Development, Implementation and Evaluation of an Individual Decision Aid in Swedish Cancer Screening Programs (BESTa)
Primary Purpose
Neoplasm, Colorectal, Neoplasm, Breast, Neoplasm, Ovarian
Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Individual decision aid (iDA)
Sponsored by
About this trial
This is an interventional screening trial for Neoplasm, Colorectal focused on measuring Decision Support Techniques, Shared, Decision Making, Health promotion, Early detection of cancer
Eligibility Criteria
Inclusion Criteria:
- women aged 23 -74
- men aged 60 - 74
Exclusion Criteria:
- none
Sites / Locations
- Karolinska InstitutetRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Women aged 23 -74 and men aged 60 - 74 invited to population based cancer screening
Arm Description
Women aged 23 -74 targeted for breast cancer, cervical and bowel screening and men aged 60-74 targeted for bowel screening will be invited to the project. Efforts will be made to recruit participants who normally do not participate in research and screening, such as those with various disabilities, participants who live outside society and foreign born.
Outcomes
Primary Outcome Measures
Comprehensibility regarding iDA content
The iDA will be evaluated for its content using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Usability regarding iDA format
The iDA will be evaluated for its usability using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Feasibility regarding iDA format
The iDA will be evaluated for its feasibility using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Secondary Outcome Measures
Self-reported knowledge of cancer and screening
Knowledge of cancer and screening of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Self-reported attitudes and preferences to cancer screening
Attitudes and preferences to screening of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Self-reported lifestyle behaviors
Lifestyle behaviors, such as physical activity, food intake, smoking and alcohol of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Full Information
NCT ID
NCT05512260
First Posted
June 30, 2022
Last Updated
March 9, 2023
Sponsor
Karolinska Institutet
Collaborators
Jonkoping University, Malmö University, Umeå University, Leiden University, Dalarna University, Karolinska University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05512260
Brief Title
Development, Implementation and Evaluation of an Individual Decision Aid in Swedish Cancer Screening Programs
Acronym
BESTa
Official Title
Towards High, Equal and Informed Participation in Swedish Cancer Screening - the BESTa Project.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Jonkoping University, Malmö University, Umeå University, Leiden University, Dalarna University, Karolinska University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Sweden has a long tradition of organized national population-based screening programs. Participation rates differ between programs and regions, are relatively high in some groups, but lower in other. To apply an equity perspective on screening, it is desired that individuals make an informed decision on knowledge rather than ignorance, misconceptions, or fear. Decision Aids (DAs) are set to deliver information about different health care options and to help individuals make visible values connected to the options available. DAs are not meant to guide individuals to choose one option over the another. The advantage of an individual Decision Aid (iDA) is that individuals gain knowledge on cancer and screening entering one webpage with possibility to communicate with health professionals and thereafter make their decision regarding participate. The primary objective is therefore to develop and implement a web-based iDA for individuals invited to cancer screening in Sweden. The secondary objective is to evaluate the implemented web-based iDA.
Methods: This study has an evaluative approach with both a process-, an implementation and an outcome evaluation. Multiple methods will be used including patient reported data, focus group discussions and individual interviews using the think aloud technique. The project is based on the framework from The International Patient Decision Aid Standards (IPDAS) and the proposed model development process for DAs as presented by Coulter et al. Individuals aged 23-74, including women aged (the cervical- and breast- and bowel cancer screening module) and men aged (the bowel cancer screening module), will be included in the developmental process. Efforts will be made to recruit participants with disabilities, who live outside society and who are foreign born.
Discussion: To the best of our knowledge the present study is the first aiming at developing an iDA for usage in Swedish context, The iDA is intended to contribute so that individuals invited to screening base their decision on knowledge and with a clear picture of their values and preferences, rather than ignorance, misconceptions, or fear. Furthermore, the iDA is expected to increase knowledge and raise awareness in general about cancer and cancer screening in society.
