ERANet-LAC CODE: International Care Of the Dying Evaluation
NCT ID: NCT03566732
Last Updated: 2023-08-28
Study Results
Results available
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
Recruitment Status
COMPLETED
Total Enrollment
914 participants
Study Classification
OBSERVATIONAL
Study Start Date
2017-08-15
Study Completion Date
2018-12-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Providing high quality care for dying patients and their families is very important. One way one can assess the care provided is to ask bereaved relatives to complete a questionnaire after their family member has died. The questionnaire can ask about their experiences and their thoughts about the care provided to their family member.
One such questionnaire is the 'Care Of the Dying Evaluation' (or CODE). CODE has been developed with the help and support of bereaved relatives and has been used extensively within the United Kingdom. In this project the investigators want to use the CODE questionnaire to look at bereaved relatives' views about care provided in seven different countries within Europe and Latin America. In the first part of the project CODE was translated into the main language of each country. Volunteers and bereaved relatives in each country were asked to give feedback about whether CODE was easy to understand, sensitive, and easy to complete. Based on the feedback a common version of CODE that is suitable for use across all the countries was developed.
In the next phase of the project, relatives who have recently experienced a bereavement where one of their family members has died from cancer in a hospital, will be invited to complete the CODE questionnaire about two months after the patient's death. The relatives may complete CODE on paper, using a computer, or by interview. The aim is to have 100 completed CODE questionnaires from each of the seven countries. The data from the questionnaires will be used to make a report on the current quality of care for dying cancer patients in hospitals across the seven countries. It will also be possible to compare the care between the countries and identify areas needing improvement.
In the next phase of the project, health care professionals, researchers and bereaved relatives together will use their knowledge and experience to find effective ways to improve the weak areas identified, and assess the results of putting these changes into practice.
One such questionnaire is the 'Care Of the Dying Evaluation' (or CODE). CODE has been developed with the help and support of bereaved relatives and has been used extensively within the United Kingdom. In this project the investigators want to use the CODE questionnaire to look at bereaved relatives' views about care provided in seven different countries within Europe and Latin America. In the first part of the project CODE was translated into the main language of each country. Volunteers and bereaved relatives in each country were asked to give feedback about whether CODE was easy to understand, sensitive, and easy to complete. Based on the feedback a common version of CODE that is suitable for use across all the countries was developed.
In the next phase of the project, relatives who have recently experienced a bereavement where one of their family members has died from cancer in a hospital, will be invited to complete the CODE questionnaire about two months after the patient's death. The relatives may complete CODE on paper, using a computer, or by interview. The aim is to have 100 completed CODE questionnaires from each of the seven countries. The data from the questionnaires will be used to make a report on the current quality of care for dying cancer patients in hospitals across the seven countries. It will also be possible to compare the care between the countries and identify areas needing improvement.
In the next phase of the project, health care professionals, researchers and bereaved relatives together will use their knowledge and experience to find effective ways to improve the weak areas identified, and assess the results of putting these changes into practice.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Validation of the European Oncology Quality of Life Toolkit
NCT05947903
Cancer
Survivorship
Palliative Care
NOT_YET_RECRUITING
Family and Coping Oriented Palliative Homecare Nursing Aimed at Advanced Cancer Patients
NCT01444157
Advanced Cancer
COMPLETED
PHASE3
Palliative Outcome Evaluation Muenster I
NCT03286127
Cancer
Chronic Heart Failure
COPD Exacerbation
+1 more
UNKNOWN
Cancer End Of Life Evaluation
NCT01545921
Advanced Cancer
TERMINATED
NA
Impact of a Booklet-Question List on Cancer Patients or Their Families Seeking Prognostic Information During a Palliative Care Consultation
NCT02854293
Metastatic Cancer
Palliative Care
COMPLETED
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
ABSTRACT
Background: In order to ensure the highest quality of care is provided for dying patients and their families, one needs to first be able to robustly evaluate the current quality of care. One identified method is to assess this from the user-perspective by conducting bereaved relatives' surveys. 'Care Of the Dying Evaluation' (CODE) is a recognised, validated post-bereavement questionnaire which has been extensively used within the United Kingdom. The ERANet-LAC CODE project aims to use CODE in a wider international context. In Work Package 1 of the project, CODE will be translated and pilot tested in volunteers and bereaved relatives in the partner countries. Using a consensus procedure, a final version of the international CODE (i-CODE) questionnaire will be developed.
