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Published in: BMC Palliative Care 1/2012

Open Access 01-12-2012 | Study protocol

A region-based palliative care intervention trial using the mixed-method approach: Japan OPTIM study

Authors: Tatsuya Morita, Mitsunori Miyashita, Akemi Yamagishi, Nobuya Akizuki, Yoshiyuki Kizawa, Yutaka Shirahige, Miki Akiyama, Kei Hirai, Motohiro Matoba, Masako Yamada, Taketoshi Matsumoto, Takuhiro Yamaguchi, Kenji Eguchi

Published in: BMC Palliative Care | Issue 1/2012

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Abstract

Background

Disseminating palliative care is a critical task throughout the world. Several outcome studies explored the effects of regional palliative care programs on a variety of end-points, and some qualitative studies investigated the process of developing community palliative care networks. These studies provide important insights into the potential benefits of regional palliative care programs, but the clinical implications are still limited, because: 1) many interventions included fundamental changes in the structure of the health care system, and, thus, the results would not be applicable for many regions where structural changes are difficult or unfeasible; 2) patient-oriented outcomes were not measured or explored only in a small number of populations, and interpretation of the results from a patient's view is difficult; and 3) no studies adopted a mixed-method approach using both quantitative and qualitative methodologies to interpret the complex phenomenon from multidimensional perspectives.

Methods/designs

This is a mixed-method regional intervention trial, consisting of a pre-post outcome study and qualitative process studies. The primary aim of the pre-post outcome study is to evaluate the change in the number of home deaths, use of specialized palliative care services, patient-reported quality of palliative care, and family-reported quality of palliative care after regional palliative care intervention. The secondary aim is to explore the changes in a variety of outcomes, including patients' quality of life, pain intensity, family care burden, and physicians' and nurses' knowledge, difficulties, and self-perceived practice. Outcome measurements used in this study include the Care Evaluation Scale, Good Death Inventory, Brief pain Inventory, Caregiving Consequence Inventory, Sense of Security Scale, Palliative Care Knowledge test, Palliative Care Difficulties Scale, and Palliative Care Self-reported Practice Scale. Study populations are a nearly representative sample of advanced cancer patients, bereaved family members, physicians, and nurses in the region.
Qualitative process studies consist of 3 studies with each aim: 1) to describe the process in developing regional palliative care in each local context, 2) to understand how and why the regional palliative care program led to changes in the region and to propose a model for shaping regional palliative care, and 3) to systemically collect the barriers of palliative care at a regional level and potential resolutions. The study methodology is a case descriptive study, a grounded theory approach based on interviews, and a content analysis based on systemically collected data, respectively.

Discussion

This study is, to our knowledge, one of the most comprehensive evaluations of a region-based palliative care intervention program. This study has 3 unique aspects: 1) it measures a wide range of outcomes, including quality of care and quality of life measures specifically designed for palliative care populations, whether patients died where they actually preferred, the changes in physicians and nurses at a regional level; 2) adopts qualitative studies along with quantitative evaluations; and 3) the intervention is without a fundamental change in health care systems. A comprehensive understanding of the findings in this study will contribute to a deeper insight into how to develop community palliative care.

