Trial Outcomes & Findings for Low-Literacy Physician-Patient Intervention Promoting Colorectal Cancer Screening (NCT NCT01103479)
NCT ID: NCT01103479
Last Updated: 2015-05-06
Results Overview
CRC screening completion via Fecal Occult Blood Test (FOBT), Fecal Immunochemical Test (FIT) or Colonoscopy
COMPLETED
PHASE2/PHASE3
569 participants
within 6 months of provider recommendation
2015-05-06
Participant Flow
Recruitment for this study took place between September 15, 2010 and January 30, 2013 across seven federally qualified health centers as well as one large academic health center.
Enrolled participants were excluded from the trial before assignment to groups if they did not reach randomization (e.g. they did not reach the point in the pre-test survey where randomization took place. Therefore they were not assigned to groups. In this study, 3 of the 569 enrolled participants did not reach randomization.
Participant milestones
| Measure |
Control
Participants will complete interviewer-administered pre- and post-test
|
Physician Intervention
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer screening guidelines, communication skills, and health literacy training
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
|
Physician and Patient Intervention
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational DVD on CRC and CRC screening
|
|---|---|---|---|
|
Overall Study
STARTED
|
168
|
210
|
188
|
|
Overall Study
COMPLETED
|
163
|
201
|
174
|
|
Overall Study
NOT COMPLETED
|
5
|
9
|
14
|
Reasons for withdrawal
| Measure |
Control
Participants will complete interviewer-administered pre- and post-test
|
Physician Intervention
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer screening guidelines, communication skills, and health literacy training
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
|
Physician and Patient Intervention
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational DVD on CRC and CRC screening
|
|---|---|---|---|
|
Overall Study
Up to date with CRC screening
|
1
|
9
|
12
|
|
Overall Study
Family history of CRC
|
1
|
0
|
2
|
|
Overall Study
Active cancer
|
1
|
0
|
0
|
|
Overall Study
Saw non-study physician
|
2
|
0
|
0
|
Baseline Characteristics
Low-Literacy Physician-Patient Intervention Promoting Colorectal Cancer Screening
Baseline characteristics by cohort
| Measure |
Control
n=163 Participants
Participants will complete interviewer-administered pre- and post-test
|
Physician Intervention
n=201 Participants
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer screening guidelines, communication skills, and health literacy training
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
|
Physician and Patient Intervention
n=174 Participants
Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this condition will also view an educational DVD on CRC and CRC screening
|
Total
n=538 Participants
Total of all reporting groups
|
|---|---|---|---|---|
|
Age, Continuous
|
57.46 years
STANDARD_DEVIATION 6.07 • n=5 Participants
|
58.71 years
STANDARD_DEVIATION 6.24 • n=7 Participants
|
57.03 years
STANDARD_DEVIATION 6.09 • n=5 Participants
|
57.79 years
STANDARD_DEVIATION 6.17 • n=4 Participants
|
|
Sex: Female, Male
Female
|
124 Participants
n=5 Participants
|
144 Participants
n=7 Participants
|
129 Participants
n=5 Participants
|
397 Participants
n=4 Participants
|
|
Sex: Female, Male
Male
|
39 Participants
n=5 Participants
|
57 Participants
n=7 Participants
|
45 Participants
n=5 Participants
|
141 Participants
n=4 Participants
|
|
Race/Ethnicity, Customized
Non-Hispanic Black
|
82 participants
n=5 Participants
|
111 participants
n=7 Participants
|
93 participants
n=5 Participants
|
286 participants
n=4 Participants
|
|
Race/Ethnicity, Customized
Hispanic
|
68 participants
n=5 Participants
|
88 participants
n=7 Participants
|
75 participants
n=5 Participants
|
231 participants
n=4 Participants
|
|
Race/Ethnicity, Customized
Other/Missing
|
13 participants
n=5 Participants
|
2 participants
n=7 Participants
|
6 participants
n=5 Participants