Aims: The present project (Work Package 2) aims to advance the international evidence in care for dying cancer patients by undertaking an observational study of bereaved relatives' views across seven participating countries. The overall aims of Work Package 2 (WP2) are to:
* Conduct an international survey of bereaved relatives of cancer patients dying in hospitals, using the CODE questionnaire
* Use the CODE data to provide feedback about the quality of care and level of family support at an international and national level, allowing for cross-country comparisons
* Conduct a web survey of all participating institutions to be able to interpret the survey data in the context of information about each organisation and the level of specialist palliative care provision at each site / country
Methods: Bereaved adult relatives, to adult cancer patients who had an 'expected' death in hospital, will be approached face to face, by telephone or in writing and invited to complete the CODE questionnaire. The CODE questionnaire pack will be sent out 6-8 weeks after bereavement. CODE may be completed via self-completion paper questionnaire, via on-line questionnaire, or facilitated via a researcher using a tablet, telephone or face-to-face interview, according to what is feasible and acceptable in each country. The aim is 100 completed questionnaires per country. Basic demographics will be recorded for all potential participants and for the patients who died.
Analysis of results: Data will be analysed using SPSS and according to the CODE user guide, to present a common international report, individual country reports and cross-country comparisons. Data will be interpreted in the context of knowledge about the individual sites/countries.
Conclusions: The expected outcomes from WP2 are an international survey and cross-country comparisons about the current quality of care for dying cancer patients as perceived by bereaved people, including key areas where care needs to be improved. WP3 of the project will use the results of the international survey to implement changes to improve the care.
INTRODUCTION
The present project was proposed in response to the ERANet-LAC 2nd Joint Call on Research and Innovation and approved for funding under the European Commission's 7th framework program. The aim of the project is to inform and develop an evidence based approach to systematically standardize assessment and care of dying cancer patients, using relative generated outcomes. The project will be conducted in four European and three South American countries three years starting from January 2017. The project contains three Work Packages (parts). This protocol describes the work to be undertaken in Work Package 2 (CODE International Survey).
BACKGROUND
The delivery of appropriate care for dying cancer patients remains a key medical, social, economic and political issue. However, the quality of care for the dying is diverse both within and between EU-LAC countries.
Based on the international evidence base, a set of core principles for care of the dying has been defined. These principles are applicable to the care of dying cancer patients, as well as other patients, worldwide.
In order to ensure the highest quality of care provisions, one needs to first be able to robustly evaluate the current quality of care. One method is to assess this from the user-perspective by conducting bereaved relatives' surveys.
'Care Of the Dying Evaluation' Questionnaire
One post-bereavement questionnaire is 'Care Of the Dying Evaluation' (CODE). This is a 42-item self-completion questionnaire, developed within the UK, and focused on the quality of care and the level of support provided to individuals and their families in the last days of life and the immediate post-bereavement period.
CODE has been used and validated with bereaved relatives, including undertaking cognitive 'think aloud' interviews to assess face and content validity; assessing CODE's stability over time by conducting test-retest reliability analysis; and assessing the construct validity and internal consistency of CODE. Subsequently, CODE has been used across hospices, hospitals and community settings.
In Work Package 1 of the present project, CODE was translated from English into the main language of each partner country according to established international procedures, and pilot tested in volunteers and bereaved relatives to assure understanding and appropriate cultural adaptation. Based on feedback from the testing in each country, a common, international version of CODE (iCODE) has been established through a consensus procedure.
AIMS \& OBJECTIVES
The present project (Work Package 2) aims to advance the international evidence in care for dying patients by undertaking an observational study of bereaved relatives' views across seven participating countries, by use of the CODE questionnaire.
The overall aims of Work Package 2 (WP2) are:
* Conduct an international survey of bereaved relatives of cancer patients dying in hospitals, using the CODE questionnaire
* Conduct a web survey of all participating institutions to aid in the interpretation of the survey data
* Use the CODE data to provide feedback about the quality of care and level of family support at an international and national level, allowing for cross-country comparisons
METHODS
Study sites
The necessary number of hospitals caring for adult cancer patients will be recruited as study sites. The study will only be performed in institutions defined as hospitals
Recruitment
The relative / next-of-kin must be approached after the patient's death. The investigators will approach the person recorded as next-of-kin in the patient's hospital record.
Only one completed questionnaire will be included per deceased patient.
Recruitment will be done prospectively. The method of recruitment will be adapted as to what is feasible and in the individual country.
DATA COLLECTION
CODE International Survey
Data to be collected The CODE questionnaire is the common data collection tool of the study. CODE also includes demographic data. Information about the hospital stay will be included for all cases, as part of the inclusion procedure.
Method of data collection
The CODE questionnaire will be sent to the participants 6-8 weeks post bereavement, with on reminder. CODE International Survey was intended as a postal survey, but other data collection methods will also be accepted.
Sample estimation:
Minimum acceptable number of questionnaires per country is 100 (with this number, a 95% confidence interval will give a margin of error of +/- 10% of the primary outcome).
Data transfer
The electronic version and database for CODE for each country/language will be developed in Norway using the Corporate Surveyor software. The databases will be merged in Norway for the final common analyses.
