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N/A N=150 Randomized Single-blind Supportive Care

Project to Improve Communication About Serious Illness - Pilot Study

Malignant Neoplasm · Leukemia, Lymphocytic, Chronic, B-Cell · Lung Disease Chronic · Congestive Heart Failure · Liver Failures, Chronic

Enrolled (actual)
150
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcome: Primary: Documentation of Goals of Care — 16; 6 Participants — p=0.036

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Jumpstart Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Washington
Primary completion
Jun 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Documentation of Goals of Care
16; 6 0.036 sig

Summary

This two-year pilot study will test whether a one-page "Jumpstart Form" will affect goals-of-care discussions in the hospital. This form will be provided to clinicians and will include patient-specific information about preferences for goals-of-care communication and for care, as well as tips to improve this communication. Jumpstart forms will also be provided to patients or, if they are unable to communicate, their surrogates/family members. The information on the form will be obtained from questionnaires. The form is tailored to help patients and surrogates talk with clinicians about goals of care. This study is based on a successful application of Jumpstart Form in the outpatient clinic setting.

Eligibility Criteria

Inclusion Criteria, Patients: meeting criteria for serious illness (encompassing multiple acute and chronic illnesses) including:

  • those used by the Dartmouth Atlas to study end-of-life care in the US: malignant cancer/leukemia, chronic pulmonary disease, coronary artery disease, congestive heart failure, chronic liver disease, chronic renal disease, dementia, diabetes with end-organ damage, and peripheral vascular disease.
  • patients over age 65 with markers of frailty: albumin level <3.0 within 48 hours of admission and weight loss of ≥10 pounds in the past year.
  • hospitalized patients over age 80.
  • English-speaking

Exclusion Criteria, Patients:

  • unable to complete informed consent procedures and do not have a legal next of kin
  • restricted information status (e.g. prisoners)
  • pregnant

Inclusion Criteria, Surrogates:

  • involved in the care of an eligible patient as the legal next-of-kin
  • English-speaking

Exclusion Criteria, Surrogates:

  • unable to complete informed consent procedures
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03746392). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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