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A Culturally Sensitive Values-Guided Aid for End of Life Decision-Making

A Culturally Sensitive Values-Guided Aid for End of Life Decision-Making

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00122135
Acronym
Aim3
Enrollment
120
Registered
2005-07-21
Start date
2004-12-31
Completion date
2009-09-30
Last updated
2015-12-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease, Chronic Obstructive Pulmonary Disease, Cirrhosis, Colon Carcinoma, Congestive Heart Failure, Lung Cancer

Keywords

end-of-life care, clinical decision-making, values inventory, racial disparities

Brief summary

The goal of this research agenda is to improve the quality of end-of-life care by explicitly identifying values that will guide the decision-making process, with a particular emphasis on the role of ethnic, racial and cultural factors.

Detailed description

Background: End-of-life decision-making is an important aspect of providing quality healthcare, especially for the elderly population. Increasingly, the appropriateness of many of these decisions is being questioned. Some invasive procedures done in seriously ill patients do not significantly alter their course, many patients die without having pain or other symptoms addressed, and families may feel dissatisfied with the care provided. Additionally, there are striking racial/ethnic disparities in end-of-life care. Objectives: The explicit identification of values that guide medical decision-making could improve the decision-making process for end-of-life care for patients of all races/ethnicities. 1) We will directly compare, critically assess, and revise two Values Histories on the basis of qualitative data derived from individual interviews with racially/ethnically diverse patients and surrogates, and explore patients', surrogates', and physicians' values, preferences and concerns that guide decision-making about medical interventions at the end-of-life. 2) We will then adapt the existing Values Histories into a clinically practical tool, the Values Inventory discussion aid. 3) We will conduct preliminary testing of this tool to be used in physician-patient or physician-surrogate encounters to improve and facilitate decisions about end-of-life care. Methods: To complete Objective 3 we will conduct a pilot randomized trial of the developed Values Inventory discussion aid to test the feasibility of using it in clinical practice. This clinicaltrials.gov number applies to Objective 3 of IIR-02-224 only (as the complete study is a mixed-methods study with several different arms and enrollment goals). Eligible patients are at risk for 6-12-month mortality with one of the following diagnoses: congestive heart failure, with ejection fraction of less than 25%; severe chronic obstructive pulmonary disease/emphysema with dependence on oxygen; chronic liver disease with cirrhosis and ascites; colon carcinoma with liver metastases; or non-small cell cancer of the lung, stage III or IV, and patients with chronic kidney disease on renal replacement therapy, with previous hospitalization. All (patient) participants are age 55 years or older and are recruited through the clinics/wards at the Houston VAMC. Surrogates are surrogates of patients with such conditions; physicians are generalists and medical subspecialists. All participants are African American, Hispanic, or White, reflecting the 3 major races/ethnicities at the Houston VAMC.

Interventions

OTHERValues Inventory (VI)

The Values Inventory was given to patients for self-administration while they were awaiting their clinic appointment. They were instructed to bring it to their physician's attention right at the beginning of their clinic visit.

Sponsors

Baylor College of Medicine
CollaboratorOTHER
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Eligible patients will be at risk for 6-12 month mortality and have one of the following diagnoses: * congestive heart failure, with ejection fraction of \<25%; * severe chronic obstructive pulmonary disease/emphysema with dependence on oxygen; * chronic liver disease with cirrhosis and ascites; * colon carcinoma with liver metastases; or * non-small cell cancer of the lung, stage III or IV * chronic kidney disease on renal replacement therapy, with previous hospitalization * All participants will be age 55 years or older and will be recruited through the clinics at the Houston VAMC.

Exclusion criteria

* Patients with dementia * Patients less than 55 years old

Design outcomes

Primary

MeasureTime frameDescription
Presence of Discussions About End of Life Care Goals/WishesimmediateQualitative content analysis of physician-patient encounters regarding presence of any type of discussion about end of life care goals/wishes

Countries

United States

Participant flow

Participants by arm

ArmCount
Patients With VI
Patients who filled out the Values History prior to their clinic appointment
60
Patients Without VI
Patients who did not receive the Values History prior to their clinic appointment (usual care)
60
Total120

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject30

Baseline characteristics

CharacteristicPatients Without VIPatients With VITotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
33 Participants30 Participants63 Participants
Age, Categorical
Between 18 and 65 years
27 Participants30 Participants57 Participants
Age, Continuous68.4 years66.4 years67.4 years
Region of Enrollment
United States
60 participants60 participants120 participants
Sex: Female, Male
Female
0 Participants0 Participants0 Participants
Sex: Female, Male
Male
60 Participants60 Participants120 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 600 / 60
serious
Total, serious adverse events
0 / 600 / 60

Outcome results

Primary

Presence of Discussions About End of Life Care Goals/Wishes

Qualitative content analysis of physician-patient encounters regarding presence of any type of discussion about end of life care goals/wishes

Time frame: immediate

ArmMeasureValue (NUMBER)
Patients With VIPresence of Discussions About End of Life Care Goals/Wishes13 participants
Patients Without VIPresence of Discussions About End of Life Care Goals/Wishes8 participants
p-value: 0.77t-test, 2 sided

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026