A web survey of study sites will also be conducted.
DATA ANALYSIS
Data will be analysed using the R statistical package, using descriptive statistics (proportions (%) for categorical data; means and standard deviations for continuous parametric data and medians and interquartile range for continuous non-parametric data).
The dataset, anonymised at patient, site and country level, will be aggregated at international level to enable an international report. Results will be summarised in tabular and graphical format, as appropriate.
Free text comments will be analysed using qualitative methods (text condensation).
PROJECT MANAGEMENT AND WORK PLAN
All partners have signed the consortium agreement. The PIs are responsible for the CODE international survey in their respective countries. The group of PIs constitute the project General Assembly and decision-making body.
WP1 (Preparation and Piloting) ran from month 1 to month 7 of the project, i.e. from January to August 2017.
WP2 is designed to run from month 8 to month 22 of the project, i.e. from September 2017 to November 2018.
Time line and deliverables
Confirmation of ethical approval for CODE International Survey in each country: month 6 (July 2017) Web survey of institutions ready for use: month 6 (July 2017) Fully developed, tested and web-accessible data collection tools: month 6 (July 2017) i-CODE ready for use: month 7 (Aug 2017) Completed web survey of inclusion sites: month 10 (Nov 2017) Completed international survey with at least 600 completed CODE questionnaires: month 22 (Nov 2018) Report on CODE International Survey data: month 22 (Nov 2018)
SPONSORSHIP AND BUDGET
Financial support for the project was granted from national research funding agencies in the participating countries, except in the UK. The University of Liverpool, UK, takes part in the project as self-financed partner.
No commercial interests are involved in the study. No conflicts of interest have been declared. Participants receive no financial benefit for participation.
ETHICAL APPROVAL AND GOVERNANCE
The Project Lead (PI) for each country will seek the necessary approvals for CODE International Survey, from their local/regional ethics committee, and from their institutional review board as needed. All countries will need ethical approval for WP2.
All potential participants will be given a Participant Information Sheet detailing the aims of the study and informing that participation is fully voluntary.
PATIENT AND PUBLIC INVOLVEMENT Both volunteers and bereaved relatives will be deeply involved in developing i-CODE to be used for the international survey.
After the survey has been performed, bereaved relatives will be involved in the action planning on how to address the main areas of concern identified.
CONFIDENTIALITY AND DATA MANAGEMENT
The Project Lead for each country will preserve the confidentiality of participants taking part in the study. All data will be anonymised and individual participants will not be identifiable from published data.
All data will be stored on a secure, password protected research server. Data will be stored for up to five years after the completion of the project before being confidentially shredded or deleted.
DISSEMINATION AND PUBLICATIONS
A website for the project will be established.
Authorship will be defined according to the Vancouver Guidelines. National data may be published by the study group in each country.
The last project meeting with presentations and discussions of the project findings will be arranged as an open international conference.
Background: In order to ensure the highest quality of care is provided for dying patients and their families, one needs to first be able to robustly evaluate the current quality of care. One identified method is to assess this from the user-perspective by conducting bereaved relatives' surveys. 'Care Of the Dying Evaluation' (CODE) is a recognised, validated post-bereavement questionnaire which has been extensively used within the United Kingdom. The ERANet-LAC CODE project aims to use CODE in a wider international context. In Work Package 1 of the project, CODE will be translated and pilot tested in volunteers and bereaved relatives in the partner countries. Using a consensus procedure, a final version of the international CODE (i-CODE) questionnaire will be developed.
Aims: The present project (Work Package 2) aims to advance the international evidence in care for dying cancer patients by undertaking an observational study of bereaved relatives' views across seven participating countries. The overall aims of Work Package 2 (WP2) are to:
* Conduct an international survey of bereaved relatives of cancer patients dying in hospitals, using the CODE questionnaire
* Use the CODE data to provide feedback about the quality of care and level of family support at an international and national level, allowing for cross-country comparisons
* Conduct a web survey of all participating institutions to be able to interpret the survey data in the context of information about each organisation and the level of specialist palliative care provision at each site / country
Methods: Bereaved adult relatives, to adult cancer patients who had an 'expected' death in hospital, will be approached face to face, by telephone or in writing and invited to complete the CODE questionnaire. The CODE questionnaire pack will be sent out 6-8 weeks after bereavement. CODE may be completed via self-completion paper questionnaire, via on-line questionnaire, or facilitated via a researcher using a tablet, telephone or face-to-face interview, according to what is feasible and acceptable in each country. The aim is 100 completed questionnaires per country. Basic demographics will be recorded for all potential participants and for the patients who died.
