Trial Outcomes & Findings for Feasibility of a Colorectal Cancer Screening Web App in Primary Care Patients (NCT NCT06241768)
NCT ID: NCT06241768
Last Updated: 2025-06-05
Results Overview
Number (and proportion) of participants who are confirmed eligible for CRC screening and request a CRC screening test within the mPATH-CRC Web App
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
921 participants
Primary outcome timeframe
28 days
Results posted on
2025-06-05
Participant Flow
Participant milestones
| Measure |
Text Message 1
Version 1 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 2
Version 2 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 3
Version 3 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 4
Version 4 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
|---|---|---|---|---|
|
Overall Study
STARTED
|
232
|
230
|
229
|
230
|
|
Overall Study
Confirmed Eligible for CRC Screening
|
29
|
35
|
34
|
37
|
|
Overall Study
COMPLETED
|
232
|
230
|
229
|
230
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Feasibility of a Colorectal Cancer Screening Web App in Primary Care Patients
Baseline characteristics by cohort
| Measure |
Text Message 1
n=232 Participants
Version 1 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 2
n=230 Participants
Version 2 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 3
n=229 Participants
Version 3 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 4
n=230 Participants
Version 4 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Total
n=921 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
191 Participants
n=39 Participants
|
180 Participants
n=41 Participants
|
177 Participants
n=35 Participants
|
182 Participants
n=31 Participants
|
730 Participants
n=146 Participants
|
|
Age, Categorical
>=65 years
|
41 Participants
n=39 Participants
|
50 Participants
n=41 Participants
|
52 Participants
n=35 Participants
|
48 Participants
n=31 Participants
|
191 Participants
n=146 Participants
|
|
Sex: Female, Male
Female
|
134 Participants
n=39 Participants
|
142 Participants
n=41 Participants
|
137 Participants
n=35 Participants
|
138 Participants
n=31 Participants
|
551 Participants
n=146 Participants
|
|
Sex: Female, Male
Male
|
98 Participants
n=39 Participants
|
88 Participants
n=41 Participants
|
92 Participants
n=35 Participants
|
92 Participants
n=31 Participants
|
370 Participants
n=146 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
9 Participants
n=39 Participants
|
8 Participants
n=41 Participants
|
11 Participants
n=35 Participants
|
10 Participants
n=31 Participants
|
38 Participants
n=146 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
223 Participants
n=39 Participants
|
222 Participants
n=41 Participants
|
218 Participants
n=35 Participants
|
220 Participants
n=31 Participants
|
883 Participants
n=146 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
1 Participants
n=39 Participants
|
1 Participants
n=41 Participants
|
3 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
5 Participants
n=146 Participants
|
|
Race (NIH/OMB)
Asian
|
6 Participants
n=39 Participants
|
4 Participants
n=41 Participants
|
5 Participants
n=35 Participants
|
4 Participants
n=31 Participants
|
19 Participants
n=146 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
|
Race (NIH/OMB)
Black or African American
|
100 Participants
n=39 Participants
|
95 Participants
n=41 Participants
|
97 Participants
n=35 Participants
|
96 Participants
n=31 Participants
|
388 Participants
n=146 Participants
|
|
Race (NIH/OMB)
White
|
117 Participants
n=39 Participants
|
113 Participants
n=41 Participants
|
112 Participants
n=35 Participants
|
113 Participants
n=31 Participants
|
455 Participants
n=146 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
8 Participants
n=39 Participants
|
17 Participants
n=41 Participants
|
12 Participants
n=35 Participants
|
17 Participants
n=31 Participants
|
54 Participants
n=146 Participants
|
|
Region of Enrollment
United States
|
232 participants
n=39 Participants
|
230 participants
n=41 Participants
|
229 participants
n=35 Participants
|
230 participants
n=31 Participants
|
921 participants
n=146 Participants
|
PRIMARY outcome
Timeframe: 28 daysPopulation: Patients who used the mPATH-CRC Web App and were confirmed eligible for average-risk colorectal cancer screening
Number (and proportion) of participants who are confirmed eligible for CRC screening and request a CRC screening test within the mPATH-CRC Web App
Outcome measures
| Measure |
Text Message 1
n=29 Participants
Version 1 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 2
n=35 Participants
Version 2 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 3
n=34 Participants
Version 3 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 4
n=37 Participants
Version 4 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
|---|---|---|---|---|
|
Number (and Proportion) of Participants Who Request a Colorectal Cancer (CRC) Screening Test
|
16 Participants
|
17 Participants
|
22 Participants
|
19 Participants
|
SECONDARY outcome
Timeframe: 28 daysNumber (and proportion) of participants who complete the CRC screening eligibility questions within 4 weeks of the initial invitation using the mPATH-CRC Web App
Outcome measures
| Measure |
Text Message 1
n=232 Participants
Version 1 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 2
n=230 Participants
Version 2 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 3
n=229 Participants
Version 3 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
Text Message 4
n=230 Participants
Version 4 of the text message invitation to use the cloud-based colorectal cancer screening program
mPATH-CRC Web app: Cloud-based web application that informs individuals of colorectal cancer screening and helps them receive screening
|
|---|---|---|---|---|
|
Number (and Proportion) of Participants Who Complete the mPATH-CRC Web App
|
55 Participants
|
66 Participants
|
51 Participants
|
59 Participants
|
Adverse Events
Text Message 1
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Text Message 2
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Text Message 3
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Text Message 4
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
Dr. Anna Snavely
Wake Forest University School of Medicine
Phone: 336-716-2011
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place