authors:  Morag Farquhar; Nancy Preston; Catherine J Evans; Gunn Grande; Vicky Short; Hamid Benalia; Irene J Higginson; Chris Todd
Journal:  J Palliat Med       Date:  2013-11-06       Impact factor: 2.947

10.  Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.

Authors:  Marjolein H Gysels; Catherine Evans; Irene J Higginson
Journal:  BMC Med Res Methodol       Date:  2012-08-17       Impact factor: 4.615

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.