Analysis of results: Data will be analysed using SPSS and according to the CODE user guide, to present a common international report, individual country reports and cross-country comparisons. Data will be interpreted in the context of knowledge about the individual sites/countries.
Conclusions: The expected outcomes from WP2 are an international survey and cross-country comparisons about the current quality of care for dying cancer patients as perceived by bereaved people, including key areas where care needs to be improved. WP3 of the project will use the results of the international survey to implement changes to improve the care.
INTRODUCTION
The present project was proposed in response to the ERANet-LAC 2nd Joint Call on Research and Innovation and approved for funding under the European Commission's 7th framework program. The aim of the project is to inform and develop an evidence based approach to systematically standardize assessment and care of dying cancer patients, using relative generated outcomes. The project will be conducted in four European and three South American countries three years starting from January 2017. The project contains three Work Packages (parts). This protocol describes the work to be undertaken in Work Package 2 (CODE International Survey).
BACKGROUND
The delivery of appropriate care for dying cancer patients remains a key medical, social, economic and political issue. However, the quality of care for the dying is diverse both within and between EU-LAC countries.
Based on the international evidence base, a set of core principles for care of the dying has been defined. These principles are applicable to the care of dying cancer patients, as well as other patients, worldwide.
In order to ensure the highest quality of care provisions, one needs to first be able to robustly evaluate the current quality of care. One method is to assess this from the user-perspective by conducting bereaved relatives' surveys.
'Care Of the Dying Evaluation' Questionnaire
One post-bereavement questionnaire is 'Care Of the Dying Evaluation' (CODE). This is a 42-item self-completion questionnaire, developed within the UK, and focused on the quality of care and the level of support provided to individuals and their families in the last days of life and the immediate post-bereavement period.
CODE has been used and validated with bereaved relatives, including undertaking cognitive 'think aloud' interviews to assess face and content validity; assessing CODE's stability over time by conducting test-retest reliability analysis; and assessing the construct validity and internal consistency of CODE. Subsequently, CODE has been used across hospices, hospitals and community settings.
In Work Package 1 of the present project, CODE was translated from English into the main language of each partner country according to established international procedures, and pilot tested in volunteers and bereaved relatives to assure understanding and appropriate cultural adaptation. Based on feedback from the testing in each country, a common, international version of CODE (iCODE) has been established through a consensus procedure.
AIMS \& OBJECTIVES
The present project (Work Package 2) aims to advance the international evidence in care for dying patients by undertaking an observational study of bereaved relatives' views across seven participating countries, by use of the CODE questionnaire.
The overall aims of Work Package 2 (WP2) are:
* Conduct an international survey of bereaved relatives of cancer patients dying in hospitals, using the CODE questionnaire
* Conduct a web survey of all participating institutions to aid in the interpretation of the survey data
* Use the CODE data to provide feedback about the quality of care and level of family support at an international and national level, allowing for cross-country comparisons
METHODS
Study sites
The necessary number of hospitals caring for adult cancer patients will be recruited as study sites. The study will only be performed in institutions defined as hospitals
Recruitment
The relative / next-of-kin must be approached after the patient's death. The investigators will approach the person recorded as next-of-kin in the patient's hospital record.
Only one completed questionnaire will be included per deceased patient.
Recruitment will be done prospectively. The method of recruitment will be adapted as to what is feasible and in the individual country.
DATA COLLECTION
CODE International Survey
Data to be collected The CODE questionnaire is the common data collection tool of the study. CODE also includes demographic data. Information about the hospital stay will be included for all cases, as part of the inclusion procedure.
Method of data collection
The CODE questionnaire will be sent to the participants 6-8 weeks post bereavement, with on reminder. CODE International Survey was intended as a postal survey, but other data collection methods will also be accepted.
Sample estimation:
Minimum acceptable number of questionnaires per country is 100 (with this number, a 95% confidence interval will give a margin of error of +/- 10% of the primary outcome).
Data transfer
The electronic version and database for CODE for each country/language will be developed in Norway using the Corporate Surveyor software. The databases will be merged in Norway for the final common analyses.
A web survey of study sites will also be conducted.
DATA ANALYSIS
Data will be analysed using the R statistical package, using descriptive statistics (proportions (%) for categorical data; means and standard deviations for continuous parametric data and medians and interquartile range for continuous non-parametric data).
The dataset, anonymised at patient, site and country level, will be aggregated at international level to enable an international report. Results will be summarised in tabular and graphical format, as appropriate.
Free text comments will be analysed using qualitative methods (text condensation).
PROJECT MANAGEMENT AND WORK PLAN
All partners have signed the consortium agreement. The PIs are responsible for the CODE international survey in their respective countries. The group of PIs constitute the project General Assembly and decision-making body.
WP1 (Preparation and Piloting) ran from month 1 to month 7 of the project, i.e. from January to August 2017.
