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The goal of this study is to evaluate whether an educational tool about colorectal cancer (CRC) completed on a computer that helps patients clarify their CRC screening preferences will lead to increased screening rates for CRC compared to standard information delivered via computer.
Background: Colorectal cancer (CRC) is a significant and preventable disease, yet CRC screening remains one of the lowest quality indicators in the VA healthcare system. Moreover, a recent VA directive recommends that CRC screening among Veterans should be based on their preferences, given that there is insufficient evidence to support recommending one test. However the impact of such a preference-based strategy on important outcomes, including screening adherence and cost, is unknown.
Objectives: The broad hypothesis of the proposed study is that helping Veterans clarify their CRC screening preferences will lead to increased adherence. The framework conceptualizes that preference clarification leads to more informed decision-making and, eventually, to better adherence with screening. The specific aims are: 1) To test the effectiveness of a preference-tailored (PT) vs. standard information (SI) intervention for increasing Veterans' CRC screening adherence; 2) To assess the impact of the intervention on informed decision making, knowledge and attitudes toward screening, decisional outcomes, and intention to get screened; and 3) To conduct a cost effectiveness analysis of the PT intervention for increasing CRC screening across the VA.
Methods: A randomized controlled trial of the PT vs. SI decision tool will be conducted in the Ann Arbor and Pittsburgh VA healthcare systems. The intervention was developed by the PI working with the Center for Health Communication Research at the University of Michigan. Eligible patients will be 552 (276 per group) Veterans between 50 and 78 who are due for CRC screening, and who have a primary care visit scheduled within the upcoming 4-6 weeks. Those at high risk (e.g., family or personal history of CRC) will be excluded. Providers will be informed of the study via regular mail and email. In Ann Arbor providers will be given the opportunity to opt-out their participants if they choose to do so. In Pittsburgh providers will be given lists of their participants as they are being considered for the study and will be given the chance to remove any potential participants from the contact list. Potential participants will be mailed an introductory letter. Those who do not opt-out will contacted by telephone. Participants will come to their primary care visit 40 minutes early, at which time they will complete informed consent. The intervention will be delivered via the Internet, and participants will be randomized to the PT or SI arm at the time of log-in. Study measures are consistent with the conceptual framework and based on the Preventive Health Model. Preference information will be collected through the computer program. Secondary outcomes and independent variables will be collected via telephone survey 3 days following the intervention. Adherence to screening will be collected from medical charts at 6 months. CRC screening information in a sub-sample of 80 Ann Arbor Veterans, not in either the PT or SI groups, will also be collected to measure "usual care" (UC). Pittsburgh will use the External Peer Review Program (EPRP) for the collection of clinical performance measures, more specifically CRC screening rates, to serve as an effective substitute for the UC group. Hypotheses related to each aim will be tested using multi-level modeling to control for between-provider effects. The overall hypothesis is that patients in the PT group will have higher rates of adherence to CRC screening at the 6 month follow-up point. Cost effectiveness analysis will determine whether a preference-based screening strategy could be cost effective for the VA healthcare system. The PI will work with the investigative team to disseminate the results through local and national VA websites, publications and presentations.