Detailed Description
INTRODUCTION AND RATIONALE For cancer screening programs to be effective, a high willingness from seemingly healthy individuals to participate is a prerequisite. Participation rates differ and are relatively high in some population groups but at the same time low in other groups. It is well known that individuals with lower socioeconomic status, ethnic minorities and individuals with disabilities participate to a limited extent in cancer screening. A decision aid (DA) is set to deliver information about different health care options and to help individuals make their values visible connected to the options available. Using a DA in connection to cancer screening can increase participation based on knowledge rather than misconception or fear.
The present project is based on the theoretical framework of shared decision making (SDM), with the overarching goal to improve the quality of health care decisions. SDM in this project is based on the work of Charles and Gafni with three cornerstones important for the decision-making process: information/knowledge - to make an informed decision persons need information to gain knowledge about e.g., pros and cons; Values/preferences - persons process their options in relation to attitudes and behaviors; and Involvement - of both the individual and health care professionals.
To date, no DA for any of the screening programs exist in Sweden why this project is warranted. By designing the communication strategies in various ways, regarding information about screening options, and to help individuals construct, clarify and communicate personal values, the researchers intention is to support the decision-making process and to address and acknowledge the equity perspective.
METHODS
Phase 1
Design This study has an evaluative approach encompassing both a process-, an implementation and an outcome evaluation. Multiple methods will be used to answer the research questions including patient reported data, focus group discussions and individual interviews using the think aloud technique. The project is based on the framework from IPDAS and the proposed model development process for DAs, as presented by Coulter et al.
Procedure and outcomes
The procedure will follow the model development process for DAs, applying the following steps:
Define scope - a description of breast, cervix and bowel cancer including screening will be formulated, information will be gathered regarding treatment, screening tests, true positive true negative results, risks, and benefits with screening vs. non-screening and detection probabilities. The target audience is all individuals invited to cancer screening.
Steering group - a multidisciplinary group will be formed with stakeholders: lay people (aged 23-74), different socioeconomic status and ethnicity, from urban and rural areas, invited to and not invited to screening); clinical experts (oncologists, endoscopists, gastroenterologist, gynecologists, registered nurses, psychologists) and other experts (in psychometry and IT); collaboration partners (The Swedish Association of Local Authorities and Regions - SKR, Regional Cancer Centers - RCC, National Board of Health and Welfare). No disclosed declaration of interest.
Design - provision of the iDA in paper format, i.e., a version with the tentative content, including the research and evidence that the iDA is based on as well as a description of the prototype development. The design of the paper version is inspired by the work of Schwartz and colleagues and will be evaluated by lay persons and experts for its content and comprehensibility regarding format (information and descriptions in text and images) and language use.
Alpha testing - the web-based iDA will be evaluated for its content, comprehensibility, usability and feasibility, regarding format (information and descriptions in text, spoken animations, images, audio, animated videos, certain clickable words to provide additional information, and interactive questions to help individuals to clarify and express values); language use; setting (web-based) and timing (open for anyone, link will be provided with the invitation).
Beta testing - the iDA will be tested in a "real world setting" and evaluated regarding format (information and descriptions in text, spoken animations, images, audio, animated videos, certain clickable words to provide additional information, and interactive questions to help individuals to clarify and express values); language use; setting (web-based) and timing (open for anyone, link will be provided with the invitation).
Data collection During the steps 3-5 data will be collected using different qualitative methods. Data regarding content, format, language use, setting and timing will be generated from focus group discussion and individual interviews. An interview guide with opened-ended questions and optional probe questions will guide the data collection. Participants will be able to choose to participate in a focus group discussion or an individual interview.
During step 3, data regarding the questions, including interactive questions (values and preferences, knowledge, and lifestyle exercises) (step 4) will be generated from concurrent cognitive interviewing where the individual gives a verbal account of their thinking while responding to the interactive questions included in the iDA. The interviews will follow a "think aloud" protocol where individuals are asked to respond to the interactive questions and encouraged to think out loud and to verbalize their thoughts while doing so. This gives an understanding on the perception of each question, as the participants work themselves through the content. In addition, probing questions will be asked when changes in appearance, such as frowning or hesitation occurs and when, or if, the session leader needs further clarification.
