FACT-AD: Families Coping Together With Alzheimer's Disease

Sponsor
Yale University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04642885
Collaborator
National Institute on Aging (NIA) (NIH), National Institutes of Health (NIH) (NIH), Department of Health and Human Services (U.S. Fed)
50
1
36
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Study Details

Study Description

Brief Summary

Two remote phone/zoom calls are required to assess experiences as a family coping with dementia.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Using a combination of paper or online surveys in addition to interactive visits with blood pressure monitoring, participants are observed interacting with each other. Blood pressure devices are mailed to their homes and only worn for six minute intervals. The first visit generally lasts one hour and the second visit 90 minutes.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    50 participants
    Observational Model:
    Family-Based
    Time Perspective:
    Prospective
    Official Title:
    Families Coping Together With Alzheimer's Disease
    Actual Study Start Date :
    Jun 30, 2019
    Anticipated Primary Completion Date :
    Jun 30, 2022
    Anticipated Study Completion Date :
    Jun 30, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    dyad

    parent with dementia and an adult child who is a caregiver

    Outcome Measures

    Primary Outcome Measures

    1. Caregiver demand appraisals [Baseline and one year]

      (1a) Caregiver demand appraisals: 6 items from the 12-item Zarit Burden Interview (ZBI) will assess caregiver appraisals of demands (e.g., That because of the time you spend with your relative that you don't have enough time for yourself?". Caregivers self-report aspects of burden on a scale from 0 (never) to 4 (nearly always; α= .86). Higher numbers indicate higher demands. Administration is 2.5 minutes

    2. Caregiver perceived stress [Baseline and one year later]

      (1b) Caregiver perceived stress: 6 items from the 12-item Zarit Burden Interview (ZBI) will assess caregiver perceived stress (e.g., "Stressed between caring for your relative and trying to meet other responsibilities (work/family)?"). Caregivers self-report aspects of burden on a scale from 0 (never) to 4 (nearly always; α= .86). Higher numbers indicate higher stress. Administration is 2.5 minutes.

    3. Caregiver negative Coping [Baseline and one year later]

      The Brief COPE Inventory is a shortened version (28 items) of the COPE inventory in which respondents indicate how often they use a particular coping strategy under stress as ranked on a 4-point scale with 1 (I haven't been doing this at all) to 4 (I've been doing this a lot). Examples of items include "I've been using alcohol or drugs to help me get through it." and "I've been criticizing myself" (α=0.72, 0.84, 0.75 for emotion, problem, and dysfunction focused subscales). Higher scores indicate poorer coping. Administration is 10 minutes

    Secondary Outcome Measures

    1. Relational Functioning [Baseline and one year later]

      The Relationships Inventory will measure the degree to which individuals perceive that they can rely on their parent or child for help and support when needed (e.g., "to what extent can you count on your parent/child for help with a problem?" "to what extent can you count on your parent/child to give you honest feedback, even when you might not want to hear it?"). Ratings will be made on a scale from 1 (not at all) to 5 (very much; α=.79). Four additional items will assess the degree to which individuals perceive that their parent/child is a good support-provider (e.g., "overall, my parent/child is a good support-provider" using a scale from 1 (strongly disagree) to 7 (strongly agree). Higher numbers indicate higher relationship functioning. Administration is 5 minutes.

    2. Health [Baseline and one year later]

      Health-related quality of life will be assessed using the 12-item Short Form Survey (SF-12) version 1.0, documenting the extent of limitations in a number of domains. Higher scores indicate better physical and mental health-related quality of life. It has been used with both persons with ADRD and caregivers. Administration is 5 minutes. The minimum and maximum scores are 0 and 100.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Parent must be 55 plus with symptoms or a diagnosis of dementia

    • Adult child must be over 18 and involved in some way with assisting parent.

    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Yale school of Public Health New Haven Connecticut United States 06511

    Sponsors and Collaborators

    • Yale University
    • National Institute on Aging (NIA)
    • National Institutes of Health (NIH)
    • Department of Health and Human Services

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yale University
    ClinicalTrials.gov Identifier:
    NCT04642885
    Other Study ID Numbers:
    • 2000024219
    • R01AG058565
    First Posted:
    Nov 24, 2020
    Last Update Posted:
    Oct 15, 2021
    Last Verified:
    Oct 1, 2021
    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 Oct 15, 2021