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Decision-aid on Breast Cancer Screening

Primary Purpose

Breast Cancer

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Decision-aid
Standard information
Sponsored by
Mario Negri Institute for Pharmacological Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer focused on measuring breast cancer screening, mammography, decision-aid, informed choice, National Cancer Screening Program

Eligibility Criteria

45 Years - 69 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women aged 45-69, according to the target age of the screening centres involved;
  • New invited women in mammography screening programme.

Exclusion Criteria:

  • None

Sites / Locations

  • Screening Unit, Cancer Prevention and Research Institute - ISPO
  • UOC Medicina Preventiva delle Comunità - Screening
  • IRCCS-Istituto di Ricerche Farmacologiche Mario Negri
  • U.O. Centro Gestionale Screening, Azienda Sanitaria Provinciale di Palermo
  • Centro Screeening - AUSL Reggio Emilia
  • CPO Piemonte
  • SSD Epidemiologia e Screening - CPO Piemonte - AOU Città della Salute e della Scienza

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Decision-aid

Standard information

Arm Description

Outcomes

Primary Outcome Measures

Number of Participants With Adequate Knowledge
Knowledge will be measured using a questionnaire structured in 13 questions with multiple choice answers, with 2 to 4 options. Ten questions will be qualitative and 3 will be numerical. A score of 8 out of 13 (about 60%) or higher would be considered "adequate knowledge".
Attitude
Attitude will be measured through a scale of 6 items with 5 response options from 1 to 5, with a total score from 6 to 30. The investigators set the threshold for a positive attitude at 24 and consequently the score <24 point a negative attitude.
Intention
Intention will be measured using 1 item with 5 responses: Definitely will, Likely to, Unsure, Not likely to, Definitely will not. The investigators classified "definitely will" and "likely to" as positive intentions.

Secondary Outcome Measures

Participation Rate to the Breast Cancer Screening Programme
Participation rate to the breast cancer screening programme will be assessed as a percentage of participants who actually participate, both in intervention and in the control group.
Satisfaction With the Information Measured Using 8 Items With Three Points Scale
Satisfaction with the given information will be measured using 8 items with three points scale.
Number of Click on the Homepage
Number of click on the Homepage will be assessed trough Pickwick software.
Number of Times Web Platforms Were Accessed
Number of Times Web Platforms were Accessed assessed trough Pickwick software
Number of Pages Visited on the Web Platforms
Number of Pages Visited on the Web Platforms on the web decision aid assessed trough Pickwick software.
Number of Participants With Decisional Conflict Using Decisional Conflict Scale-SURE Version
Decisional conflict will be assessed using the validated and widely used Decisional Conflict Scale-SURE version, consisted in four-item scale.

Full Information

First Posted
March 16, 2017
Last Updated
March 1, 2021
Sponsor
Mario Negri Institute for Pharmacological Research
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1. Study Identification

Unique Protocol Identification Number
NCT03097653
Brief Title
Decision-aid on Breast Cancer Screening
Official Title
New Invited Women to Breast Cancer Screening: a Multi-centre, Longitudinal, Controlled, Randomised Study on a Decision-aid to Support Informed Choice
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
April 20, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mario Negri Institute for Pharmacological Research

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
The present study aim to assess the effect of an interactive web decision aid on informed choice - measured via knowledge, attitudes and intentions concerning breast cancer screening - comparing the decision aid with a standard information provided via web.
Detailed Description
Breast cancer is the most common cancer in women. In Italy, women are invited to a population-based mammography screening programme for the first time at the age of 45 or 50 years. Results from randomised controlled trials, observational studies, and systematic reviews continuously fuel the debate on the balance on benefits (reducing breast cancer mortality) and harms (overdiagnosis, overtreatment) of mammography screening. Physicians, policy makers, as well as laypeople or patient associations agree on the need to inform women about the potential benefits and harms in order to allow an aware decision process. Decision aids are an effective way to support lay people in their decisions about health.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer screening, mammography, decision-aid, informed choice, National Cancer Screening Program

