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NCT Number: NCT07227558

Improving Information Sharing Between Family Caregivers and Home Care Aides

This study will assess the feasibility and acceptability of delivering a home care role and preference guide to up to 50 family caregivers and home care aides of persons living with disability for the purpose of identifying roles between family caregivers and home care aides.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins University

Baltimore, Maryland, 21205, United States

Location status: Recruiting

Location contact

Chanee Fabius, PhD

CONTACT

Valecia Hanna, MS

CONTACT

About this study

This study will assess the feasibility and acceptability of delivering a home care role and preference guide to family caregivers and home care aides of persons living with disability for the purpose of identifying roles between family caregivers and home care aides, as well as preliminary effects on older adult social engagement, caregiver distress, continuity, and feelings of being overwhelmed, family caregiver/direct care worker preparedness, relational coordination, and service satisfaction. The intervention will involve delivering the home care role and preference guide to up to 50 family caregiver-home care care aide dyads to demonstrate the feasibility of collecting primary endpoints relating to older adults' outcomes to be examined in a future ePCT as well as intervention acceptability. Information about family caregivers and home care aide perspectives will be collected at enrollment, 2- and 4-weeks of the intervention.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Home care agency aide:
  • English speaking,
  • home care aides, personal care aides, or personal care aides, providing services to older adults with ADRD.
  • Family or unpaid caregiver eligible for the study if:
  • 18 years and older
  • English speaking
  • hear well enough to communicate by telephone
  • identify themselves as the primary family member or unpaid (friend/companion) caregiver

Exclusion criteria

  • Home care aides are ineligible if:
  • non-English speaking
  • certified nursing assistants, nursing assistant, home health aides, or medication technicians.
  • Family/unpaid caregivers ineligible if:
  • less than 18 years old
  • non-English speaking
  • do not hear well enough to communicate by telephone
  • two or more incorrect answers or not being able to respond to a validated 6-item telephone screening instrument
  • are not identified as the person's primary caregiver, or are paid for services.

Treatment and study plan

GRACE

Other

GRACE- Guide for Role Awareness and Care Engagement is a role and preference guide designed to improve information sharing and clarify role expectations between family caregivers and home care aides of older adults. This guide will outline the various domains of providing care services and preferences for older adults such as daily routine and preferred activities. The intervention will be delivered in-person to the family caregiver and home care aide at the care recipient's home.

Primary outcomes

  1. Acceptability as assessed by survey

    Time frame: 2 week and 4 weeks

    Participants will be asked to rate their overall feedback of the role and preference guide. Participants will be asked how often they used the guide since the last study time point using a scale from 1 to 5 (1=Never, 2=Rarely, 3=Occasionally, 4= Often, 5 Constantly) where higher scores indicate greater frequency of use.

  2. Feasibility as assessed by survey

    Time frame: 2 week and 4 weeks

    Participants will be asked about how helpful the guide was using a scale from 1 to 5:1=Not helpful at all, 2=Not too helpful, 3=Somewhat helpful, 4=Pretty helpful, 5=Very helpful, where higher scores indicate more helpful. More affirmative responses indicate better feasibility of the guide.

  3. Low Social Engagement as assessed by survey question

    Time frame: Baseline, 2 weeks and 4 weeks

    Low social engagement measures an older adult's ability to participate in social activities of longstanding interest reported by the caregiver. This item is measured on a scale from 0-3 (0=Occurred in the last 3 days, 1=Occurred within the last week, 2=Occurred within the last month, 3=Last occurred more than one month ago) where higher scores mean lesser ability to participate in social activities.

  4. Caregiver is Overwhelmed as assessed by survey question

    Time frame: Baseline, 2 weeks and 4 weeks

    Caregivers' feelings of being overwhelmed measures how often a caregiver is overwhelmed by aspects of caregiving responsibilities and older adults' illness. This item is measured using a scale from 1-5 (1=Never, 2=Rarely, 3=Occasionally, 4=Often, 5= Constantly) where higher scores mean greater feelings of being overwhelmed.

  5. Caregiver Distress assessed by survey question

    Time frame: Baseline, 2 weeks and 4 weeks

    Caregivers' feelings of distress measures how often a caregiver is distressed by aspects of caregiving responsibilities and older adults' illness. This item is measured using a scale from 1-5 (1=Never, 2=Rarely, 3=Occasionally, 4=Often, 5= Constantly) where higher scores mean greater feelings of distress.

  6. Caregiver Continuity assessed by survey item

    Time frame: Baseline, 2 weeks and 4 weeks

    Caregivers continuity measures how feelings on inability to continue caregiving. This item is measured using a scale from 1-5 (1=Never, 2=Rarely, 3=Occasionally, 4=Often, 5= Constantly) where higher scores mean greater feelings of distress.

  7. Caregiver Preparedness assessed by The Caregiving Preparedness Scale (CPS)

    Time frame: Baseline, 2 weeks and 4 weeks

    The Caregiving Preparedness Scale (CPS) is an 8-item uni-dimensional instrument that evaluates the extent to which a caregiver and direct care worker feels prepared to meet the psychological and physical needs of a patient (client). The scale was originally developed for family caregivers and has been used to assess caregiver preparedness in direct care workers in prior work. Responses are categorized with a 5-level likert scale: Not at all prepared; not too prepared; somewhat well prepared; pretty well prepared; very well prepared. The total scale score, which is a mean of all items scores, ranges between 0 and 4 with higher score indicating better preparedness.

  8. Relational Coordination assessed by survey

    Time frame: Baseline, 2 weeks and 4 weeks

    Relational coordination suggests that effective coordination occurs through frequent, high-quality communication that is supported by relationships of shared goals, shared knowledge, and mutual respect. Its measurement has been applied across several settings, including home care.

    Family caregivers and direct care workers will rate interactions with each other along three dimensions, with seven questions on a five-point scale related to the components of relational coordination. Four items related to communication include: frequency, timeliness, accuracy, and problem-solving. Three items measured relationships: shared knowledge, goals, and respect for each other. The mean of each of the seven items is calculated for each group (family caregivers and direct care workers). The total score for all items ranges from 7 to 35 where higher scores indicate better coordination and communication among family caregiver and direct care worker.

  9. Direct Care Worker Job Satisfaction assessed by survey question

    Time frame: Baseline, 2 weeks and 4 weeks

    Job satisfaction measures the direct care worker's overall job satisfaction on a scale from 1-4 (1= Very dissatisfied, 2=Dissatisfied, 3=Satisfied, 4=Very Satisfied). Higher score is better.

  10. Number of participants with new Direct Care Worker

    Time frame: 2 weeks and 4 weeks

    Direct Care Worker Turnover measure changes in the enrolled direct care worker participant in the study from the time baseline is completed to study endpoint at 4 weeks. Caregivers will be asked if the direct care worker left and at what time point in the study, and if the participant was assigned or hired a new worker. This will be measured using affirmative responses (yes or no).

Study contacts

Contact information is provided by the study sponsor or research team.

Valecia Hanna, MS

CONTACT

[email protected]

4432202389

Sponsors and collaborators

Lead sponsor

Johns Hopkins Bloomberg School of Public Health

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Improving Information Sharing Between Family Caregivers and Home Care Aides Caring for Persons Living With ADRD

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Nov 12, 2025
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.