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Shared Decision-Making for Colorectal Cancer Screening

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Web-based decision aid plus personalized risk assessment
Web-based decision aid alone
Generic website
Sponsored by
Agency for Healthcare Research and Quality (AHRQ)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring Colorectal cancer screening, Shared decision-making, Decision aid

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Asymptomatic average-risk subjects Under the direct care of one of participating site's staff (attending) physicians or physician extenders; No prior screening other than fecal occult blood testing (FOBT); No major co-morbidities that preclude CRC screening by any method Exclusion Criteria: Prior CRC screening by any method other than FOBT occult blood testing High-risk condition (personal history of colorectal cancer or polyps, family history of colorectal cancer or polyps involving one or more first degree relatives, chronic inflammatory bowel disease) Lack of fluency in written and spoken English (since decision aid and personalized risk assessment tool will be in English only due to funding issues); Comorbidities that preclude CRC screening by any method

Sites / Locations

  • Boston Medical Center
  • South Boston Community Health Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Sham Comparator

Arm Label

Decision aid plus YourDiseaseRisk

Decision aid alone

III

Arm Description

Patients viewed the decision aid and completed the Your Disease Risk risk assessment tool prior to visit with their primary care provider.

Patient's viewed decision aid only prior to a visit with their primary care provider.

Standard care

Outcomes

Primary Outcome Measures

Patient Adherence (Test Completion)
Completion of a screening test within 12 months of the study visit.

Secondary Outcome Measures

Patient Knowledge
Knowledge was assessed at baseline (pretest) and at the time of the exit survey (posttest) based on responses to a 12-item questionnaire (True/False/Don't know) that inquired about CRC risk factors, the rationale and goals of screening, and age at which screening should begin. Cumulative knowledge scores (range, 0-12) were derived by summing correct responses to the 12 individual knowledge questions.
Patient Satisfaction With Decision Making Process
Patient satisfaction with the decision-making process (SDMP) was assessed using the validated 12-item Satisfaction with the Decision-Making Process scale. Five ordered response categories were used for each item. Each response was assigned a point score ranging from 1 for "strongly disagree" (or "poor") to 5 for "strongly agree" (or "excellent"). A cumulative score was calculated based on the summed response scores for each item (maximum score = 60). Mean item substitution was used to impute missing data.
Screening Intentions
Screening intentions were also assessed as part of the posttest. Subjects were asked how sure they were that they would schedule an appointment to get screened for colorectal cancer and how sure they were that they would complete the screening test they scheduled. An ordered 5-point response frame was used ranging from 1 for "not at all sure" to 5 for "completely sure".

Full Information

First Posted
November 9, 2005
Last Updated
December 2, 2013
Sponsor
Agency for Healthcare Research and Quality (AHRQ)
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1. Study Identification

Unique Protocol Identification Number
NCT00251862
Brief Title
Shared Decision-Making for Colorectal Cancer Screening
Official Title
Shared Decision-Making for Colorectal Cancer Screening
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Agency for Healthcare Research and Quality (AHRQ)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall objective of this study is to conduct a three-arm randomized controlled trial to evaluate the impact of an interactive, web-based decision aid on shared decision-making and patient adherence to colorectal cancer (CRC) screening recommendations.
Detailed Description
Colorectal cancer (CRC) is the second leading cause of cancer-related death and third most commonly diagnosed cancer among men and women in the United States. Screening has been shown to be a cost-effective strategy for reducing both CRC mortality through early detection and incidence through the detection and removal of precancerous adenomatous polyps (adenomas). Despite a compelling rationale and widespread endorsement by authoritative groups, screening rates remain far below those necessary to achieve significant reductions in CRC mortality or incidence. Poor patient acceptance and non-adherence to screening recommendations are partly responsible for low screening rates. Shared decision-making has been advocated as a potentially effective yet unproven strategy for addressing this problem. Implicit in this approach is the need for an unbiased decision aid that not only educates patients about the pros and cons of the different strategies so as to enable them to identify a preferred strategy but also empowers patients to take a proactive role in the decision-making process, thereby increasing satisfaction and promoting adherence. From a logistical standpoint, the decision aid must also be easy to implement in the ambulatory setting so as to maximize use but minimize demands on physician time and office resources. To address this need, we have developed an interactive, web-based decision aid and implementation strategy for use in routine clinical practice. Comparison(s): Average risk subjects assigned to one of two intervention arms (decision aid alone versus decision aid plus personalized risk assessment with feedback) compared to a control arm(generic website that discusses lifestyle changes that can reduce overall cancer risk).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colorectal cancer screening, Shared decision-making, Decision aid