Trial Registration

UMIN Clinical Trials Registry (UMIN-CTR), Japan, UMIN000001274.
Literature
1.
go back to reference World Health Organization: National cancer control programmes: Policies and managerial guidelines second edition. Geneva, WHO. 2002 World Health Organization: National cancer control programmes: Policies and managerial guidelines second edition. Geneva, WHO. 2002
2.
go back to reference Jordhøy MS, Fayers P, Saltnes T, Ahlner-Elmqvist M, Jannert M, Kaasa S: A palliative-care intervention and death at home: a cluster randomised trial. Lancet. 2000, 356: 888-893. 10.1016/S0140-6736(00)02678-7.CrossRefPubMed Jordhøy MS, Fayers P, Saltnes T, Ahlner-Elmqvist M, Jannert M, Kaasa S: A palliative-care intervention and death at home: a cluster randomised trial. Lancet. 2000, 356: 888-893. 10.1016/S0140-6736(00)02678-7.CrossRefPubMed
3.
go back to reference Ringdal GI, Jordhøy MS, Kaasa S: Family satisfaction with end-of-life care for cancer patients in a cluster randomized trial. J Pain Symptom Manage. 2002, 24: 53-63. 10.1016/S0885-3924(02)00417-7.CrossRefPubMed Ringdal GI, Jordhøy MS, Kaasa S: Family satisfaction with end-of-life care for cancer patients in a cluster randomized trial. J Pain Symptom Manage. 2002, 24: 53-63. 10.1016/S0885-3924(02)00417-7.CrossRefPubMed
4.
go back to reference Jordhøy MS, Fayers P, Loge JH, Ahlner-Elmqvist M, Kaasa S: Quality of life in palliative cancer care: results from a cluster randomized trial. J Clin Oncol. 2001, 19: 3884-3894.PubMed Jordhøy MS, Fayers P, Loge JH, Ahlner-Elmqvist M, Kaasa S: Quality of life in palliative cancer care: results from a cluster randomized trial. J Clin Oncol. 2001, 19: 3884-3894.PubMed
5.
go back to reference Fassbender K, Fainsinger R, Brenneis C, Brown P, Braun T, Jacobs P: Utilization and costs of the introduction of system-wide palliative care in Alberta, 1993-2000. Palliat Med. 2005, 19: 513-520. 10.1191/0269216305pm1071oa.CrossRefPubMed Fassbender K, Fainsinger R, Brenneis C, Brown P, Braun T, Jacobs P: Utilization and costs of the introduction of system-wide palliative care in Alberta, 1993-2000. Palliat Med. 2005, 19: 513-520. 10.1191/0269216305pm1071oa.CrossRefPubMed
6.
7.
go back to reference Dudgeon DJ, Knott C, Chapman C, Coulson K, Jeffery E, Preston S, Eichholz M, Van Dijk JP, Smith A: Development, implementation, and process evaluation of a regional palliative care quality improvement project. J Pain Symptom Manage. 2009, 38: 483-495. 10.1016/j.jpainsymman.2008.12.006.CrossRefPubMed Dudgeon DJ, Knott C, Chapman C, Coulson K, Jeffery E, Preston S, Eichholz M, Van Dijk JP, Smith A: Development, implementation, and process evaluation of a regional palliative care quality improvement project. J Pain Symptom Manage. 2009, 38: 483-495. 10.1016/j.jpainsymman.2008.12.006.CrossRefPubMed
8.
go back to reference Dudgeon DJ, Knott C, Eichholz M, Gerlach JL, Chapman C, Viola R, Van Dijk J, Preston S, Batchelor D, Bartfay E: Palliative care integration project (PCIP) quality improvement strategy evaluation. J Pain Symptom Manage. 2008, 35: 573-582. 10.1016/j.jpainsymman.2007.07.013.CrossRefPubMed Dudgeon DJ, Knott C, Eichholz M, Gerlach JL, Chapman C, Viola R, Van Dijk J, Preston S, Batchelor D, Bartfay E: Palliative care integration project (PCIP) quality improvement strategy evaluation. J Pain Symptom Manage. 2008, 35: 573-582. 10.1016/j.jpainsymman.2007.07.013.CrossRefPubMed
9.
