RECRUITING

Testing Conversation Aid in Practice

Talk to us

Conditions

Breast CancerMammographyBreast Cancer ScreeningMammography Screening

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this research study is to develop and test a website to help primary care providers (PCPs) discuss the pros and cons of mammography with women aged 75 and older and to help participants make decisions about mammography.

Official Title

Testing a Conversation Aid on Mammography Screening for Clinicians and Women 75 and Older in Practice

Quick Facts

Study Start:2024-05-06
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06011434

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:75 Years to 89 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * English-speaking
  2. * Aged 75 - 89 years
  3. * Seen by an attending-level (non-resident) seen at the recruitment practices who have the -Ability and willingness to provide verbal consent.
  1. * Last mammogram \<6 or \>30 months (so that participants may be contemplative of their next mammogram)
  2. * History of dementia
  3. * Incapacity for informed consent
  4. * History of invasive or non-invasive breast cancer
  5. * Last mammogram was abnormal
  6. * Non-English speaking
  7. * Already chose to stop being screened (documented in medical records or scores of 1-3 \[do not intend to be screened\] on a validate 15 point intentions to be screened scale.)
  8. * PCP unwilling to have patient participate
  9. * In hospice
  10. * PCP not willing to participate
  11. * Psychiatric illness situations that would limit compliance with study requirements

Contacts and Locations

Study Contact

Mara Schonberg, MD, MPH
CONTACT
617-754-1414
mschonbe@bidmc.harvard.edu

Principal Investigator

Mara Schonberg, MD, MPH
PRINCIPAL_INVESTIGATOR
Beth Israel Deaconess Medical Center

Study Locations (Sites)

Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215
United States

Collaborators and Investigators

Sponsor: Beth Israel Deaconess Medical Center

  • Mara Schonberg, MD, MPH, PRINCIPAL_INVESTIGATOR, Beth Israel Deaconess Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-06
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2024-05-06
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • Breast Cancer
  • Mammography
  • Breast Cancer Screening
  • Mammography Screening

Additional Relevant MeSH Terms

  • Breast Cancer