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Project to Improve Communication About Serious Illness - Pilot Study (PICSI-P)

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University of Washington

Status

Completed

Conditions

Malignant Neoplasm
Diabetes Complications
Peripheral Vascular Disease
Liver Failures, Chronic
Lung Disease Chronic
Frail Elderly
Dementia
Leukemia, Lymphocytic, Chronic, B-Cell
Renal Insufficiency, Chronic
Congestive Heart Failure

Treatments

Behavioral: Jumpstart Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03746392
STUDY00004821

Details and patient eligibility

About

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.

Enrollment

150 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 2 patient groups

Jumpstart Intervention
Experimental group
Treatment:
Behavioral: Jumpstart Intervention
Usual Inpatient Hospital Care
No Intervention group

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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