|
21 participants
n=4 Participants
|
|
Region of Enrollment
United States
|
163 participants
n=5 Participants
|
201 participants
n=7 Participants
|
174 participants
n=5 Participants
|
538 participants
n=4 Participants
|
|
Survey Language
English
|
100 participants
n=5 Participants
|
118 participants
n=7 Participants
|
106 participants
n=5 Participants
|
324 participants
n=4 Participants
|
|
Survey Language
Spanish
|
63 participants
n=5 Participants
|
83 participants
n=7 Participants
|
68 participants
n=5 Participants
|
214 participants
n=4 Participants
|
|
Insurance Status (more than one may apply)
Private
|
21 participants
n=5 Participants
|
30 participants
n=7 Participants
|
27 participants
n=5 Participants
|
78 participants
n=4 Participants
|
|
Insurance Status (more than one may apply)
Medicare
|
47 participants
n=5 Participants
|
68 participants
n=7 Participants
|
52 participants
n=5 Participants
|
167 participants
n=4 Participants
|
|
Insurance Status (more than one may apply)
Medicaid
|
51 participants
n=5 Participants
|
71 participants
n=7 Participants
|
67 participants
n=5 Participants
|
189 participants
n=4 Participants
|
|
Insurance Status (more than one may apply)
Uninsured
|
66 participants
n=5 Participants
|
52 participants
n=7 Participants
|
42 participants
n=5 Participants
|
160 participants
n=4 Participants
|
|
Health Care System
Community FQHC
|
99 participants
n=5 Participants
|
174 participants
n=7 Participants
|
154 participants
n=5 Participants
|
427 participants
n=4 Participants
|
|
Health Care System
Academic Health Center
|
64 participants
n=5 Participants
|
27 participants
n=7 Participants
|
20 participants
n=5 Participants
|
111 participants
n=4 Participants
|
|
Years of Education
0 - 6 years
|
44 participants
n=5 Participants
|
38 participants
n=7 Participants
|
35 participants
n=5 Participants
|
117 participants
n=4 Participants
|
|
Years of Education
7 - 12 years
|
41 participants
n=5 Participants
|
64 participants
n=7 Participants
|
52 participants
n=5 Participants
|
157 participants
n=4 Participants
|
|
Years of Education
13 or more years
|
76 participants
n=5 Participants
|
98 participants
n=7 Participants
|
86 participants
n=5 Participants
|
260 participants
n=4 Participants
|
|
Years of Education
Missing data
|
2 participants
n=5 Participants
|
1 participants
n=7 Participants
|
1 participants
n=5 Participants
|
4 participants
n=4 Participants
|
|
Household Income
<$20,000/year
|
101 participants
n=5 Participants
|
137 participants
n=7 Participants
|
111 participants
n=5 Participants
|
349 participants
n=4 Participants
|
|
Household Income
$20,000 - $40,000/year
|
22 participants
n=5 Participants
|
28 participants
n=7 Participants
|
23 participants
n=5 Participants
|
73 participants
n=4 Participants
|
|
Household Income
$40,001 - $100,000/year
|
13 participants
n=5 Participants
|
6 participants
n=7 Participants
|
8 participants
n=5 Participants
|
27 participants
n=4 Participants
|
|
Household Income
Not sure/Don't know
|
23 participants
n=5 Participants
|
26 participants
n=7 Participants
|
27 participants
n=5 Participants
|
76 participants
n=4 Participants
|
|
Household Income
Refused/Missing
|
4 participants
n=5 Participants
|
4 participants
n=7 Participants
|
5 participants
n=5 Participants
|
13 participants
n=4 Participants
|
|
Health status
Poor
|
28 participants
n=5 Participants
|
28 participants
n=7 Participants
|
25 participants
n=5 Participants
|
81 participants
n=4 Participants
|
|
Health status
Fair
|
75 participants
n=5 Participants
|
107 participants
n=7 Participants
|
88 participants
n=5 Participants
|
270 participants
n=4 Participants
|
|
Health status
Good
|
39 participants
n=5 Participants
|
46 participants
n=7 Participants
|
44 participants
n=5 Participants
|
129 participants
n=4 Participants
|
|
Health status
Very Good
|
18 participants
n=5 Participants
|
10 participants
n=7 Participants
|
12 participants
n=5 Participants
|
40 participants
n=4 Participants
|
|
Health status
Excellent
|
2 participants
n=5 Participants
