Improving Palliative Care Access Through Technology

NCT ID: NCT04969484

Last Updated: 2021-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

SUSPENDED

Clinical Phase

NA

Total Enrollment

81 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-19

Study Completion Date

2022-06-30

Brief Summary

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This project will focus on developing, optimizing and pilot-testing a multi-component Improving Access Through Technology (ImPAcTT) intervention that leverages existing telehealth technologies to provide staff education; family outreach, engagement and support; care coordination; and resident symptom management and facilitation of goals-of-care discussion.

Detailed Description

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Almost 1.8 million older Americans live in nursing homes (NH), with estimates that this number will grow to more than 3 million by 2050. NHs are increasingly becoming the place of care and site of death for frail older adults dying from multiple chronic illnesses. Unfortunately, most residents die without the benefit of palliative care (PC) or with palliation delayed until the last days of life.

Unfortunately, hospice services are often the only formal end of life care service available in NHs, and access to hospice enrollment is complicated by financial implications for both NHs and residents.

Telehealth, or remote monitoring of patients through information and communication technologies, is an effective mechanism for addressing the increased demand on health services and has much to offer to people living with and dying from advanced illness. Moreover, numerous studies have demonstrated positive benefits of using telehealth in the NH to improve access to consultants (e.g., neurology, dermatology, psychiatry).

Little is known, however, about the effect of using Telehealth on improving access to PC specialists in the NH setting.

The proposed ImPAcTT intervention employs a secure communications platform that permits multi-person live video, audio, and text message consultations; real-time document sharing and documentation for advanced care planning discussions; and remote virtual assessment capabilities.

The investigator will conduct a pilot implementation trial of ImPAcTT in 3 study nursing homes to evaluate our ability to safely recruit and retain study participants, collect appropriate and accurate data, and determine preliminary estimates of an effect size of the intervention.

Conditions

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Telehealth Palliative Care

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

The trial will be implemented in 3 nursing homes to evaluate the feasibility and acceptability of the multi-component ImPAcTT intervention.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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ImPAcTT intervention

Within 48-72 hours of enrollment in the study, the primary participant and family will receive an ImPAcTT Telehealth visit with the PC provider. The provider will conduct a comprehensive PC assessment aligned with the National Consensus Project for Quality Palliative Care guidelines. Visits, which may include remote physical assessment using a digital stethoscope, dermatoscope, etc., will be documented and transmitted to the NH. Advanced Care Planning (ACP) and goals of care discussions will be facilitated by the ability to virtually share and edit documents, such as the Physician Orders for Life Sustaining Treatment (POLST), in real time with primary participants and/or family. The PC provider will conduct follow-up visits 1 week following the initial visit, then on a case-by-case basis.

Group Type EXPERIMENTAL

Telehealth visit

Intervention Type OTHER

ImPACTT Telehealth visit with the PC provider

Usual care

Participants will receive the standard of care established at the NH.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Telehealth visit

ImPACTT Telehealth visit with the PC provider

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Primary participant

* Age \>= 18 years
* English language fluency
* Palliative Care Consult Screening Tool (PCCS) scoring 9 or above
* If participant does not demonstrate capacity to consent, he/she must be able to assent to study procedures, be told of plan to approach surrogate and have a legally authorized representative available to provide consent

Family/friend caregivers:

* Closest relative/next of kin/friend who is involved in the care of his/her loved one before and during the study period
* English fluency

Exclusion Criteria

Primary participant:

* Enrolled in hospice
* Unable to assent to study procedures
* Expresses resistance or dissent to participation or the use of surrogate consent

Family/friend caregiver:

* Life expectancy \< 1 year (e.g., metastatic cancer)
* Evidence of cognitive impairment or inability to consent to study procedures
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Aging (NIA)

NIH

Sponsor Role collaborator

University of Utah

OTHER

Sponsor Role lead

Responsible Party

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Caroline Stephens

PhD, RN, GNP-BC, FAAN, Helen Lowe Bamberger Colby Presidential Endowed Chair in Gerontological Nursing, Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Caroline E Stephens, PhD, RN

Role: PRINCIPAL_INVESTIGATOR

University of Utah

Locations

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University of California San Francisco - UCSF

San Francisco, California, United States

Site Status

University of Utah

Salt Lake City, Utah, United States

Site Status

Countries

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United States

References

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Related Links

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https://www.capc.org/capc-reports-and-publications/

Improving palliative care in nursing homes \[online report\]. New York: Center to Advance Palliative Care. 2008.

https://us.sagepub.com/en-us/nam/basics-of-qualitative-research/book235578

Corbin J, Strauss A, Strauss AL. Basics of qualitative research. Sage; 2014.

Other Identifiers

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5K76AG054862-05

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IRB_00129094

Identifier Type: -

Identifier Source: org_study_id

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