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Choice of Diction's Effect

Not Applicable
Conditions
Communication
Advance Directives
Decision Making
Cardiopulmonary Resuscitation
Interventions
Other: Alternative phrasing for no code
Other: Standard of care for no code
Registration Number
NCT04896411
Lead Sponsor
Rutgers, The State University of New Jersey
Brief Summary

The purpose of the research is to determine how the language used when discussing preferences about cardiopulmonary resuscitation (CPR) affects decisions regarding this (code status)

Detailed Description

Most Americans express a preference for dying at home naturally and surrounded by loved ones. However, many also believe that cardiopulmonary resuscitation (CPR) is more effective than it is, and want to have CPR even when the chances for a good outcome is poor. Among other reasons, the alternative term (Do Not Resuscitate, or DNR) has been shown in the literature to be associated by patients with passive, sub-optimal, and low quality care.

This study will attempt to determine patient preference for the "no CPR" term on patients admitted to the hospital using alternate phrasing. During admission to the Medical Teaching Service, patients over the age of 65 who are able to consent and who are not critically ill/unstable will be approached. After checking brief background questions (such as if they ever had discussions like these before), they will be randomized into two groups and asked code status using one of the two phrases. This question will determine the patient's "code status;" asking for this is a routine part of hospitalized care that is required by law (the exact terminology is left to the care team). After determining the patient's code status, they will be asked how satisfied they were with the decision; the investigator will be asked if they agree with the decision separately. Demographic and clinical information will be collected. Six months later, the patient will be contacted again; at this time, they will be asked about recent life and health changes. Finally, they will be asked their code status one more time. This will conclude the participant's involvement in the study

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • 65 or older
  • English-fluency in reading and speaking
  • Capacity to consent
Exclusion Criteria
  • Unstable psychiatric illness
  • Unstable/critically ill patients requiring ICU-level care
  • Active substance abuse

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Alternative PhraseAlternative phrasing for no codeThis arm will have the code status question randomized to offer CPR vs the alternative phrase
Standard of care phraseStandard of care for no codeThis arm will have the code status question randomized to offer CPR vs the standard of care phrase
Primary Outcome Measures
NameTimeMethod
Code Status SelectionImmediately collected after consent and randomization into a study arm

Selection of "code" versus "no code" decision depending on phrasing used, stratified by GO-FAR calculation

Secondary Outcome Measures
NameTimeMethod
Participant Satisfaction with DecisionImmediately collected after consent and randomization into a study arm

Determine patient satisfaction of, and provider agreement with, code discussion. The former will be measured using a modified Satisfaction with Decision Scale, a six-item Likert scale indicating agreement or not with the statements provided. The latter will be determined by asking the physician if they agree (yes/no/unsure)

Length of ConversationImmediately collected after consent and randomization into a study arm

Determine whether there is a difference of conversation length between phrasing groups (measured in minutes)

Trial Locations

Locations (1)

Robert Wood Johnson University Hospital, New Brunswick

🇺🇸

New Brunswick, New Jersey, United States

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