go back to reference Gómez-Batiste X, Porta-Sales J, Pascual A, Nabal M, Espinosa J, Paz S, Minguell C, Rodríguez D, Esperalba J, Stjernswärd J, Geli M: Palliative Care Advisory Committee of the Standing Advisory Committee for Socio-Health Affairs, Department of Health, Government of Catalonia. Catalonia WHO palliative care demonstration project at 15 years (2005). J Pain Symptom Manage. 2007, 33: 584-590. 10.1016/j.jpainsymman.2007.02.019.CrossRefPubMed Gómez-Batiste X, Porta-Sales J, Pascual A, Nabal M, Espinosa J, Paz S, Minguell C, Rodríguez D, Esperalba J, Stjernswärd J, Geli M: Palliative Care Advisory Committee of the Standing Advisory Committee for Socio-Health Affairs, Department of Health, Government of Catalonia. Catalonia WHO palliative care demonstration project at 15 years (2005). J Pain Symptom Manage. 2007, 33: 584-590. 10.1016/j.jpainsymman.2007.02.019.CrossRefPubMed
10.
go back to reference Shaw KL, Clifford C, Thomas K, Meehan H: Improving end-of-life care: a critical review of the Gold Standards Framework in primary care. Palliat Med. 2010, 24: 317-329. 10.1177/0269216310362005.CrossRefPubMed Shaw KL, Clifford C, Thomas K, Meehan H: Improving end-of-life care: a critical review of the Gold Standards Framework in primary care. Palliat Med. 2010, 24: 317-329. 10.1177/0269216310362005.CrossRefPubMed
11.
go back to reference Munday D, Mohmood K, Dale J, King N: Facilitating good process in primary palliative care: does the Gold Standards Framework enable quality performance?. Fam Pract. 2007, 24: 486-494. 10.1093/fampra/cmm045.CrossRefPubMed Munday D, Mohmood K, Dale J, King N: Facilitating good process in primary palliative care: does the Gold Standards Framework enable quality performance?. Fam Pract. 2007, 24: 486-494. 10.1093/fampra/cmm045.CrossRefPubMed
12.
go back to reference Dale J, Petrova M, Munday D, Koistinen-Harris J, Lall R, Thomas K: A national facilitation project to improve primary palliative care: impact of the Gold Standards Framework on process and self-ratings of quality. Qual Saf Health Care. 2009, 18: 174-180. 10.1136/qshc.2007.024836.CrossRefPubMedPubMedCentral Dale J, Petrova M, Munday D, Koistinen-Harris J, Lall R, Thomas K: A national facilitation project to improve primary palliative care: impact of the Gold Standards Framework on process and self-ratings of quality. Qual Saf Health Care. 2009, 18: 174-180. 10.1136/qshc.2007.024836.CrossRefPubMedPubMedCentral
13.
go back to reference Walsh C, Caress A, Chew-Graham C, Todd C: Implementation and impact of the Gold Standards framework in community palliative care: a qualitative study of three primary care trusts. Palliat Med. 2008, 22: 736-743. 10.1177/0269216308094103.CrossRef Walsh C, Caress A, Chew-Graham C, Todd C: Implementation and impact of the Gold Standards framework in community palliative care: a qualitative study of three primary care trusts. Palliat Med. 2008, 22: 736-743. 10.1177/0269216308094103.CrossRef
14.
go back to reference Kelley ML: Developing rural communities' capacity for palliative care: a conceptual model. J Palliat Care. 2007, 23: 143-153.PubMed Kelley ML: Developing rural communities' capacity for palliative care: a conceptual model. J Palliat Care. 2007, 23: 143-153.PubMed
15.
go back to reference Masso M, Owen A: Linkage, coordination and integration. Evidence from rural palliative care. Aust J Rural Health. 2009, 17: 263-267. 10.1111/j.1440-1584.2009.01089.x.CrossRefPubMed Masso M, Owen A: Linkage, coordination and integration. Evidence from rural palliative care. Aust J Rural Health. 2009, 17: 263-267. 10.1111/j.1440-1584.2009.01089.x.CrossRefPubMed
16.
go back to reference Nikbakht-Van de Sande CV, van der Rijt CC, Visser AP, ten Voorde MA, Pruyn JF: Function of local networks in palliative care: A dutch view. J Palliat Med. 2005, 8: 808-816. 10.1089/jpm.2005.8.808.CrossRefPubMed Nikbakht-Van de Sande CV, van der Rijt CC, Visser AP, ten Voorde MA, Pruyn JF: Function of local networks in palliative care: A dutch view. J Palliat Med. 2005, 8: 808-816. 10.1089/jpm.2005.8.808.CrossRefPubMed
17.
