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

Recruitment status

COMPLETED

Study phase

PHASE2/PHASE3

Target enrollment

569 participants

Primary outcome timeframe

within 6 months of provider recommendation

Results posted on

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

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

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

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 recommendation

CRC screening completion via Fecal Occult Blood Test (FOBT), Fecal Immunochemical Test (FIT) or Colonoscopy

Outcome measures

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 recommendation

CRC screening completion via FOBT, FIT or Colonoscopy

Outcome measures

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 study

Provider recommendation of CRC Screening based on chart review

Outcome measures

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 study

Provider recommendation of CRC Screening based on chart review

Outcome measures

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

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

Physician Training

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

Physician and Patient Intervention

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

Kenzie A. Cameron

Northwestern University

Phone: 312-503-3910

Results disclosure agreements

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