WP2 is designed to run from month 8 to month 22 of the project, i.e. from September 2017 to November 2018.
Time line and deliverables
Confirmation of ethical approval for CODE International Survey in each country: month 6 (July 2017) Web survey of institutions ready for use: month 6 (July 2017) Fully developed, tested and web-accessible data collection tools: month 6 (July 2017) i-CODE ready for use: month 7 (Aug 2017) Completed web survey of inclusion sites: month 10 (Nov 2017) Completed international survey with at least 600 completed CODE questionnaires: month 22 (Nov 2018) Report on CODE International Survey data: month 22 (Nov 2018)
SPONSORSHIP AND BUDGET
Financial support for the project was granted from national research funding agencies in the participating countries, except in the UK. The University of Liverpool, UK, takes part in the project as self-financed partner.
No commercial interests are involved in the study. No conflicts of interest have been declared. Participants receive no financial benefit for participation.
ETHICAL APPROVAL AND GOVERNANCE
The Project Lead (PI) for each country will seek the necessary approvals for CODE International Survey, from their local/regional ethics committee, and from their institutional review board as needed. All countries will need ethical approval for WP2.
All potential participants will be given a Participant Information Sheet detailing the aims of the study and informing that participation is fully voluntary.
PATIENT AND PUBLIC INVOLVEMENT Both volunteers and bereaved relatives will be deeply involved in developing i-CODE to be used for the international survey.
After the survey has been performed, bereaved relatives will be involved in the action planning on how to address the main areas of concern identified.
CONFIDENTIALITY AND DATA MANAGEMENT
The Project Lead for each country will preserve the confidentiality of participants taking part in the study. All data will be anonymised and individual participants will not be identifiable from published data.
All data will be stored on a secure, password protected research server. Data will be stored for up to five years after the completion of the project before being confidentially shredded or deleted.
DISSEMINATION AND PUBLICATIONS
A website for the project will be established.
Authorship will be defined according to the Vancouver Guidelines. National data may be published by the study group in each country.
The last project meeting with presentations and discussions of the project findings will be arranged as an open international conference.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Neoplasms
Bereavement
Quality of Life
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
Observational Model Type
CASE_ONLY
Study Time Perspective
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Bereaved relatives
Bereaved relatives after cancer deaths in hospitals
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Next-of-kin to a patient who died an 'expected' death from cancer in hospital
* Has been present at the hospital together with the patient at least some of the time during the patient's last two days. (This might not always be known or recorded, therefore the participant may have the option to pass the questionnaire on to somebody better placed to complete it.)
* Patient was ≥ 18 years of age at the time of Death
* Patient had been admitted to the hospital (not any specific ward) at least three calendar days (e.g., admission August 1st, died August 3rd)
* Able to give written informed consent, which might be implied when the participant completes and returns the questionnaire, in keeping with the ethical stipulations for each country
* Has been present at the hospital together with the patient at least some of the time during the patient's last two days. (This might not always be known or recorded, therefore the participant may have the option to pass the questionnaire on to somebody better placed to complete it.)
* Patient was ≥ 18 years of age at the time of Death
* Patient had been admitted to the hospital (not any specific ward) at least three calendar days (e.g., admission August 1st, died August 3rd)
* Able to give written informed consent, which might be implied when the participant completes and returns the questionnaire, in keeping with the ethical stipulations for each country
Exclusion Criteria
* Patient had a sudden and unexpected death
* Unable to complete the questionnaire due to language abilities or reduced cognitive functioning (in some countries the offer of a translator would be provided if someone wanted to complete the questionnaire but had difficulty due to languages)
* Unable to complete the questionnaire due to language abilities or reduced cognitive functioning (in some countries the offer of a translator would be provided if someone wanted to complete the questionnaire but had difficulty due to languages)
Minimum Eligible Age
18 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sue Ryder House
OTHER
Sponsor Role
collaborator
Mutualista Asociación Hospital Evangélico
OTHER
Sponsor Role
collaborator
Pallium Latinoamérica N.G.O
OTHER
Sponsor Role
collaborator
University Medical Center Mainz
OTHER
Sponsor Role
collaborator
University of Campinas, Brazil
OTHER
Sponsor Role
collaborator
University of Liverpool
OTHER
Sponsor Role
collaborator
University of Bergen
OTHER
Sponsor Role
lead
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Responsibility Role
SPONSOR
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Dagny F. Haugen, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Bergen
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital Carlos B. Udaondo
Buenos Aires, , Argentina
Site Status
Instituto de Investigaciones Médicas Alfredo Lanari. Universidad de Buenos Aires
Buenos Aires, , Argentina
Site Status
Hospital Universitario Privado de Córdoba
Córdoba, , Argentina
Site Status
Sumare State Hospital
São Paulo, , Brazil
Site Status
Katholisches Klinikum Mainz
Mainz, , Germany
Site Status
University Medical Centre of the Johannes Gutenberg University of Mainz
Mainz, , Germany
Site Status
Haukeland University Hospital
Bergen, , Norway
Site Status
Haraldsplass Deaconal Hospital
Bergen, , Norway
Site Status
Bærum Hospital, Vestre Viken
Bærum, , Norway
Site Status
Førde Central Hospital
Førde, , Norway
Site Status
Haugesund Hospital
Haugesund, , Norway
Site Status
Stavanger University Hospital
Stavanger, , Norway
Site Status
St Olavs Hospital
Trondheim, , Norway
Site Status
Pulmonological Hospital in Bydgoszcz
Bydgoszcz, , Poland
Site Status
D. Wladyslaw Biegański Regional Specialist Hospital
Grudziądz, , Poland
Site Status
F. Dłutek Autonomic Public Healthcare Centre
Rypin, , Poland
Site Status
Provincial Specialist Hospital in name of the blessed priest Popiełuszko
Włocławek, , Poland
Site Status
Paluckie Health Centre, Żnin Hospital
Żnin, , Poland
Site Status
Royal Liverpool University Hospital
Liverpool, , United Kingdom
Site Status
Mutualista Asociación Hospital Evangélico
Montevideo, , Uruguay
Site Status
Countries
Review the countries where the study has at least one active or historical site.
