Trials Sponsors Conditions Drugs Pricing

Conditions

Dementia

Keywords

surrogate decision-making

Outcome Measures

Primary Outcomes (1)

Feasibility of the I-HTC Checklist EHR Intervention (Reported by Clinicians)
Frequency and proportion of I-HTC use during eligible encounters, clinician activation (accessing the I-HTC at least once), fidelity of ACP and hospice-related EHR documentation, and integration into clinical workflows.
Within 1 month of trial completion

Secondary Outcomes (5)

Usability of the I-HTC Intervention as Reported by Clinicians
Within 1 month of intervention delivery to surrogate
Hospice enrollment of the PLWD
Within 1 month of intervention receipt (PLWD-EHR data)
Surrogate understanding of hospice care
within 1 month of intervention receipt (surrogate)
Surrogate satisfaction
within 1 month of intervention receipt (surrogate)
Quality of communication as reported by the surrogate after receiving the I-HTC intervention
within 1 month of intervention receipt (surrogate)

Study Arms (1)

Usual Care Arm

EXPERIMENTAL

Usual Care Arm: To be used by acute care clinicians with surrogates of eligible hospitalized persons living with dementia

Behavioral: I-HTC

Interventions

I-HTCBehavioral

The I-HTC intervention will include 1) hospice eligibility guide, 2) the I-HTC checklist for hospice communication, and 3) a frequently asked questions (FAQ) guide for clinicians.

Usual Care Arm

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

Clinicians: Physicians, nurse practitioners, physician assistants, nurses, or social workers practicing in acute care; participate in goals-of-care, advance care planning (ACP), hospice, or care transition discussions for hospitalized adults with dementia; and can complete study activities in English; and use the electronic health record for clinical documentation and patience care (EPIC)

Sponsors & Collaborators

Study Sites (1)

NYU Langone Health

New York, New York, 10016, United States

Komal P Murali, PhD, RN, ACNP-BCCONTACT2672055741 kp47@nyu.edu; komal.murali@nyulangone.org

MeSH Terms

Conditions

Dementia

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeurocognitive DisordersMental Disorders

Central Study Contacts

Komal P Murali, PhD, RN, ACNP-BC

CONTACT

267-205-5741 kp47@nyu.edu

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: SUPPORTIVE CARE
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Assistant Professor of Nursing

Study Record Dates

First Submitted

October 15, 2026

First Posted

October 22, 2026

Study Start

December 1, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Primary Completion

June 30, 2027

Inpatient Hospice Transitions Checklist

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (5)

Study Arms (1)

Usual Care Arm

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (5)

Study Arms (1)

Usual Care Arm

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations