DECAD: Decisions About Cancer Screening in Alzheimer's Disease

Sponsor
Indiana University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03282097
Collaborator
(none)
426
5
2
85.5
85.2
1

Study Details

Study Description

Brief Summary

The Decisions about Cancer screening in Alzheimer's Disease (DECAD) study is the first study to test if an evidence-based decision aid for AD caregivers can support decision-making about mammography and improve the quality of medical decision-making about breast cancer screening. This large randomized controlled trial will recruit up to 450 dyads (900 individual participants) of older women with AD and a family caregiver, for a goal of 426 dyad baselines (852 individual participants), from 24 primary care practices in central Indiana to test this decision aid.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: DECAD decision aid
  • Other: Home safety guide
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
426 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Decisions About Cancer Screening in Alzheimer's Disease
Actual Study Start Date :
Nov 17, 2017
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mammogram decision aid

Will be mailed the DECAD decision aid before their next PCP visit in order to better inform their decision to continue or stop mammography.

Behavioral: DECAD decision aid
A mammography decision aid that will help caregivers of patients with Alzheimer's make decisions about stopping or continuing breast cancer screening.

Active Comparator: Home safety guide

The home safety guide is a two-page paper pamphlet developed by the American Geriatrics Society Foundation for Health in Aging. It provides tips about important actions older adults can take to prevent falls, poisoning, and bathroom hazards and protection against abuse, fire and other related hazards. We selected the home safety guide to account for the attention given to the intervention group but not to provide information that would bias the control group away from talking about mammography with the patient's PCP.

Other: Home safety guide
The home safety guide provides tips about important actions older adults can take to prevent falls, poisoning, and bathroom hazards and protection against abuse, fire and other related hazards.
Other Names:
  • control group
  • Outcome Measures

    Primary Outcome Measures

    1. Decisional conflict Scale [0-5 days after the POST-Index PCP visit]

      The DCS includes 16 questions regarding a medical decision that they have made or that they are about to make. It is a validated and widely accepted measure of decision quality that has been used in previous studies of decision aids intended for AD caregivers

    Secondary Outcome Measures

    1. Change in Decision-making self-efficacy [Baseline and 0-5 days after the POST-Index post PCP visit]

      To measure decision-making self-efficacy, we will use the Decision Self-Efficacy Scale (DSE). The DSE is a validated, 11-item instrument that measures how confident the respondent is in their ability to make an informed medical decision, including SDM. We will adapt the DSE with five response categories ("not at all confident" to "very confident") to measure caregiver decision-making self-efficacy for mammography decisions for their relative with AD.

    2. Caregiver Role in decision making [0-5 days after the PCP Index visit]

      Adapted from the Control Preferences Scale, this is a 4-item instrument to assess preferences for and involvement in making decisions on their own or sharing responsibility with the patient or doctor.

    3. Patient Role in decision making [0-5 days after the PCP Index visit]

      Adapted from the Control Preferences Scale, this is a 2-item instrument to assess involvement in making decisions on their own or sharing responsibility with their family or doctor.

    4. Record of mammogram [15 month followup, 24 month EMR data]

      We will ask caregivers at the 15 months post-intervention follow-up, via phone-administered questionnaire, if the patient received a mammogram at any time since intervention date and any burdens of the procedure for the patient or for them. We will also review the patient's EMR to assess primary care notes, radiology records, and other documentation of a mammogram outside of the INPC at the 24 months post-intervention follow-up.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    75 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Patient Inclusion Criteria:
    • Female and 75 years or older

    • At least one mammogram in the past five years

    • Primary care visit scheduled in the next 12 months

    • Diagnosis of Alzheimer's disease or related dementia as determined by ICD-10 code

    • Ability to provide informed consent or assent

    • Ability to communicate in English

    Patient Exclusion Criteria:
    • Permanent resident of a nursing facility

    • Had a mammogram in the past 6 months

    • Primary care visit scheduled is the first visit with the PCP

    • Made a decision to stop getting mammograms

    • History of Atypical Ductal Hyperplasia, lobular carcinoma in situ, ductal carcinoma in situ, or non-invasive breast cancer

    • Has mild cognitive impairment, serious mental illness such as bipolar or schizophrenia as determined by ICD-10 code

    Caregiver Inclusion Criteria:
    • 18 years or older

    • Primary family caregiver of the patient*

    • Must have a telephone

    • Ability to provide informed consent

    • Ability to communicate in English

    Caregiver Exclusion Criteria:
    • Caregiver is a non-family member who is not a legal Healthcare Power of Attorney

    • Less than a 7th grade education**

    • Made a decision that the patient will stop getting mammograms

    • Has a diagnosis of AD or has a serious mental illness such as bipolar or schizophrenia as determined by ICD-10 code

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Parkview Health Fort Wayne Indiana United States 46805
    2 Alzheimer's Association Indianapolis Indiana United States 46220
    3 Eskenazi Health Indianapolis Indiana United States 46220
    4 IU Health Indianapolis Indiana United States 46220
    5 Beth Israel Deaconess Medical Center Boston Massachusetts United States 02215

    Sponsors and Collaborators

    • Indiana University

    Investigators

    • Principal Investigator: Nicole Fowler, PhD, Indiana University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nicole R. Fowler, PhD, Assistant Professor of Medicine, Indiana University
    ClinicalTrials.gov Identifier:
    NCT03282097
    Other Study ID Numbers:
    • 1501278953
    First Posted:
    Sep 13, 2017
    Last Update Posted:
    Aug 17, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 17, 2022