Trial Outcomes & Findings for CAMS-RAS: for Suicide Prevention (NCT NCT03072875)

NCT ID: NCT03072875

Last Updated: 2018-07-31

Results Overview

A brief face-valid, self-report measure that the PI derived from the System Usability Scale and has been successfully used in previous studies. Items are rated on a 5-point Likert Scale (1=poor; 3=good; 5=excellent). Includes open-ended questions to better understand what was most and least helpful with respect to each category and also measures users' acceptance.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

26 participants

Primary outcome timeframe

up to one day

Results posted on

2018-07-31

Participant Flow

Participant milestones

Participant milestones
Measure
CAMS-RAS
In this single-arm study design, all enrolled patient and non-patient participants are asked to provide feedback on the CAMS-RAS prototype as it is developed for this study. Feedback will be gathered via survey measure and interview. CAMS-RAS
Overall Study
STARTED
26
Overall Study
COMPLETED
25
Overall Study
NOT COMPLETED
1

Reasons for withdrawal

Reasons for withdrawal
Measure
CAMS-RAS
In this single-arm study design, all enrolled patient and non-patient participants are asked to provide feedback on the CAMS-RAS prototype as it is developed for this study. Feedback will be gathered via survey measure and interview. CAMS-RAS
Overall Study
Lost to Follow-up
1

Baseline Characteristics

Age collected from 24 patient participants only (2 unknown)

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
CAMS-RAS
n=26 Participants
In this single-arm study design, all enrolled patient and non-patient participants are asked to provide feedback on the CAMS-RAS prototype as it is developed for this study. Feedback will be gathered via survey measure and interview. CAMS-RAS
Age, Continuous
39.38 Years
STANDARD_DEVIATION 12.76 • n=24 Participants • Age collected from 24 patient participants only (2 unknown)
Sex/Gender, Customized
Male
6 Participants
n=26 Participants
Sex/Gender, Customized
Female
16 Participants
n=26 Participants
Sex/Gender, Customized
Other
1 Participants
n=26 Participants
Sex/Gender, Customized
Unknown
3 Participants
n=26 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
n=26 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
21 Participants
n=26 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
3 Participants
n=26 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=26 Participants
Race (NIH/OMB)
Asian
1 Participants
n=26 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=26 Participants
Race (NIH/OMB)
Black or African American
1 Participants
n=26 Participants
Race (NIH/OMB)
White
18 Participants
n=26 Participants
Race (NIH/OMB)
More than one race
3 Participants
n=26 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants
n=26 Participants

PRIMARY outcome

Timeframe: up to one day

Population: Suicidal ED Patients only

A brief face-valid, self-report measure that the PI derived from the System Usability Scale and has been successfully used in previous studies. Items are rated on a 5-point Likert Scale (1=poor; 3=good; 5=excellent). Includes open-ended questions to better understand what was most and least helpful with respect to each category and also measures users' acceptance.

Outcome measures

Outcome measures
Measure
CAMS-RAS
n=6 Participants
In this single-arm study design, all enrolled patient and non-patient participants are asked to provide feedback on the CAMS-RAS prototype as it is developed for this study. Feedback will be gathered via survey measure and interview. CAMS-RAS
Usability Satisfaction and Acceptability Questionnaire (USAQ)
4.5 units on a scale
Standard Deviation 0.41

PRIMARY outcome

Timeframe: After interacting with the technology (length: approximately 1 hour), subjects were then asked to complete the semi-structured interview conducted by the research assistant. On average, the interview lasted approximately 15 minutes.

Population: The qualitative information from the semi-structured interviews tells us subjects' general opinions and preferences concerning the avatar.

A semi-structured interview was conducted following use of the CAMS-RAS tool to assess users' likes, dislikes, and other preferences. Questions included: "What were your experiences in using 'Dr. Dave' and the CAMS-RAS system?" and "What suggestions would you have for improvement?" All subjects indicated that they found the tool helpful to them. They described the tool using adjectives similar to those used to describe "Nurse Louise" - a "discharge nurse" avatar on which the investigator's avatar was based: "He's kind and asks me really practical, helpful questions"; "He speaks to me directly in a compassionate way"; and "He is kind and invested".

Outcome measures

Outcome measures
Measure
CAMS-RAS
n=6 Participants
In this single-arm study design, all enrolled patient and non-patient participants are asked to provide feedback on the CAMS-RAS prototype as it is developed for this study. Feedback will be gathered via survey measure and interview. CAMS-RAS
Number of ED Patient Participants Who Completed Semi-Structured Interview
6 Participants

Adverse Events

CAMS-RAS

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

Linda Dimeff, PhD

Evidence-Based Practice Institute

Phone: 206-455-7934

Results disclosure agreements

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