go back to reference Lewin S, Glenton C, Oxman AD: Use of qualitative methods alongside randomised controlled trials of complex healthcare interventions: methodological study. BMJ. 2009, 339: b3496-10.1136/bmj.b3496.CrossRefPubMedPubMedCentral Lewin S, Glenton C, Oxman AD: Use of qualitative methods alongside randomised controlled trials of complex healthcare interventions: methodological study. BMJ. 2009, 339: b3496-10.1136/bmj.b3496.CrossRefPubMedPubMedCentral
18.
go back to reference Oakley A, Strange V, Bonell C, Allen E, Stephenson J, RIPPLE Study Team: Process evaluation in randomised controlled trials of complex interventions. BMJ. 2006, 332: 413-416. 10.1136/bmj.332.7538.413.CrossRefPubMedPubMedCentral Oakley A, Strange V, Bonell C, Allen E, Stephenson J, RIPPLE Study Team: Process evaluation in randomised controlled trials of complex interventions. BMJ. 2006, 332: 413-416. 10.1136/bmj.332.7538.413.CrossRefPubMedPubMedCentral
19.
go back to reference Hawe P, Shiell A, Riley T: Complex interventions: how "out of control" can a randomised controlled trial be?. BMJ. 2004, 328: 1561-1563. 10.1136/bmj.328.7455.1561.CrossRefPubMedPubMedCentral Hawe P, Shiell A, Riley T: Complex interventions: how "out of control" can a randomised controlled trial be?. BMJ. 2004, 328: 1561-1563. 10.1136/bmj.328.7455.1561.CrossRefPubMedPubMedCentral
20.
go back to reference Craig P, Dieppe P, Macintyre S, Michie S, Nazareth I, Petticrew M, Medical Research Council Guidance: Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ. 2008, 337: a1655-10.1136/bmj.a1655.CrossRefPubMedPubMedCentral Craig P, Dieppe P, Macintyre S, Michie S, Nazareth I, Petticrew M, Medical Research Council Guidance: Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ. 2008, 337: a1655-10.1136/bmj.a1655.CrossRefPubMedPubMedCentral
21.
go back to reference Mitchell G: How well do general practitioners deliver palliative care? A systematic review. Palliat Med. 2002, 16: 457-464. 10.1191/0269216302pm573oa.CrossRefPubMed Mitchell G: How well do general practitioners deliver palliative care? A systematic review. Palliat Med. 2002, 16: 457-464. 10.1191/0269216302pm573oa.CrossRefPubMed
22.
go back to reference Ahmed N, Bestall JC, Ahmedzai SH, Payne SA, Clark D, Noble B: Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals. Palliat Med. 2004, 18: 525-542. 10.1191/0269216304pm921oa.CrossRefPubMed Ahmed N, Bestall JC, Ahmedzai SH, Payne SA, Clark D, Noble B: Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals. Palliat Med. 2004, 18: 525-542. 10.1191/0269216304pm921oa.CrossRefPubMed
23.
go back to reference Miyashita M, Sanjo M, Morita T, Hirai K, Kizawa Y, Shima Y, Shimoyama N, Tsuneto S, Hiraga K, Sato K, Uchitomi Y: Barriers to providing palliative care and priorities for future actions to advance palliative care in Japan: a nationwide expert opinion survey. J Palliat Med. 2007, 10: 390-399. 10.1089/jpm.2006.0154.CrossRefPubMed Miyashita M, Sanjo M, Morita T, Hirai K, Kizawa Y, Shima Y, Shimoyama N, Tsuneto S, Hiraga K, Sato K, Uchitomi Y: Barriers to providing palliative care and priorities for future actions to advance palliative care in Japan: a nationwide expert opinion survey. J Palliat Med. 2007, 10: 390-399. 10.1089/jpm.2006.0154.CrossRefPubMed
25.
go back to reference Farmer AP, Légaré F, Turcot L, Grimshaw J, Harvey E, McGowan JL, Wolf F: Printed educational materials: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2008, CD004398-3 Farmer AP, Légaré F, Turcot L, Grimshaw J, Harvey E, McGowan JL, Wolf F: Printed educational materials: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2008, CD004398-3
26.
go back to reference Goldberg GR, Morrison RS: Pain management in hospitalized cancer patients: A systematic review. J Clin Oncol. 2007, 25: 1792-1801. 10.1200/JCO.2006.07.9038.CrossRefPubMed Goldberg GR, Morrison RS: Pain management in hospitalized cancer patients: A systematic review. J Clin Oncol. 2007, 25: 1792-1801. 10.1200/JCO.2006.07.9038.CrossRefPubMed