|
10 participants
n=7 Participants
|
4 participants
n=5 Participants
|
16 participants
n=4 Participants
|
|
Health status
Missing
|
1 participants
n=5 Participants
|
0 participants
n=7 Participants
|
1 participants
n=5 Participants
|
2 participants
n=4 Participants
|
|
Health Literacy
Inadequate
|
51 participants
n=5 Participants
|
86 participants
n=7 Participants
|
67 participants
n=5 Participants
|
204 participants
n=4 Participants
|
|
Health Literacy
Marginal/Adequate
|
96 participants
n=5 Participants
|
97 participants
n=7 Participants
|
88 participants
n=5 Participants
|
281 participants
n=4 Participants
|
|
Health Literacy
Missing
|
16 participants
n=5 Participants
|
18 participants
n=7 Participants
|
19 participants
n=5 Participants
|
53 participants
n=4 Participants
|
PRIMARY outcome
Timeframe: within 6 months of provider recommendationCRC screening completion via Fecal Occult Blood Test (FOBT), Fecal Immunochemical Test (FIT) or Colonoscopy
Outcome measures
| Measure |
Control
n=163 Participants
Participants will complete interviewer-administered pre- and post-test
|
Intervention
n=375 Participants
Participants in either the Physician Intervention or Physician and Patient Intervention Arms.
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
Physician and Patient Intervention: Physician intervention as described plus patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this co
|
|---|---|---|
|
Colorectal Cancer (CRC) Screening Completion
|
17 participants
|
69 participants
|
PRIMARY outcome
Timeframe: within 6 months of provider recommendationCRC screening completion via FOBT, FIT or Colonoscopy
Outcome measures
| Measure |
Control
n=201 Participants
Participants will complete interviewer-administered pre- and post-test
|
Intervention
n=174 Participants
Participants in either the Physician Intervention or Physician and Patient Intervention Arms.
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
Physician and Patient Intervention: Physician intervention as described plus patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this co
|
|---|---|---|
|
Colorectal Cancer (CRC) Screening Completion
|
41 participants
|
28 participants
|
SECONDARY outcome
Timeframe: 6 months following patient enrollment into studyProvider recommendation of CRC Screening based on chart review
Outcome measures
| Measure |
Control
n=163 Participants
Participants will complete interviewer-administered pre- and post-test
|
Intervention
n=375 Participants
Participants in either the Physician Intervention or Physician and Patient Intervention Arms.
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
Physician and Patient Intervention: Physician intervention as described plus patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this co
|
|---|---|---|
|
Provider Recommendation of CRC Screening
|
70 participants
|
216 participants
|
SECONDARY outcome
Timeframe: 6 months following patient enrollment into studyProvider recommendation of CRC Screening based on chart review
Outcome measures
| Measure |
Control
n=201 Participants
Participants will complete interviewer-administered pre- and post-test
|
Intervention
n=174 Participants
Participants in either the Physician Intervention or Physician and Patient Intervention Arms.
Physician Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training
Physician and Patient Intervention: Physician intervention as described plus patients in this condition will also view an educational digital video disc (DVD) on CRC and CRC screening
Physician and Patient Intervention: Physicians at these clinics will participate in 6 training sessions over the course of 3 1/2 years; training sessions relate to colorectal cancer (CRC) screening guidelines, communication skills, and health literacy training; patients in this co
|
|---|---|---|
|
Provider Recommendation of CRC Screening
|
113 participants
|
103 participants
|
Adverse Events
Control
Physician Training
Physician and Patient Intervention
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place