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Enhancing the Emergency Department Experience for Older Adults: Study Protocol for the Implementation of a Comfort Menu and Cart

Enhancing the Emergency Department Experience for Older Adults: Study Protocol for the Implementation of a Comfort Menu and Cart

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06681376
Enrollment
264
Registered
2024-11-08
Start date
2026-08-01
Completion date
2027-03-10
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comfort, Emergency Department Patient

Keywords

comfort cart, patient experience, older adult, emergency department

Brief summary

Introduction: The aging of the population is a global phenomenon, with projections indicating a significant increase in the proportion of individuals aged 60 years and older by 2050. This demographic shift requires adapting emergency department (ED) services to meet the specific demands of older patients, who often present with multiple comorbidities and face challenges such as sensory and cognitive difficulties. EDs, traditionally designed for acute illness and injury management, may not be adequately equipped to meet the unique needs of this vulnerable population. This can result in suboptimal patient experiences, prolonged ED stays, increased hospitalizations, and poorer outcomes. Methods: This study protocol outlines a before-and-after study to evaluate the impact of implementing a comfort menu and cart on the experience and outcomes of older patients treated in the ED. The study will be conducted in the ED of Hospital Sírio-Libanês (HSL), a tertiary private hospital in São Paulo, Brazil. Patients aged 60 and older who presented to the ED will be eligible for inclusion. Participants will be recruited in two phases: pre-intervention and post-implementation of the comfort menu and cart. Data will be collected through patient and staff interviews, chart reviews, and a 30-day follow-up interview. Patient experience, staff experience, length of hospital stays, hospital costs, ED readmissions, falls, delirium incidence, quality of life, functional status, cognitive performance, and mortality will be assessed. Ethics and dissemination: Ethical approval for this study has been granted by the Institutional Review Board of HSL. All participants, or their legal representatives for those with cognitive impairment, will provide written informed consent before any study procedures are initiated. The consent process has been designed keeping the study hypothesis blind by not revealing the outcomes that will be measured after the comfort cart intervention. The results will be shared with the academic community through peer-reviewed publications and presentations at relevant conferences to inform future clinical practice and research. Expected Results: A positive impact of implementing the comfort menu and cart in the ED is expected on patient-centered outcomes. Improvements in the experience of older patients and medical and multidisciplinary staff are anticipated, and improvements in other exploratory outcomes, such as length of hospital stay, hospital costs, readmissions, falls, delirium incidence, quality of life, functionality, and cognitive performance, will be explored.

Interventions

OTHERComfort menu and cart

The comfort menu and cart will be implemented after the pre-intervention data collection phase is completed. The menu will list the items available on the cart and will be presented to eligible patients in printed or digital format (on a tablet). The cart will be placed in an easily accessible area within the ED. Approximated retail prices have been previously reported. Comfort Cart Contents: * Hot and cold packs; * Extra blanket and pillow; * Face towel; * Gloves and hat; * Personal hygiene kit; * Items for distraction; * Items to enhance communication. Comfort Menu Options: * Physiotherapy assessment; * Conversation with chaplain, concierge, or social worker; * List of resources for older adults needing community services; * Home care assistance.

Sponsors

Hospital Sirio-Libanes
Lead SponsorOTHER
Mayo Clinic
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Masking description

A research assistant, blinded to the initial assessment and ED care details, will conduct a phone interview 30 days (± 2 days) post-initial assessment.

Intervention model description

This study will utilize a quasi-experimental, before-and-after design.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ED attendance at Hospital Sírio-Libanês (HSL), São Paulo, Brazil. * Age ≥ 65 years. * Capacity to consent and respond to the interview or the presence of a companion capable of doing so.

Exclusion criteria

* Decline to participate in the study or use the comfort menu and cart. * Absence of a companion able to consent to study participation and provide necessary information for patients with altered mental status or cognitive impairment. * Decreased level of consciousness. * Hemodynamic instability. * Acute respiratory failure. * Inability to be contacted by phone for the follow-up interview.

Design outcomes

Primary

MeasureTime frameDescription
Experience of older patients treated in the EDBaseline assessment during ED stayLikert scale and brief questionnaire adapted from previous studies

Secondary

MeasureTime frameDescription
Experience of medical and multidisciplinary staff involved in caring for older patients treated in the ED3 months pre- and post-intervention, concurrent with patient inclusionThe interview will follow the standardization of the original comfort cart validation study, using a Likert scale.
Institutional satisfaction indicators30 daysTransactional Net Promoter Score (NPS) and ombudsman manifestations classified as complaints, suggestions, or compliments. Transactional Net Promoter Score (tNPS) is a metric that measures customer loyalty immediately following a specific interaction (e.g., a purchase or support call) rather than the overall brand relationship. It operates on a scale of -100 to +100. Minimum Value (-100): Occurs if 100% of respondents are detractors (rated 0-6) and 0% are promoters (rated 9-10). This indicates severe issues and a high risk of churn. Maximum Value (+100): Occurs if 100% of respondents are promoters (rated 9-10) and 0% are detractors (rated 0-6). This indicates world-class, seamless customer experience.
Caregiver anxiety and depressionBaseline assessment during ED stayAssessed using the Hospital Anxiety and Depression Scale (HADS)
Caregiver burdenBaseline assessment during ED stayAssessed using the Zarit Burden Interview

Countries

Brazil

Contacts

CONTACTPedro K Curiati, M.D., Ph.D.
pedro.kcuriati@hsl.org.br0800 730 2211
PRINCIPAL_INVESTIGATORPedro K Curiati, M.D., Ph.D.

Hospital Sirio-Libanes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026