Trial Outcomes & Findings for Colorectal Cancer Screening in Alaska Native Men (NCT NCT06436300)

NCT ID: NCT06436300

Last Updated: 2025-08-29

Results Overview

Screening procedure documented in the electronic medical record

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

998 participants

Primary outcome timeframe

Six months

Results posted on

2025-08-29

Participant Flow

The trial obtained a waiver of consent, and no individuals were directly recruited or enrolled. Screening-eligible men who met all other criteria were identified in the electronic health record and randomly sampled for inclusion in the study cohort.

Prior to sending the first electronic message, we re-queried the electronic health record and removed men who had completed colorectal screening in the interval between randomization and launching the trial.

Participant milestones

Participant milestones
Measure
Control
The control arm received usual care for colorectal cancer screening outreach, and did not receive any study-related electronic messages.
Messages
This arm received electronic messages to promote colorectal cancer screening, but did not receive any notices about additional incentives.
Gift Card
This arm received the same electronic messages as the "Messages" arm, and was additionally promised a $50 gift card if they completed colorectal screening by the target date.
Raffle
This arm received the same electronic messages as the "Messages" arm, and were additionally promised they would be added to a raffle (\~$200 prize value) if they completed screening before a target date.
Overall Study
STARTED
250
250
248
250
Overall Study
COMPLETED
250
250
248
250
Overall Study
NOT COMPLETED
0
0
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Colorectal Cancer Screening in Alaska Native Men

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Control
n=250 Participants
The control arm received usual care for colorectal cancer screening outreach, and did not receive any study-related electronic messages.
Messages
n=250 Participants
This arm received electronic messages to promote colorectal cancer screening, but did not receive any notices about additional incentives.
Gift Card
n=248 Participants
This arm received the same electronic messages as the "Messages" arm, and was additionally promised a $50 gift card if they completed colorectal screening by the target date.
Raffle
n=250 Participants
This arm received the same electronic messages as the "Messages" arm, and were additionally promised they would be added to a raffle (\~$200 prize value) if they completed screening before a target date.
Total
n=998 Participants
Total of all reporting groups
Sex: Female, Male
Female
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
Sex: Female, Male
Male
250 Participants
n=39 Participants
250 Participants
n=41 Participants
248 Participants
n=35 Participants
250 Participants
n=31 Participants
998 Participants
n=146 Participants
Race (NIH/OMB)
American Indian or Alaska Native
250 Participants
n=39 Participants
250 Participants
n=41 Participants
248 Participants
n=35 Participants
250 Participants
n=31 Participants
998 Participants
n=146 Participants
Race (NIH/OMB)
Asian
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)
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
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)
White
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)
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
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
Previous screening
Previously screened
36 Participants
n=39 Participants
40 Participants
n=41 Participants
36 Participants
n=35 Participants
40 Participants
n=31 Participants
152 Participants
n=146 Participants
Previous screening
Not previously screened
214 Participants
n=39 Participants
210 Participants
n=41 Participants
212 Participants
n=35 Participants
210 Participants
n=31 Participants
846 Participants
n=146 Participants
Age, Customized
40-44 years
78 Participants
n=39 Participants
82 Participants
n=41 Participants
87 Participants
n=35 Participants
79 Participants
n=31 Participants
326 Participants
n=146 Participants
Age, Customized
45-49 years
47 Participants
n=39 Participants
47 Participants
n=41 Participants
40 Participants
n=35 Participants
47 Participants
n=31 Participants
181 Participants
n=146 Participants
Age, Customized
50-54 years
46 Participants
n=39 Participants
40 Participants
n=41 Participants
39 Participants
n=35 Participants
29 Participants
n=31 Participants
154 Participants
n=146 Participants
Age, Customized
55-59 years
29 Participants
n=39 Participants
29 Participants
n=41 Participants
26 Participants
n=35 Participants
32 Participants
n=31 Participants
116 Participants
n=146 Participants
Age, Customized
60-65 years
50 Participants
n=39 Participants
52 Participants
n=41 Participants
56 Participants
n=35 Participants
63 Participants
n=31 Participants
221 Participants
n=146 Participants

PRIMARY outcome

Timeframe: Six months

Screening procedure documented in the electronic medical record

Outcome measures

Outcome measures
Measure
Control
n=250 Participants
The control arm received usual care for colorectal cancer screening outreach, and did not receive any study-related electronic messages.
Messages
n=250 Participants
This arm received electronic messages to promote colorectal cancer screening, but did not receive any notices about additional incentives.
Gift Card
n=248 Participants
This arm received the same electronic messages as the "Messages" arm, and was additionally promised a $50 gift card if they completed colorectal screening by the target date.
Raffle
n=250 Participants
This arm received the same electronic messages as the "Messages" arm, and were additionally promised they would be added to a raffle (\~$200 prize value) if they completed screening before a target date.
Number of Participants Who Completed Colorectal Cancer Screening
Any screening documented
11 Participants
16 Participants
18 Participants
19 Participants
Number of Participants Who Completed Colorectal Cancer Screening
No screening documented
239 Participants
234 Participants
230 Participants
231 Participants

PRIMARY outcome

Timeframe: Six months

Pre-screening or screening visit scheduled in the electronic medical record during follow-up

Outcome measures

Outcome measures
Measure
Control
n=250 Participants
The control arm received usual care for colorectal cancer screening outreach, and did not receive any study-related electronic messages.
Messages
n=250 Participants
This arm received electronic messages to promote colorectal cancer screening, but did not receive any notices about additional incentives.
Gift Card
n=248 Participants
This arm received the same electronic messages as the "Messages" arm, and was additionally promised a $50 gift card if they completed colorectal screening by the target date.
Raffle
n=250 Participants
This arm received the same electronic messages as the "Messages" arm, and were additionally promised they would be added to a raffle (\~$200 prize value) if they completed screening before a target date.
Number of Participants Who Scheduled a Screening-related Visit
Visit scheduled
8 Participants
20 Participants
18 Participants
17 Participants
Number of Participants Who Scheduled a Screening-related Visit
No visit scheduled
242 Participants
230 Participants
230 Participants
233 Participants

Adverse Events

Control

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

Messages

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

Gift Card

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

Raffle

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

Clemma Muller

Washington State University

Phone: 612-327-7237

Results disclosure agreements

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