Argentina
Brazil
Germany
Norway
Poland
United Kingdom
Uruguay
References
Explore related publications, articles, or registry entries linked to this study.
Mayland CR, Mulholland H, Gambles M, Ellershaw J, Stewart K. How well do we currently care for our dying patients in acute hospitals: the views of the bereaved relatives? BMJ Support Palliat Care. 2017 Sep;7(3):316-325. doi: 10.1136/bmjspcare-2014-000810. Epub 2017 Jan 17.
Reference Type
BACKGROUND
Quality Assurance for Care of the Dying: Cheshire & Merseyside Strategic Clinical Network. Network Report. October 2015.
Reference Type
BACKGROUND
Stiel S, Heckel M, Bussmann S, Weber M, Ostgathe C. End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation study. BMC Palliat Care. 2015 May 2;14:21. doi: 10.1186/s12904-015-0020-4.
Reference Type
BACKGROUND
Malterud K. Systematic text condensation: a strategy for qualitative analysis. Scand J Public Health. 2012 Dec;40(8):795-805. doi: 10.1177/1403494812465030.
Reference Type
BACKGROUND
Germain A, Mayland CR, Jack BA. The potential therapeutic value for bereaved relatives participating in research: An exploratory study. Palliat Support Care. 2016 Oct;14(5):479-87. doi: 10.1017/S1478951515001194. Epub 2015 Oct 29.
Reference Type
BACKGROUND
Mayland CR, Gerlach C, Sigurdardottir K, Hansen MIT, Leppert W, Stachowiak A, Krajewska M, Garcia-Yanneo E, Tripodoro VA, Goldraij G, Weber M, Zambon L, Passarini JN, Saad IB, Ellershaw J, Haugen DF. Assessing quality of care for the dying from the bereaved relatives' perspective: Using pre-testing survey methods across seven countries to develop an international outcome measure. Palliat Med. 2019 Mar;33(3):357-368. doi: 10.1177/0269216318818299. Epub 2019 Jan 10.
Reference Type
RESULT
Hansen MIT, Haugen DF, Sigurdardottir KR, Kvikstad A, Mayland CR, Schaufel MA; ERANet-LAC CODE project group. Factors affecting quality of end-of-life hospital care - a qualitative analysis of free text comments from the i-CODE survey in Norway. BMC Palliat Care. 2020 Jul 7;19(1):98. doi: 10.1186/s12904-020-00609-x.
Reference Type
RESULT
Haugen DF, Hufthammer KO, Gerlach C, Sigurdardottir K, Hansen MIT, Ting G, Tripodoro VA, Goldraij G, Yanneo EG, Leppert W, Wolszczak K, Zambon L, Passarini JN, Saad IAB, Weber M, Ellershaw J, Mayland CR; ERANet-LAC CODE Project Group. Good Quality Care for Cancer Patients Dying in Hospitals, but Information Needs Unmet: Bereaved Relatives' Survey within Seven Countries. Oncologist. 2021 Jul;26(7):e1273-e1284. doi: 10.1002/onco.13837. Epub 2021 Jun 17.
Reference Type
RESULT
Goldraij G, Tripodoro VA, Aloisio M, Castro SA, Gerlach C, Mayland CR, Haugen DF; ERANet-LAC CODE Project Group; ERANet-LAC CODE project group. One chance to get it right: improving clinical handovers for better symptom control at the end of life. BMJ Open Qual. 2021 Sep;10(3):e001436. doi: 10.1136/bmjoq-2021-001436.