27.
go back to reference Alvarez MP, Agra Y: Systematic review of educational interventions in palliative care for primary care physicians. Palliat Med. 2006, 20: 673-683. 10.1177/0269216306071794.CrossRefPubMed Alvarez MP, Agra Y: Systematic review of educational interventions in palliative care for primary care physicians. Palliat Med. 2006, 20: 673-683. 10.1177/0269216306071794.CrossRefPubMed
28.
go back to reference Forsetlund L, Bjørndal A, Rashidian A, Jamtvedt G, O'Brien MA, Wolf F, Davis D, Odgaard-Jensen J, Oxman AD: Continuting education meetings and workshops: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2009, CD003030-2 Forsetlund L, Bjørndal A, Rashidian A, Jamtvedt G, O'Brien MA, Wolf F, Davis D, Odgaard-Jensen J, Oxman AD: Continuting education meetings and workshops: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2009, CD003030-2
29.
go back to reference O'Brien MA, Rogers S, Jamtvedt G, Oxman AD, Odgaard-Jensen J, Kristoffersen DT, Forsetlund L, Bainbridge D, Freemantle N, Davis DA, Haynes RB, Harvey EL: Educational outreach visits: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2007, CD000409-4 O'Brien MA, Rogers S, Jamtvedt G, Oxman AD, Odgaard-Jensen J, Kristoffersen DT, Forsetlund L, Bainbridge D, Freemantle N, Davis DA, Haynes RB, Harvey EL: Educational outreach visits: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. 2007, CD000409-4
30.
go back to reference Gysels M, Richardson A, Higginson IJ: Does the patient-held record improve continuity and related outcomes in cancer care: a systematic review. Health Expect. 2006, 10: 75-91.CrossRef Gysels M, Richardson A, Higginson IJ: Does the patient-held record improve continuity and related outcomes in cancer care: a systematic review. Health Expect. 2006, 10: 75-91.CrossRef
31.
go back to reference Fukui S, Fujita J, Tsujimura M, Sumikawa Y, Hayashi Y, Fukui N: Late referrals to home care service affecting death at home in advanced cancer patients in Japan: a nationwide survey. Ann Oncol. 2011, 22: 2113-2120. 10.1093/annonc/mdq719.CrossRefPubMed Fukui S, Fujita J, Tsujimura M, Sumikawa Y, Hayashi Y, Fukui N: Late referrals to home care service affecting death at home in advanced cancer patients in Japan: a nationwide survey. Ann Oncol. 2011, 22: 2113-2120. 10.1093/annonc/mdq719.CrossRefPubMed
32.
go back to reference Bala M, Strzeszynski L, Cahill K: Mass media interventions for smoking cessation in adults. Cochrane Database Syst Rev. 2008, CD004704-1 Bala M, Strzeszynski L, Cahill K: Mass media interventions for smoking cessation in adults. Cochrane Database Syst Rev. 2008, CD004704-1
33.
go back to reference Morita T, Miyashita M, Shibagaki M, Hirai K, Ashiya T, Ishihara T, Matsubara T, Miyoshi I, Nakaho T, Nakashima N, Onishi H, Ozawa T, Suenaga K, Tajima T, Akechi T, Uchitomi Y: Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: a population-based survey in Japan. J Pain Symptom Manage. 2006, 31: 306-316. 10.1016/j.jpainsymman.2005.09.004.CrossRefPubMed Morita T, Miyashita M, Shibagaki M, Hirai K, Ashiya T, Ishihara T, Matsubara T, Miyoshi I, Nakaho T, Nakashima N, Onishi H, Ozawa T, Suenaga K, Tajima T, Akechi T, Uchitomi Y: Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: a population-based survey in Japan. J Pain Symptom Manage. 2006, 31: 306-316. 10.1016/j.jpainsymman.2005.09.004.CrossRefPubMed
34.