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
825 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Decision aid plus YourDiseaseRisk
Arm Type
Experimental
Arm Description
Patients viewed the decision aid and completed the Your Disease Risk risk assessment tool prior to visit with their primary care provider.
Arm Title
Decision aid alone
Arm Type
Experimental
Arm Description
Patient's viewed decision aid only prior to a visit with their primary care provider.
Arm Title
III
Arm Type
Sham Comparator
Arm Description
Standard care
Intervention Type
Behavioral
Intervention Name(s)
Web-based decision aid plus personalized risk assessment
Other Intervention Name(s)
Decision aid, personalized risk assessment tool
Intervention Description
Patients review a computer-based decision aid that discuss the pros and cons of of 5 recommended CRC screening options and provides personalized 10-year estimates of CRC risk prior to meeting with their provider to discuss CRC screening.
Intervention Type
Behavioral
Intervention Name(s)
Web-based decision aid alone
Other Intervention Name(s)
Decision aid
Intervention Description
Patients review a computer-based decision aid that discuss the pros and cons of the 5 recommended CRC screening options prior to meeting with their provider to discuss CRC screening.
Intervention Type
Behavioral
Intervention Name(s)
Generic website
Other Intervention Name(s)
Control condtion
Intervention Description
Patients review a generic website that discuss ways to reduce overall cancer risk.
Primary Outcome Measure Information:
Title
Patient Adherence (Test Completion)
Description
Completion of a screening test within 12 months of the study visit.
Time Frame
12 months post-intervention
Secondary Outcome Measure Information:
Title
Patient Knowledge
Description
Knowledge was assessed at baseline (pretest) and at the time of the exit survey (posttest) based on responses to a 12-item questionnaire (True/False/Don't know) that inquired about CRC risk factors, the rationale and goals of screening, and age at which screening should begin. Cumulative knowledge scores (range, 0-12) were derived by summing correct responses to the 12 individual knowledge questions.
Time Frame
Immediate post-intervention study visit
Title
Patient Satisfaction With Decision Making Process
Description
Patient satisfaction with the decision-making process (SDMP) was assessed using the validated 12-item Satisfaction with the Decision-Making Process scale. Five ordered response categories were used for each item. Each response was assigned a point score ranging from 1 for "strongly disagree" (or "poor") to 5 for "strongly agree" (or "excellent"). A cumulative score was calculated based on the summed response scores for each item (maximum score = 60). Mean item substitution was used to impute missing data.
Time Frame
Immediate post-intervention primary care provider (PCP) visit
Title
Screening Intentions
Description
Screening intentions were also assessed as part of the posttest. Subjects were asked how sure they were that they would schedule an appointment to get screened for colorectal cancer and how sure they were that they would complete the screening test they scheduled. An ordered 5-point response frame was used ranging from 1 for "not at all sure" to 5 for "completely sure".
Time Frame
Immediate post-intervention study visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Asymptomatic average-risk subjects Under the direct care of one of participating site's staff (attending) physicians or physician extenders; No prior screening other than fecal occult blood testing (FOBT); No major co-morbidities that preclude CRC screening by any method Exclusion Criteria: Prior CRC screening by any method other than FOBT occult blood testing High-risk condition (personal history of colorectal cancer or polyps, family history of colorectal cancer or polyps involving one or more first degree relatives, chronic inflammatory bowel disease) Lack of fluency in written and spoken English (since decision aid and personalized risk assessment tool will be in English only due to funding issues); Comorbidities that preclude CRC screening by any method
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul C. Schroy III, MD, MPH
Organizational Affiliation
Boston Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
South Boston Community Health Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02127
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18080203
Citation
Schroy PC 3rd, Glick JT, Robinson PA, Lydotes MA, Evans SR, Emmons KM. Has the surge in media attention increased public awareness about colorectal cancer and screening? J Community Health. 2008 Feb;33(1):1-9. doi: 10.1007/s10900-007-9065-5.
Results Reference
background
PubMed Identifier
19933718
Citation
Schroy PC 3rd, Glick JT, Robinson P, Lydotes MA, Heeren TC, Prout M, Davidson P, Wong JB. A cost-effectiveness analysis of subject recruitment strategies in the HIPAA era: results from a colorectal cancer screening adherence trial. Clin Trials. 2009 Dec;6(6):597-609. doi: 10.1177/1740774509346703. Epub 2009 Nov 23.
Results Reference
background
PubMed Identifier
21902773
Citation
Schroy PC 3rd, Mylvaganam S, Davidson P. Provider perspectives on the utility of a colorectal cancer screening decision aid for facilitating shared decision making. Health Expect. 2014 Feb;17(1):27-35. doi: 10.1111/j.1369-7625.2011.00730.x. Epub 2011 Sep 8.
Results Reference
background
PubMed Identifier
20484090
Citation
Schroy PC 3rd, Emmons K, Peters E, Glick JT, Robinson PA, Lydotes MA, Mylvanaman S, Evans S, Chaisson C, Pignone M, Prout M, Davidson P, Heeren TC. The impact of a novel computer-based decision aid on shared decision making for colorectal cancer screening: a randomized trial. Med Decis Making. 2011 Jan-Feb;31(1):93-107. doi: 10.1177/0272989X10369007. Epub 2010 May 18.
Results Reference
result
PubMed Identifier
23159252
Citation
Schroy PC 3rd, Emmons KM, Peters E, Glick JT, Robinson PA, Lydotes MA, Mylvaganam SR, Coe AM, Chen CA, Chaisson CE, Pignone MP, Prout MN, Davidson PK, Heeren TC. Aid-assisted decision making and colorectal cancer screening: a randomized controlled trial. Am J Prev Med. 2012 Dec;43(6):573-83. doi: 10.1016/j.amepre.2012.08.018.
Results Reference
result

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Shared Decision-Making for Colorectal Cancer Screening

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