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iCare4Me Transitions

iCare4Me Transitions

Recruiting
18 years and older
All
Phase 3

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Overview

The goal of this randomized controlled trial is to examine the effect of a virtual face-to-face health coach intervention to improve self-care among caregivers of hospitalized older adults during care transitions compared to web-based resource information alone to determine the effectiveness of each intervention. The main questions it aims to answer are:

  1. compare the efficacy of the virtual health coaching intervention vs. web-based information alone in improving self-care in caregivers of hospitalized community-dwelling older adults with multiple chronic conditions (MCCs) who transition from hospital to home,
  2. compare outcomes among Black/African American and White caregivers who receive the intervention vs. digital health information alone, and
  3. explore the estimated the cost of the interventions and acute care resource use among patients of caregivers who received virtual intervention vs. digital health information alone.

Participants who enroll will agree to enroll will:

  • be randomly assigned to either the health information group or the health coaching intervention plus health information group for six months, and
  • be asked to complete a baseline interview, a check-in call at one month post-hospital discharge, and two follow-up interviews at 3- and 6-months after enrollment.

Researchers will compare the two groups of caregivers on the following outcomes: self-care, caregiver self-efficacy (aka confidence), coping, stress, and health status.

Eligibility

Inclusion Criteria:

  • Informal caregiver providing care at least 8 hours/week to the hospitalized older adult (age 65 or older)
  • Reporting poor self-care on screening (Health Self-Care Neglect scale score greater than or equal to 2)
  • Willing to use technology (e.g., computer, smartphone, iPad/tablet)
  • Able to complete the protocol, e.g., adequate vision and hearing
  • English speaking

Exclusion Criteria:

  • Cognitive deficits in orientation and/or recall (Six Item Screener score less than 3)
  • Participation in another similar support or care transition trial
  • Untreated major psychiatric illness (Use of anti-anxiety or anti-depressant medicines is acceptable)

Study details
    Caregiver Stress

NCT06167746

University of Pennsylvania

18 May 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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