go back to reference Higginson IJ, Finlay IG, Goodwin DM, Hood K, Edwards AG, Cook A, Douglas HR, Normand CE: Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers?. J Pain Symptom Manage. 2003, 25: 150-168. 10.1016/S0885-3924(02)00599-7.CrossRefPubMed Higginson IJ, Finlay IG, Goodwin DM, Hood K, Edwards AG, Cook A, Douglas HR, Normand CE: Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers?. J Pain Symptom Manage. 2003, 25: 150-168. 10.1016/S0885-3924(02)00599-7.CrossRefPubMed
35.
go back to reference Miyashita M, Morita T, Hirai K: Evaluation of end-of-life cancer care from the perspective of bereaved family members: the Japanese experience. J Clin Oncol. 2008, 26: 3845-3852. 10.1200/JCO.2007.15.8287.CrossRefPubMed Miyashita M, Morita T, Hirai K: Evaluation of end-of-life cancer care from the perspective of bereaved family members: the Japanese experience. J Clin Oncol. 2008, 26: 3845-3852. 10.1200/JCO.2007.15.8287.CrossRefPubMed
36.
go back to reference Casarett D, Karlawish J, Morales K, Crowley R, Mirsch T, Asch DA: Improving the use of hospice services in nursing homes: a randomized controlled trial. JAMA. 2005, 294: 211-217. 10.1001/jama.294.2.211.CrossRefPubMed Casarett D, Karlawish J, Morales K, Crowley R, Mirsch T, Asch DA: Improving the use of hospice services in nursing homes: a randomized controlled trial. JAMA. 2005, 294: 211-217. 10.1001/jama.294.2.211.CrossRefPubMed
37.
go back to reference Morita T, Hirai K, Sakaguchi Y, Maeyama E, Tsuneto S, Shima Y: Measuring the quality of structure and process in end-of-life care from the bereaved family perspective. J Pain Symptom Manage. 2004, 27: 492-501. 10.1016/j.jpainsymman.2003.10.014.CrossRefPubMed Morita T, Hirai K, Sakaguchi Y, Maeyama E, Tsuneto S, Shima Y: Measuring the quality of structure and process in end-of-life care from the bereaved family perspective. J Pain Symptom Manage. 2004, 27: 492-501. 10.1016/j.jpainsymman.2003.10.014.CrossRefPubMed
38.
go back to reference Miyashita M, Wada M, Morita T, Matoba M, Tsuneto S, Shima Y: Reliability and Validity of the Care Evaluation Scale patient version. Proceedings of the 15th congress of Japanese Society of Palliative Medicine, Tokyo. 2010, 165. Miyashita M, Wada M, Morita T, Matoba M, Tsuneto S, Shima Y: Reliability and Validity of the Care Evaluation Scale patient version. Proceedings of the 15th congress of Japanese Society of Palliative Medicine, Tokyo. 2010, 165.
39.
go back to reference Miyashita M, Morita T, Sato K, Shima Y, Uchitomi Y: Good Death Inventory: A measure for evaluating good death from the bereaved family member's perspective. J Pain Symptom Manage. 2008, 35: 486-498. 10.1016/j.jpainsymman.2007.07.009.CrossRefPubMed Miyashita M, Morita T, Sato K, Shima Y, Uchitomi Y: Good Death Inventory: A measure for evaluating good death from the bereaved family member's perspective. J Pain Symptom Manage. 2008, 35: 486-498. 10.1016/j.jpainsymman.2007.07.009.CrossRefPubMed
40.
go back to reference Miyashita M, Wada M, Morita T, Matoba M, Tsuneto S, Shima Y: Reliability and Validity of the Good Death Inventory patient version. Proceedings of the 15th congress of Japanese Society of Palliative Medicine, Tokyo. 2010, 165. Miyashita M, Wada M, Morita T, Matoba M, Tsuneto S, Shima Y: Reliability and Validity of the Good Death Inventory patient version. Proceedings of the 15th congress of Japanese Society of Palliative Medicine, Tokyo. 2010, 165.
41.
go back to reference Hirai K, Miyashita M, Morita T, Sanjo M, Uchitomi Y: Good death in Japanese cancer care: a qualitative study. J Pain Symptom Manage. 2006, 31: 140-147. 10.1016/j.jpainsymman.2005.06.012.CrossRefPubMed Hirai K, Miyashita M, Morita T, Sanjo M, Uchitomi Y: Good death in Japanese cancer care: a qualitative study. J Pain Symptom Manage. 2006, 31: 140-147. 10.1016/j.jpainsymman.2005.06.012.CrossRefPubMed
42.