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1001 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Decision-aid
Arm Type
Experimental
Arm Title
Standard information
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Decision-aid
Intervention Description
Web platform with a multilevel information and an aid for the decision to be taken. The content is splitted in 16-20 screens; each screen contains the answer to a common question (i.e. What is mammography screening? What are its benefits and harms? What results can be expected from the participation to mammography screening? What is breast cancer?). The information covers also controversial topics as overdiagnosis, overtreatment and the disagreement among scientists about harms and benefits' quantification.
Intervention Type
Other
Intervention Name(s)
Standard information
Intervention Description
Web platform with a standard brochure. This standard brochure represents a combination of the best information available from the three participate centre' brochures.
Primary Outcome Measure Information:
Title
Number of Participants With Adequate Knowledge
Description
Knowledge will be measured using a questionnaire structured in 13 questions with multiple choice answers, with 2 to 4 options. Ten questions will be qualitative and 3 will be numerical. A score of 8 out of 13 (about 60%) or higher would be considered "adequate knowledge".
Time Frame
7-10 days
Title
Attitude
Description
Attitude will be measured through a scale of 6 items with 5 response options from 1 to 5, with a total score from 6 to 30. The investigators set the threshold for a positive attitude at 24 and consequently the score <24 point a negative attitude.
Time Frame
7-10 days
Title
Intention
Description
Intention will be measured using 1 item with 5 responses: Definitely will, Likely to, Unsure, Not likely to, Definitely will not. The investigators classified "definitely will" and "likely to" as positive intentions.
Time Frame
7-10 days
Secondary Outcome Measure Information:
Title
Participation Rate to the Breast Cancer Screening Programme
Description
Participation rate to the breast cancer screening programme will be assessed as a percentage of participants who actually participate, both in intervention and in the control group.
Time Frame
15-60 days
Title
Satisfaction With the Information Measured Using 8 Items With Three Points Scale
Description
Satisfaction with the given information will be measured using 8 items with three points scale.
Time Frame
7-10 days
Title
Number of Click on the Homepage
Description
Number of click on the Homepage will be assessed trough Pickwick software.
Time Frame
Through study completion, an average of 10 days
Title
Number of Times Web Platforms Were Accessed
Description
Number of Times Web Platforms were Accessed assessed trough Pickwick software
Time Frame
Through study completion, an average of 10 days
Title
Number of Pages Visited on the Web Platforms
Description
Number of Pages Visited on the Web Platforms on the web decision aid assessed trough Pickwick software.
Time Frame
Through study completion, an average of 10 days
Title
Number of Participants With Decisional Conflict Using Decisional Conflict Scale-SURE Version
Description
Decisional conflict will be assessed using the validated and widely used Decisional Conflict Scale-SURE version, consisted in four-item scale.
Time Frame
7-10 days

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women aged 45-69, according to the target age of the screening centres involved; New invited women in mammography screening programme. Exclusion Criteria: None
Facility Information:
Facility Name
Screening Unit, Cancer Prevention and Research Institute - ISPO
City
Firenze
Country
Italy
Facility Name
UOC Medicina Preventiva delle Comunità - Screening
City
Milan
ZIP/Postal Code
20122
Country
Italy
Facility Name
IRCCS-Istituto di Ricerche Farmacologiche Mario Negri
City
Milan
ZIP/Postal Code
20156
Country
Italy
Facility Name
U.O. Centro Gestionale Screening, Azienda Sanitaria Provinciale di Palermo
City
Palermo
Country
Italy
Facility Name
Centro Screeening - AUSL Reggio Emilia
City
Reggio Emilia
ZIP/Postal Code
42122
Country
Italy
Facility Name
CPO Piemonte
City
Torino
Country
Italy
Facility Name
SSD Epidemiologia e Screening - CPO Piemonte - AOU Città della Salute e della Scienza
City
Torino
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
28629329
Citation
Roberto A, Colombo C, Candiani G, Giordano L, Mantellini P, Paci E, Satolli R, Valenza M, Mosconi P. Personalised informed choice on evidence and controversy on mammography screening: study protocol for a randomized controlled trial. BMC Cancer. 2017 Jun 19;17(1):429. doi: 10.1186/s12885-017-3428-9.
Results Reference
background
PubMed Identifier
32546834
Citation
Roberto A, Colombo C, Candiani G, Satolli R, Giordano L, Jaramillo L, Castagno R, Mantellini P, Falini P, Carnesciali E, Valenza M, Costa L, Campari C, Caroli S, Faggiano RC, Orione L, Belmessieri B, Marchio V, Deandrea S, Silvestri A, Luciano D, Paci E, Mosconi P. A dynamic web-based decision aid to improve informed choice in organised breast cancer screening. A pragmatic randomised trial in Italy. Br J Cancer. 2020 Sep;123(5):714-721. doi: 10.1038/s41416-020-0935-2. Epub 2020 Jun 17. Erratum In: Br J Cancer. 2021 Jul;125(1):146-147.
Results Reference
result

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Decision-aid on Breast Cancer Screening

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