Status: Active, not recruiting.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Preference-tailored (PT) intervention | Experimental | Intervention: Behavioral: Standard Information Behavioral: Preference-tailored Information |
|
| Standard information (SI) intervention | Active Comparator | Behavioral: Standard Information |
|
| Usual Care | No Intervention | Due to budget and time constraints this group was not powered as a true study arm but was used to assess the impact of our baseline physician information letter and to control for any other interventions of system-wide initiatives that may occur during the study timeframe and impact rated of CRC screening. Data was not collected on every participant in this arm. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Standard Information | Behavioral | A computer based educational overview of CRC and CRC test options will be presented to the subject. The subject will be given a handout with a brief description of each of the screening options and will include the test that they have chosen as their preferred test. The subjects will be asked to take this handout to their upcoming clinic appointment and to discuss the screening options with their care provider. |
| Measure | Description | Time Frame |
|---|---|---|
| Colorectal Cancer (CRC) Screening Rate. | The CRC Screening rate reports percentage of participant adherence with any Colorectal Cancer Screening test within 6 months of Decider Guider intervention. Decider Guider is a tool to help patients make an informed choice about colon cancer testing. | Within 6 months of Decider Guider intervention. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Elements of Braddock's Informed Decision Making (IDM) Model Discussed With Provider | Outcome measure using 6 items measuring degree of participation in IDM. Scaled and recategorized into Low, Moderate and High level of IDM. The range is from 1 (low level of IDM) to 6 (high level of IDM). | 3-5 days after Decider Guider intervention |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sarah T Hawley, PhD MPH BA | Ann Arbor VA Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| VA Ann Arbor Healthcare System | Ann Arbor | Michigan | 48113-0170 | United States | ||
| Center for Health Equity Research and Promotion |
The Usual Care group is not counted toward the Enrollment total. See description of group below for additional details.
The Usual Care group is not counted toward the Enrollment total. See description of group below for additional details.
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| ID | Title | Description |
|---|---|---|
| FG000 | Preference-tailored (PT) Intervention | Standard Information: A computer based educational overview of CRC and CRC test options was presented to the subject. The subject was given a handout with a brief description of each of the screening options and which included the test that they have chosen as their preferred test. The subjects were asked to take this handout to their upcoming clinic appointment and to discuss the screening options with their care provider. Preference-tailored Information: A preference elicitation exercise generated a list of the three top attributes for the subject and the CRC screening test most consistent with these attributes. Subjects were provided with a handout to take to their clinic appointment as were the Standard Information group, but with the addition of a listing of their top attributes and the test most consistent with their top attributes. |
| FG001 | Standard Information (SI) Intervention | Standard Information: A computer based educational overview of CRC and CRC test options was presented to the subject. The subject was given a handout with a brief description of each of the screening options and which included the test that they have chosen as their preferred test. The subjects were asked to take this handout to their upcoming clinic appointment and to discuss the screening options with their care provider. |
| FG002 | Usual Care | Due to budget and time constraints this group is not powered as a true study arm but is being used to assess the impact of our baseline physician information letter and to control for any other interventions of system-wide initiatives that may have occurred during the study timeframe and impact rated of CRC screening. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
Baseline participants in Arm 1 and 2 reflect the number completing the survey. Not all participants enrolled to these arms completed the survey. Arm 3, "usual care" arm, was not a true 3rd arm and participants in this group did not complete the survey.
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| ID | Title | Description |
|---|---|---|
| BG000 | Preference-tailored (PT) Intervention | Preference-tailored Information: A preference elicitation exercise generated a list of the three top attributes for the subject and the CRC screening test most consistent with these attributes. Subjects were provided with a handout to take to their clinic appointment as were the Standard Information group, but with the addition of a listing of their top attributes and the test most consistent with their top attributes. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Colorectal Cancer (CRC) Screening Rate. | The CRC Screening rate reports percentage of participant adherence with any Colorectal Cancer Screening test within 6 months of Decider Guider intervention. Decider Guider is a tool to help patients make an informed choice about colon cancer testing. | Posted | Number | percentage of participants | Within 6 months of Decider Guider intervention. |