go back to reference Miyashita M, Sanjo M, Morita T, Hirai K, Uchitomi Y: Good death in cancer care: a nationwide quantitative study. Ann Oncol. 2007, 18: 1090-1097. 10.1093/annonc/mdm068.CrossRefPubMed Miyashita M, Sanjo M, Morita T, Hirai K, Uchitomi Y: Good death in cancer care: a nationwide quantitative study. Ann Oncol. 2007, 18: 1090-1097. 10.1093/annonc/mdm068.CrossRefPubMed
43.
go back to reference Uki J, Mendoza T, Cleeland CS, Nakamura Y, Takeda F: A brief cancer pain assessment tool in Japanese: the utility of the Japanese Brief Pain Inventory--BPI-J. J Pain Symptom Manage. 1998, 16: 364-373. 10.1016/S0885-3924(98)00098-0.CrossRefPubMed Uki J, Mendoza T, Cleeland CS, Nakamura Y, Takeda F: A brief cancer pain assessment tool in Japanese: the utility of the Japanese Brief Pain Inventory--BPI-J. J Pain Symptom Manage. 1998, 16: 364-373. 10.1016/S0885-3924(98)00098-0.CrossRefPubMed
44.
go back to reference Igarashi A, Miyashita M, Morita T, Akizuki N, Akiyama M, Shirahige Y, Eguchi K: A scale for measuring feelings of support and security about cancer care in a region of Japan: a potential new endpoint of palliative care. J Pain Symptom Manage. 2011. Igarashi A, Miyashita M, Morita T, Akizuki N, Akiyama M, Shirahige Y, Eguchi K: A scale for measuring feelings of support and security about cancer care in a region of Japan: a potential new endpoint of palliative care. J Pain Symptom Manage. 2011.
45.
go back to reference Sanjo M, Morita T, Miyashita M, Shiozaki M, Sato K, Hirai K, Shima Y, Uchitomi Y: Caregiving Consequences Inventory: a measure for evaluating caregiving consequences from the bereaved family member's perspective. Psychooncology. 2009, 18: 657-666. 10.1002/pon.1447.CrossRefPubMed Sanjo M, Morita T, Miyashita M, Shiozaki M, Sato K, Hirai K, Shima Y, Uchitomi Y: Caregiving Consequences Inventory: a measure for evaluating caregiving consequences from the bereaved family member's perspective. Psychooncology. 2009, 18: 657-666. 10.1002/pon.1447.CrossRefPubMed
46.
go back to reference Nakazawa Y, Miyashita M, Morita T, Umeda M, Oyagi Y, Ogasawara T: The palliative care knowledge test: reliability and validity of an instrument to measure palliative care knowledge among health professionals. Palliat Med. 2009, 23: 754-766. 10.1177/0269216309106871.CrossRefPubMed Nakazawa Y, Miyashita M, Morita T, Umeda M, Oyagi Y, Ogasawara T: The palliative care knowledge test: reliability and validity of an instrument to measure palliative care knowledge among health professionals. Palliat Med. 2009, 23: 754-766. 10.1177/0269216309106871.CrossRefPubMed
47.
go back to reference Nakazawa Y, Miyashita M, Morita T, Umeda M, Oyagi Y, Ogasawara T: The palliative care self-reported practices scale and the palliative care difficulties scale: reliability and validity of two scales evaluating self-reported practices and difficulties experienced in palliative care by health professionals. J Palliat Med. 2010, 13: 427-437. 10.1089/jpm.2009.0289.CrossRefPubMed Nakazawa Y, Miyashita M, Morita T, Umeda M, Oyagi Y, Ogasawara T: The palliative care self-reported practices scale and the palliative care difficulties scale: reliability and validity of two scales evaluating self-reported practices and difficulties experienced in palliative care by health professionals. J Palliat Med. 2010, 13: 427-437. 10.1089/jpm.2009.0289.CrossRefPubMed
Metadata
Title
A region-based palliative care intervention trial using the mixed-method approach: Japan OPTIM study
Authors
Tatsuya Morita
Mitsunori Miyashita
Akemi Yamagishi
Nobuya Akizuki
Yoshiyuki Kizawa
Yutaka Shirahige
Miki Akiyama
Kei Hirai
Motohiro Matoba
Masako Yamada
Taketoshi Matsumoto
Takuhiro Yamaguchi
Kenji Eguchi
Publication date
01-12-2012
Publisher
BioMed Central
Published in
BMC Palliative Care / Issue 1/2012
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/1472-684X-11-2

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