Trial Outcomes & Findings for PRISM Race and Communication Pilot RCT (NCT NCT04915079)

NCT ID: NCT04915079

Last Updated: 2026-04-30

Results Overview

We will measure the change the Connor-Davidson Resilience Scale (CD-RISC 10) between enrollment and at 3-months after randomization. in The 10-item Connor-Davidson Resilience Scale (CD-RISC) is is composed of 10 items from an original 25-item CD-RISC scale. Scores correlate with the full 25-item scale. Respondents rate their agreement with the survey items on a 5-point Likert scale from 0 (not true at all) to 4 (nearly true all the time). It is scored by the sum of all items with a range between 0-40 with higher scores indicating higher patient-reported resilience.

Recruitment status

COMPLETED

Study phase

PHASE1/PHASE2

Target enrollment

28 participants

Primary outcome timeframe

3 months

Results posted on

2026-04-30

Participant Flow

Patients eligible for screening will be Black patients hospitalized at Harborview Medical Center on an internal medicine or cardiology service. Potential participants will be screened in the electronic medical record. Eligible patients will be Black, diagnosed with a serious illness associated with a median expected survival of two years or less, English-speaking, age 18 years and older, and with no cognitive impairment.

Participant milestones

Participant milestones
Measure
PRISM
Patients in this arm will be recipients of the PRISM intervention
Usual Care
Patients in this arm will not receive the PRISM intervention, but will continue to receive usual care the discretion of their treating clinicians.
Overall Study
STARTED
13
15
Overall Study
Completed enrollment CD-RISC
13
15
Overall Study
COMPLETED
6
1
Overall Study
NOT COMPLETED
7
14

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

PRISM Race and Communication Pilot RCT

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
PRISM
n=6 Participants
Patients in this arm will be recipients of the PRISM intervention
Usual Care
n=1 Participants
Patients in this arm will not receive the PRISM intervention, but will continue to receive usual care the discretion of their treating clinicians.
Total
n=7 Participants
Total of all reporting groups
Age, Continuous
64.2 Years
STANDARD_DEVIATION 11.6 • n=14 Participants
50 Years
STANDARD_DEVIATION 0 • n=34 Participants
61.5 Years
STANDARD_DEVIATION 13.0 • n=69 Participants
Sex: Female, Male
Female
5 Participants
n=14 Participants
1 Participants
n=34 Participants
6 Participants
n=69 Participants
Sex: Female, Male
Male
1 Participants
n=14 Participants
0 Participants
n=34 Participants
1 Participants
n=69 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants
Race (NIH/OMB)
Asian
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants
Race (NIH/OMB)
Black or African American
6 Participants
n=14 Participants
1 Participants
n=34 Participants
7 Participants
n=69 Participants
Race (NIH/OMB)
White
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=14 Participants
0 Participants
n=34 Participants
0 Participants
n=69 Participants

PRIMARY outcome

Timeframe: 3 months

We will measure the change the Connor-Davidson Resilience Scale (CD-RISC 10) between enrollment and at 3-months after randomization. in The 10-item Connor-Davidson Resilience Scale (CD-RISC) is is composed of 10 items from an original 25-item CD-RISC scale. Scores correlate with the full 25-item scale. Respondents rate their agreement with the survey items on a 5-point Likert scale from 0 (not true at all) to 4 (nearly true all the time). It is scored by the sum of all items with a range between 0-40 with higher scores indicating higher patient-reported resilience.

Outcome measures

Outcome measures
Measure
PRISM
n=6 Participants
Patients in this arm will be recipients of the PRISM intervention
Usual Care
n=1 Participants
Patients in this arm will not receive the PRISM intervention, but will continue to receive usual care the discretion of their treating clinicians.
10-item Connor-Davidson Resilience Scale (CD-RISC)
0.67 average of number of units on a scale
Standard Deviation 4.8
0 average of number of units on a scale
Standard Deviation 0

Adverse Events

PRISM

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Usual Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Crystal Brown

University of Washington

Phone: 206-744-5018

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place