|
1 year
All Serious Adverse Events were determined by the IRB to be unrelated to study participation.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Preference-tailored (PT) Intervention | Preference-tailored (PT) intervention |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hospitalization for Deep Venous Thrombus (DVT) and Abdominal Aortic Aneurysm (AAA) | Vascular disorders | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
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Usual care arm was not true 3rd arm. We identified pts meeting eligibility criteria & randomized ~ 10th pt to be followed, measuring CRC screening 6 mos later. No intervention or survey. Only 79.6% of those enrolled completed survey.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Sarah Hawley, Ph.D. | VA Ann Arbor Healthcare System, Center for Clinical Management Research | 734-936-8816 | sarahawl@umich.edu |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D010342 | Patient Acceptance of Health Care |
| D057240 | Patient Preference |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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|
| Preference-tailored Information | Behavioral | A preference elicitation exercise that will generate a list of the three top attributes for the subject and the CRC screening test most consistent with these attributes. Subjects will be provided with a handout to take to their clinic appointment as the Standard Information group does, but with the addition of a listing of their top attributes and the test most consistent with their top attributes. |
|
| Colorectal Cancer Screening (CRCS) Knowledge and Attitudes. |
Outcome measure measuring knowledge of CRCS using 8-item knowledge measure (all true/false questions) developed for study, scaled and categorized into low/moderate/high knowledge, where low = low knowledge and high = high knowledge. |
| 3-5 days after Decider Guider intervention. |
| Decisional Satisfaction | Outcome measures measuring decisional satisfaction using 7-item scale categorized into low, moderate, high. Decisional satisfaction is a measure that was first developed by Margaret Holmes Rover and colleagues (Med Decis Making. 1996 Jan-Mar;16(1):58-64) to assess the perspective of a patient involved in a medical decision with the decision making process. The measure includes questions related to overall satisfaction, and satisfaction with the amount of information received, involvement in, degree of consistency with values, and time to make the decision. The measure includes 5 questions each on a 5 point scale where higher scores = higher satisfaction. When scaled into one overall measure of decision satisfaction, lower scores = lower satisfaction and higher scores = higher satisfaction. | 3-5 days after Decider Guider intervention. |
| Intent to Get Colorectal Cancer Screening. | Outcome measure measuring intent to get CRC screening using 5-item stage of readiness scale. Intent is measured by looking at the highest 2 items (I think I will get screened and I am committed to getting screened). | 3-5 days after Decider Guider intervention. |
| Self Efficacy. | Outcome measure measuring self-efficacy using 5-item measure, dichotomized into low vs. high self-efficacy (confidence) in getting screened. | 3-5 days after Decider Guider intervention. |
| If Colorectal Cancer Screening Screening (CRCS) Discussed With Provider. | Outcome measure measuring percentage of participants discussing CRCS with provider using single question (yes/no): "did you discuss Colorectal Cancer Screening with your provider?" | 3-5 days after Decider Guider intervention. |
| Pittsburgh |
| Pennsylvania |
| 15240 |
| United States |
| BG001 | Standard Information (SI) Intervention | Standard Information: A computer based educational overview of CRC and CRC test options was presented to the subject. The subject was given a handout with a brief description of each of the screening options and which included the test that they have chosen as their preferred test. The subjects were asked to take this handout to their upcoming clinic appointment and to discuss the screening options with their care provider. |
| BG002 | Usual Care | Due to budget and time constraints this group is not powered as a true study arm but is being used to assess the impact of our baseline physician information letter and to control for any other interventions of system-wide initiatives that may have occurred during the study timeframe and impact rated of CRC screening. |
| BG003 | Total | Total of all reporting groups |
| Participants |
|
| Age, Continuous | Mean | Full Range | Years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| OG001 | Standard Information (SI) Intervention | Standard information (SI) intervention Behavioral: Standard Information Standard Information: A computer based educational overview of CRC and CRC test options will be presented to the subject. The subject will be given a handout with a brief description of each of the screening options and will include the test that they have chosen as their preferred test. The subjects will be asked to take this handout to their upcoming clinic appointment and to discuss the screening options with their care provider. |