Reference Type
RESULT
Hjorth NE, Hufthammer KO, Sigurdardottir K, Tripodoro VA, Goldraij G, Kvikstad A, Haugen DF; ERANet-LAC CODE project group; Core scientific group. Hospital care for the dying patient with cancer: does an advance care planning invitation influence bereaved relatives' experiences? A two country survey. BMJ Support Palliat Care. 2024 Jan 8;13(e3):e1038-e1047. doi: 10.1136/bmjspcare-2021-003116.
Reference Type
RESULT
Mayland CR, Keetharuth AD, Mukuria C, Haugen DF. Validation of 'Care Of the Dying Evaluation' (CODETM) within an international study exploring bereaved relatives' perceptions about quality of care in the last days of life. J Pain Symptom Manage. 2022 Jul;64(1):e23-e33. doi: 10.1016/j.jpainsymman.2022.02.340. Epub 2022 Mar 5.
Reference Type
RESULT
Gerlach C, Baus M, Gianicolo E, Bayer O, Haugen DF, Weber M, Mayland CR; ERANet-LAC CODE Core scientific group. What do bereaved relatives of cancer patients dying in hospital want to tell us? Analysis of free-text comments from the International Care of the Dying Evaluation (i-CODE) survey: a mixed methods approach. Support Care Cancer. 2022 Dec 23;31(1):81. doi: 10.1007/s00520-022-07490-9.
Reference Type
RESULT
The 2015 Quality of Death index. Ranking palliative care across the world. The Economist Intelligence Unit. A report by The Economist Intelligence Unit. Lien Foundation 2015.
Reference Type
BACKGROUND
Pastrana T, De Lima L, Wenk R, et al. Atlas de Cuidados Paliativos de Latinoamérica. Houston,TX: IAHPC Press, 2012.
Reference Type
BACKGROUND
Pastrana T, Eisenchlas J, Centeno C, De Lima L. Status of palliative care in Latin America: looking through the Latin America Atlas of Palliative Care. Curr Opin Support Palliat Care. 2013 Dec;7(4):411-6. doi: 10.1097/SPC.0000000000000008.
Reference Type
BACKGROUND
National care of the dying audit for hospitals, England. National report, Royal College of Physicians, May 2014
Reference Type
BACKGROUND
The International Collaborative for Best Care for the Dying Person. Supporting Care in the Last Hours or Days of Life. May 2014.
Reference Type
BACKGROUND
Department of Health (2008). End of life care strategy. Promoting high quality care for all adults at the end of life. Department of Health: London.
Reference Type
BACKGROUND
Burge F, Lawson B, Johnston G, Asada Y, McIntyre PF, Grunfeld E, Flowerdew G. Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter? BMC Palliat Care. 2014 May 14;13:25. doi: 10.1186/1472-684X-13-25. eCollection 2014.
Reference Type
BACKGROUND
Office of National Statistics (2014). National Survey of Bereaved People (VOICES) 2014. Office of National Statistics.
Reference Type
BACKGROUND
van der Heide A, de Vogel-Voogt E, Visser AP, van der Rijt CC, van der Maas PJ. Dying at home or in an institution: perspectives of Dutch physicians and bereaved relatives. Support Care Cancer. 2007 Dec;15(12):1413-21. doi: 10.1007/s00520-007-0254-7. Epub 2007 Apr 20.
Reference Type
BACKGROUND
Mayland CR, Williams EM, Ellershaw JE. Assessing quality of care for the dying: the development and initial validation of a postal self-completion questionnaire for bereaved relatives. Palliat Med. 2012 Oct;26(7):897-907. doi: 10.1177/0269216311424953. Epub 2011 Nov 1.
Reference Type
BACKGROUND
Department of Health (2013) The NHS Friends and Family Test: Publication Guidelines.
Reference Type
BACKGROUND
Mayland CR, Williams EM, Addington-Hall J, Cox TF, Ellershaw JE. Does the 'Liverpool Care Pathway' facilitate an improvement in quality of care for dying cancer patients? Br J Cancer. 2013 May 28;108(10):1942-8. doi: 10.1038/bjc.2013.203. Epub 2013 May 16.
Reference Type
BACKGROUND
Mayland CR, Williams EM, Addington-Hall J, Cox TF, Ellershaw JE. Assessing the quality of care for dying patients from the bereaved relatives' perspective: further validation of "Evaluating care and health outcomes--for the dying". J Pain Symptom Manage. 2014 Apr;47(4):687-96. doi: 10.1016/j.jpainsymman.2013.05.013. Epub 2013 Nov 5.
