Exploring Indications and Practices of Administering Artificial Hydration to Terminal Cancer Patients in Taiwan

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorNational Taiwan University Hospital

About this trial

Background: The issue of artificial hydration for terminal cancer patients is a classic ethical dilemma in palliative care. It is a common practice especially when patients are incapable of oral intake; however, there is a lack of research on indications and practices for the provision of artificial hydration to terminal cancer patients in Taiwan. The investigators aim to conduct a nationwide survey of palliative care physicians on their indications (general or specific), and practices of providing artificial hydration to terminal cancer patients. With that understanding of reasoning and clinical practice, the investigators would further establish an indigenous, evidence-based consensus guideline to serve as a reference for physicians in Taiwan.

Methods: The study is comprised of two parts. The first part is to conduct a nationwide survey of palliative and oncology care specialists with a questionnaire designed from literature reviews and principles of clinical ethics. After validation of the questionnaire, the investigators will e-mail it to members of the Taiwan Academy of Hospice Palliative Medicine and the Taiwan Society of Cancer Palliative Medicine. The primary outcome measure of the study is the indication and clinical practice of artificial hydration, and the secondary outcome is factors associated with the administration or withdrawal of hydration.

The second part is to establish a national consensus on clinical guidelines for administering artificial hydration, where the investigators will conduct a modified Delphi method for 6 rounds. Literature reviews will be first performed and 14 sessions of one-to-one interviews in Round 1 to develop a draft. Subsequent rounds comprise questionnaire surveys among all panelists, teleconferences and e-mail discussions among core members, and cancer patients/patients' family discussions. Statistical criteria include median and disagreement scores according to the Inter-Percentile Range Adjusted for Symmetry. Items voted for by 70% or more panelists will be selected and formalized into a consensus guideline.

Expected results: The investigators hypothesize that the indication to administer artificial hydration to the terminal cancer patient is multi-factorial and culturally based.

Conclusion: The establishment of a consensus guideline will help clinicians to make an appropriate decision from ethical, medical, cultural, and emotional factors and facilitate cancer patients to achieve a good quality of dying.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Taiwan Academy of Hospice Palliative Medicine

Taiwan Society of Cancer Palliative Medicine

At least a year in training to take care of terminally ill patients

Have signed informed consent.

Disqualifiers

No clinical experience in palliative care

Decline to sign informed consent

Trial population

From the name list of the Taiwan Academy of Hospice Palliative Medicine and Taiwan Society of Cancer Palliative Medicine

Trial design

Design model

Other

Time perspective

Retrospective

Treatments tested in this trial

  • Administering of artificial hydration

    Behavioral

    Administering of artificial hydration to terminal cancer patients

Treatment groups

1,270 Participants
are divided into 2 treatment groups
Group A: members of the Taiwan Academy of Hospice Palliative Medicine1 intervention
Group B: members of the Taiwan Society of Cancer Palliative Medicine1 intervention

Trial outcomes

Primary outcomes

1

Likert scale on alteration of administer artificial hydration to the terminal cancer patient and principles of clinical ethics

Multi-factorial and culturally based questionnaire in a nationwide survey of palliative and oncology care specialist, to explore the 5- to 9-point scale of opinion on indication and practices of administrating artificial hydration to terminal cancer patients

Time frame
Within 1 month
2

Distributive statistics

Statistical analyses of quality indicators from 14 sessions of one-to-one interviews and questionnaire surveys among panelists, to be formalized into a consensus guideline when over 70% of panelists voting for a questionnaire item

Time frame
At most 6 months
3

Disagreement score according to the Interpercentile Range Adjusted for Symmetry (IPRAS) for survey results

Higher scores indicating a worse outcome

Time frame
Within 6 months

Secondary outcomes

Other outcomes

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