Data management Demographic data will be pseudo anonymized, meaning that all personal names will be removed during transcription and all participants in the studies will be given a unique code. A code list will not be established since no personal data is handled. All data will be storage in a secured facility at the Division of Nursing, Karolinska Institutet according to regulations at the university.
Data analyses Data generated from focus group discussions and individual interviews will be analyzed using descriptive and manifest content analysis. Data generated from cognitive interviews applying the "think aloud" method will be compiled and organized according to responses.
Phase 2
Procedure and outcomes After the beta-testing the iDA will be public and accessible for all who are invited and/or interested in the cancer screening programs. To be able to evaluate and develop the iDA further, topics such as digital health literacy, knowledge, values and preferences, decisional conflict, concerns, and risk awareness will be studied with self-reported questions. In addition, demographic questions such as sex, age, educational level, employment will be included as well as questions regarding lifestyle and physical activity. Usability of the iDA including the chat function, helpline, and behavior flow, i.e., how individuals navigate in the iDA will also be scrutinized.
Data collection Data will be collected through self-reported questions included in the iDA.
Data management Questionnaire data will be stored in the web-platform owned by RCC. Extracted data will be pseudo anonymized, meaning that all proper names will be removed during transcription and all participants in the studies will be given a unique code. A code list will not be established since no personal number will be handled. All data will be storage in a secured facility at the Division of Nursing, Karolinska Institutet according to regulations at the university.
Data analyses Data will be analyzed and compared using relevant descriptive and inferential statistics.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasm, Colorectal, Neoplasm, Breast, Neoplasm, Ovarian
Keywords
Decision Support Techniques, Shared, Decision Making, Health promotion, Early detection of cancer
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
220 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Women aged 23 -74 and men aged 60 - 74 invited to population based cancer screening
Arm Type
Other
Arm Description
Women aged 23 -74 targeted for breast cancer, cervical and bowel screening and men aged 60-74 targeted for bowel screening will be invited to the project. Efforts will be made to recruit participants who normally do not participate in research and screening, such as those with various disabilities, participants who live outside society and foreign born.
Intervention Type
Device
Intervention Name(s)
Individual decision aid (iDA)
Other Intervention Name(s)
Decision aid in paper format
Intervention Description
A web-based iDA (accessible online with various content), will be developed towards individuals approached to cancer screening, although public and accessible to all who are interested in cancer and screening. DAs in screening usually include information on the disease, screening, screening tests, benefits and harms and some value clarification exercise (e.g., interactive questions) aiming at shedding light on the individual´s values and preferences, knowledge and lifestyle.
Primary Outcome Measure Information:
Title
Comprehensibility regarding iDA content
Description
The iDA will be evaluated for its content using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Time Frame
up to 10 months
Title
Usability regarding iDA format
Description
The iDA will be evaluated for its usability using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Time Frame
up to 10 months
Title
Feasibility regarding iDA format
Description
The iDA will be evaluated for its feasibility using qualitative methods such as individual interviews, focus group discussions and cognitive interviewing
Time Frame
up to 10 months
Secondary Outcome Measure Information:
Title
Self-reported knowledge of cancer and screening
Description
Knowledge of cancer and screening of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Time Frame
up to 12 months
Title
Self-reported attitudes and preferences to cancer screening
Description
Attitudes and preferences to screening of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Time Frame
up to 12 months
Title
Self-reported lifestyle behaviors
Description
Lifestyle behaviors, such as physical activity, food intake, smoking and alcohol of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Time Frame
up to 12 months
Other Pre-specified Outcome Measures:
Title
Satisfaction with the iDA and the decision
Description
Satisfaction with the iDA and the decision of iDA users will be evaluated with self-reported questions including response options such as yes/no/do not know
Time Frame
up to 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
23 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
women aged 23 -74
men aged 60 - 74
Exclusion Criteria:
none
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kaisa Fritzell, PhD
Phone
+46761407424
Email
kaisa.fritzell@ki.se
First Name & Middle Initial & Last Name or Official Title & Degree
Anna Jervaeus, Docent
Phone
+46702642039
Email
anna.jervaeus@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kaisa Fritzell, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institutet
City
Huddinge
ZIP/Postal Code
14152
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kaisa Fritzell, Phd
Phone
+46812378374
Email
kaisa.fritzell@ki.se
First Name & Middle Initial & Last Name & Degree
Anna Jervaeus, Ass professor
Phone
+46702642039
Email
anna.jervaeus@ki.se
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data will be shared upon request
Citations:
PubMed Identifier
24645693
Citation
Charles C, Gafni A. The vexing problem of defining the meaning, role and measurement of values in treatment decision-making. J Comp Eff Res. 2014 Mar;3(2):197-209. doi: 10.2217/cer.13.91.