Reference Type
BACKGROUND
Mayland C, Williams E, Ellershaw J. How well do current instruments using bereaved relatives' views evaluate care for dying patients? Palliat Med. 2008 Mar;22(2):133-44. doi: 10.1177/0269216307085742.
Reference Type
BACKGROUND
Mayland CR, Lees C, Germain A, Jack BA, Cox TF, Mason SR, West A, Ellershaw JE. Caring for those who die at home: the use and validation of 'Care Of the Dying Evaluation' (CODE) with bereaved relatives. BMJ Support Palliat Care. 2014 Jun;4(2):167-174. doi: 10.1136/bmjspcare-2013-000596. Epub 2014 Mar 28.
Reference Type
BACKGROUND
Mayland C. User-guide for 'Care of the Dying Evaluation' (CODETM). The Marie Curie Palliative Care Institute Liverpool, 2015.
Reference Type
BACKGROUND
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Related Links
Access external resources that provide additional context or updates about the study.
https://www.eucelac-platform.eu/sites/default/files/short_pdescription_2nd_joint_call_0.pdf
Short description of project, ERANet-LAC website
https://www.uib.no/sites/w3.uib.no/files/attachments/innovations_umbrella_booklet_final_0.pdf
Innovations Umbrella booklet - a collection of ideas and experiences from the ERANet-LAC CODE project
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ELAC2015/T07-0545
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.
Quality of Life and Cancers in Nursing Homes
NCT03343210
TERMINATED
NA
The Effectiveness of the LCP in Improving End of Life Care for Dying Cancer Patients in Hospital.
NCT01081899
COMPLETED
PHASE3
Elaboration of a Multi-dimensional Indicator of Quality in Palliative Care
NCT02814682
COMPLETED
Patient-centred Integrated Palliative Care Pathways in Advanced Cancer and Chronic Disease
NCT02175147
UNKNOWN
Which Health-care Professional(s) to Talk About Advance Care Planning ?
NCT06376799
RECRUITING
Evaluation of End of Life Quality of Care
NCT03775304
COMPLETED
Quality of Life Assessment for Early Identification of Supportive Care Needs in Oncology Patients
NCT06337487
NOT_YET_RECRUITING
NA
Computerized Questionnaires in Assessing Symptoms, Pain, Depression, and Physical Function in Patients With Metastatic and/or Advanced Locoregional Cancer
NCT00972634
COMPLETED
Study of the Life Stories of Patients Making a Request for Euthanasia, in the Context of Advanced Cancer.
NCT05884788
COMPLETED
Cancer Fatigue Education Program
NCT01278147
COMPLETED
NA
Perceived Burden and Quality of Life of Primary Caregivers of Cancer Patients Aged 70 and Older After 5 Years of Management
NCT04478903
COMPLETED
Existential Distress in Patients with Advanced Cancer and Their Caregivers
NCT04600206
COMPLETED
Health-Related Quality of Life Coupled With Therapeutic Information on Compliance to Endocrine Therapy in Breast Cancer
NCT04176809
RECRUITING
NA
Safety and Feasibility of a Multidisciplinary Programme of Integrated Hospital-home Management With Early Discharge of Patients With Haematological Malignancies Undergoing High-dose Chemotherapy in Hospital
NCT06814405
RECRUITING
NA
Uncertainty in Illness in Palliative Care: an Intervention for Family Caregivers
NCT03518970
UNKNOWN
NA
Evaluation of Tolerance and Quality of Life in Patients With Neuroendocrine Tumors Treated With Oral Anti-Tumor Drugs Within a Therapeutic Education Program
NCT07258810
NOT_YET_RECRUITING
Prospective Study of the Perception of Palliative Care by Relatives of Patients Treated in Oncology
NCT01936428
COMPLETED
NA
Feasibility of Quality of Life Assessment in Routine Clinical Oncology Practice at the University Hospital of Besancon
NCT02844608
UNKNOWN
NA
Perceptions of Burden in Patients With Late-Stage Cancer and Their Caregivers
NCT00770419
WITHDRAWN
Existential Issues in Elderly People With Cancer
NCT01309815
COMPLETED
Analysis of COMPASsion and Humanisation of Adolescents Facing the End-of-life Processes.
NCT06310434
ENROLLING_BY_INVITATION
A Feasibility Study in Chronically Fatigued Cancer Survivors
NCT04931407
COMPLETED
NA
Assessment and Prevention of Caregiver Burden in Oncology
NCT05750836
NOT_YET_RECRUITING
NA
Identification of Palliative Care Needs and Prognostic Factors of Survival in Tailoring Appropriate Interventions in Advanced Oncological, Renal and Pulmonary Diseases
NCT06909968
COMPLETED
Incidence and Risk Factors of Prolonged Grief in Palliative Care Units
NCT03748225
COMPLETED