| OG002 | Usual Care | "Usual Care" - due to budget and time constraints this group is not powered as a true study arm but is being used to assess the impact of our baseline physician information letter and to control for any other interventions of system-wide initiatives that may have occurred during the study timeframe and impact rated of CRC screening. |
|
|
| Secondary | Number of Elements of Braddock's Informed Decision Making (IDM) Model Discussed With Provider | Outcome measure using 6 items measuring degree of participation in IDM. Scaled and recategorized into Low, Moderate and High level of IDM. The range is from 1 (low level of IDM) to 6 (high level of IDM). | Data was not collected for Usual Care arm. | Posted | Mean | Full Range | Degree of participation | 3-5 days after Decider Guider intervention |
|
|
|
|
| Secondary | Colorectal Cancer Screening (CRCS) Knowledge and Attitudes. | Outcome measure measuring knowledge of CRCS using 8-item knowledge measure (all true/false questions) developed for study, scaled and categorized into low/moderate/high knowledge, where low = low knowledge and high = high knowledge. | Data was not collected for Usual Care arm. | Posted | Number | percentage of participants | 3-5 days after Decider Guider intervention. |
|
|
|
|
| Secondary | Decisional Satisfaction | Outcome measures measuring decisional satisfaction using 7-item scale categorized into low, moderate, high. Decisional satisfaction is a measure that was first developed by Margaret Holmes Rover and colleagues (Med Decis Making. 1996 Jan-Mar;16(1):58-64) to assess the perspective of a patient involved in a medical decision with the decision making process. The measure includes questions related to overall satisfaction, and satisfaction with the amount of information received, involvement in, degree of consistency with values, and time to make the decision. The measure includes 5 questions each on a 5 point scale where higher scores = higher satisfaction. When scaled into one overall measure of decision satisfaction, lower scores = lower satisfaction and higher scores = higher satisfaction. | Data was not collected for Usual Care arm. | Posted | Number | Percentage of participants | 3-5 days after Decider Guider intervention. |
|
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|
|
| Secondary | Intent to Get Colorectal Cancer Screening. | Outcome measure measuring intent to get CRC screening using 5-item stage of readiness scale. Intent is measured by looking at the highest 2 items (I think I will get screened and I am committed to getting screened). | Data was not collected for Usual Care arm. | Posted | Number | percentage of participants | 3-5 days after Decider Guider intervention. |
|
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|
|
| Secondary | Self Efficacy. | Outcome measure measuring self-efficacy using 5-item measure, dichotomized into low vs. high self-efficacy (confidence) in getting screened. | Data was not collected for Usual Care arm. | Posted | Number | percentage of participants | 3-5 days after Decider Guider intervention. |
|
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|
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| Secondary | If Colorectal Cancer Screening Screening (CRCS) Discussed With Provider. | Outcome measure measuring percentage of participants discussing CRCS with provider using single question (yes/no): "did you discuss Colorectal Cancer Screening with your provider?" | Data was not collected for Usual Care arm. | Posted | Number | percentage of participants | 3-5 days after Decider Guider intervention. |
|
|
|
|
| 3 |
| 232 |
| 0 |
| 232 |
| EG001 | Standard Information (SI) Intervention | Standard information (SI) intervention | 3 | 234 | 0 | 234 |
| EG002 | Usual Care | "Usual Care" - due to budget and time constraints this group was not powered as a true study arm but was used to assess the impact of our baseline physician information letter and to control for any other interventions of system-wide initiatives that may occur during the study timeframe and impact rated of CRC screening. Data was not collected on every participant in this arm. | 0 | 84 | 0 | 84 |
|
| Hospitalization for Acute Renal Failure and Diastolic Heart Failure. | Renal and urinary disorders | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
|
| Emergency room visit for atrial flutter; death 53 days later noted in chart, cause unknown | Cardiac disorders | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
|
| Hospitalization for esophageal cancer. | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
|
| Hospitalization for depression and alcohol intoxication | Psychiatric disorders | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
|
| Death due to myocardial infarction. | Cardiac disorders | Non-systematic Assessment | The IRB determined this SAE to be unrelated to study participation. |
|
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| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |
| D000074822 | Treatment Adherence and Compliance |
| D015438 | Health Behavior |
| D001519 | Behavior |
| D017060 | Patient Satisfaction |
| High |
|
| High |
|