Results Reference
background
PubMed Identifier
16908462
Citation
Elwyn G, O'Connor A, Stacey D, Volk R, Edwards A, Coulter A, Thomson R, Barratt A, Barry M, Bernstein S, Butow P, Clarke A, Entwistle V, Feldman-Stewart D, Holmes-Rovner M, Llewellyn-Thomas H, Moumjid N, Mulley A, Ruland C, Sepucha K, Sykes A, Whelan T; International Patient Decision Aids Standards (IPDAS) Collaboration. Developing a quality criteria framework for patient decision aids: online international Delphi consensus process. BMJ. 2006 Aug 26;333(7565):417. doi: 10.1136/bmj.38926.629329.AE. Epub 2006 Aug 14.
Results Reference
background
PubMed Identifier
24625093
Citation
Coulter A, Stilwell D, Kryworuchko J, Mullen PD, Ng CJ, van der Weijden T. A systematic development process for patient decision aids. BMC Med Inform Decis Mak. 2013;13 Suppl 2(Suppl 2):S2. doi: 10.1186/1472-6947-13-S2-S2. Epub 2013 Nov 29.
Results Reference
background
PubMed Identifier
33813928
Citation
Schwartz PH, O'Doherty KC, Bentley C, Schmidt KK, Burgess MM. Layperson Views about the Design and Evaluation of Decision Aids: A Public Deliberation. Med Decis Making. 2021 Jul;41(5):527-539. doi: 10.1177/0272989X21998980. Epub 2021 Apr 5.
Results Reference
background
PubMed Identifier
12641812
Citation
Drennan J. Cognitive interviewing: verbal data in the design and pretesting of questionnaires. J Adv Nurs. 2003 Apr;42(1):57-63. doi: 10.1046/j.1365-2648.2003.02579.x.
Results Reference
background
PubMed Identifier
16204405
Citation
Hsieh HF, Shannon SE. Three approaches to qualitative content analysis. Qual Health Res. 2005 Nov;15(9):1277-88. doi: 10.1177/1049732305276687.
Results Reference
background
PubMed Identifier
26680216
Citation
Essink-Bot ML, Dekker E. Equal access to colorectal cancer screening. Lancet. 2016 Feb 20;387(10020):724-6. doi: 10.1016/S0140-6736(15)01221-0. Epub 2015 Dec 9. No abstract available.
Results Reference
background
PubMed Identifier
26715453
Citation
Zidar MN, Larm P, Tillgren P, Akhavan S. Non-attendance of mammographic screening: the roles of age and municipality in a population-based Swedish sample. Int J Equity Health. 2015 Dec 30;14:157. doi: 10.1186/s12939-015-0291-7.
Results Reference
background
Links:
URL
http://journals.library.brocku.ca/brocked/index.php/home/article/view/38
Description
The use of think-aloud methods in qualitative research an introduction to think-aloud methods.
URL
http://ipdas.ohri.ca/
Description
International Patient Decision Aid Standards IPDAS.
Learn more about this trial
Development, Implementation and Evaluation of an Individual Decision Aid in Swedish Cancer Screening Programs
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