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NCT Number: NCT07461168

Penn State Emergency Medicine CarES: Care-partner Evaluation and Sourcing in the Emergency Department

Care partners of people living with dementia often experience ongoing stress and unmet support needs. This study evaluates the feasibility of a low-intensity, supportive education and resource intervention for care partners who previously participated in an observational study.

Participants complete a baseline phone interview and a short stress journaling activity, followed by a six-week series of automated educational and supportive messages delivered by text message or email. Participants may also take part in an optional peer support focus group. The study examines caregiver stress, resilience, engagement with resources, and participant feedback to inform future caregiver support interventions.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Milton S. Hershey Medical Center

Hershey, Pennsylvania, 17033, United States

Location contact

Michelle Fischer, MD, MPH

CONTACT

[email protected]

717-531-1443

Michelle Fischer, MD, MPH

PRINCIPAL_INVESTIGATOR

Rollin Wright, MD, MA, MPH, MS

SUB_INVESTIGATOR

CONTACT

[email protected]

About this study

Care partners of people living with dementia often experience high levels of stress, burden, and unmet support needs, particularly during transitions of care. Even after participating in prior observational research, caregiving demands and stressors may evolve over time, highlighting the need for ongoing education and support.

This is a mixed-methods, minimal-risk interventional study designed to evaluate the feasibility and utility of a low-intensity, supportive education and resource intervention for care partners of people living with dementia. Participants eligible for this study are care partners who previously completed an approved observational study conducted in the emergency department setting.

The study consists of three sequential phases. In the first phase, participants complete a baseline telephone interview assessing caregiver stress, burden, resilience, technology literacy, and caregiving experiences. Participants also complete a brief, structured stress journaling activity over a two-week period to document daily caregiving-related stressors.

In the second phase, participants receive a six-week series of automated educational and supportive messages delivered by text message or email. These messages provide dementia caregiving education, stress and grief management strategies, and links to publicly available caregiver resources. Brief check-in surveys are used to assess participant engagement, perceived usefulness of the materials, and caregiving stressors during this period.

In the final phase, participants are invited to attend an optional, in-person peer support focus group facilitated by trained study personnel. The focus group provides an opportunity for participants to share experiences, discuss caregiving needs, and provide qualitative feedback on the intervention. Sessions are audio recorded for qualitative analysis.

The primary goals of this continuation supplement are to assess the feasibility of delivering supportive educational resources to care partners using low-touch methods, evaluate changes in caregiver stress and resilience, and gather qualitative feedback to inform future caregiver support interventions.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Person completed the CarES Observational Study.
  • Person is a care partner and:
  • Lives with the person living with dementia or
  • Checks on them at least once per week in person or by phone
  • Person is willing and able to participate in study assessments

Exclusion criteria

  • Person is no longer a care partner for a person living with dementia
  • Person declines participation

Treatment and study plan

Care Partner Support and Education Messaging

Behavioral

Care partners receive a low-intensity, supportive intervention consisting of automated educational and supportive messages delivered by text message (SMS) or email over a six-week period. Messages include brief dementia caregiving education, stress and grief management strategies, and links to publicly available caregiving and community support resources. Participants are asked to complete brief check-in surveys to assess engagement, perceived usefulness of the materials, and caregiving stressors.

Primary outcomes

  1. Change in Care Partner Stress

    Time frame: Baseline (prior to intervention) to post-intervention (approximately 6 weeks).

    Caregiver stress will be assessed using the Stress Thermometer, scored from 0 (no stress/distress) to 4 (extreme stress/distress). Higher scores indicate greater stress (worse outcome).

  2. Change In Care Partner Burden

    Time frame: Baseline (prior to intervention) to post-intervention (approximately 6 weeks)

    Caregiver burden will be assessed using the 3-item Zarit Caregiver Burden Interview Screen, calculated as the sum of 3 items, each scored 0-4, for a total score range 0-12 (calculated from item scoring). Higher total scores indicate greater caregiver burden (worse outcome).

Secondary outcomes

  1. Care Partner Resilience (Brief Resilience Scale total score)

    Time frame: Baseline to post-intervention (approximately 6 weeks).

    Care partner resilience will be assessed using the Brief Resilience Scale (BRS). The Brief Resilience Scale total score will be calculated as the mean of 6 items rated on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). Total scores range from 1 to 5, with higher scores indicating greater resilience (better outcome).

Other outcomes

  1. Engagement With Support Resources (check-in survey completion rate)

    Time frame: During the 6-week intervention period

    Participant engagement will be assessed by the proportion of SMS/email check-in surveys completed during the intervention period. Engagement will be calculated as the number of completed check-in surveys divided by the number of surveys sent, expressed as a percentage (0-100%). Higher percentages indicate greater engagement with program communications and support resources.

  2. Perceived usefulness of support resources

    Time frame: During the 6-week intervention period

    Participant-reported usefulness of educational and supportive materials will be assessed using a self-reported usefulness rating collected through check-in surveys. Ratings will be reported on a Likert scale (e.g., 1-5), with higher scores indicating greater perceived usefulness of the materials.

  3. Feasibility of the Support Intervention

    Time frame: Up to 3 months

    Feasibility assessed by participation rates, survey completion rates, and retention across intervention phases.

  4. Qualitative Care Partner Experiences and Feedback

    Time frame: During the intervention period and within 2 weeks following completion of the 6-week intervention

    Qualitative themes related to caregiving experiences, perceived needs, and feedback on the intervention will be identified through semi-structured empathy-focused interviews and peer support focus groups conducted with care partners. Transcripts will be analyzed using qualitative thematic analysis to identify common experiences, perceived benefits, challenges, and suggestions for improving the intervention.

Study contacts

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

Kalen Research Project Manager, MS

CONTACT

[email protected]

Michelle Fischer, MD, MPH

CONTACT

[email protected]

717-531-1443

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Collaborators

  • NYU Langone Health
  • National Institute on Aging (NIA)

Registry information

Official study title

Penn State Emergency Medicine CarES: Care-partner Evaluation and Sourcing in the ED

Acronym: CarES

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 10, 2026
Registry last updated
Jun 15, 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.

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