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Healthy AgingEPICNCT05381480

Elders Preserving Independence in the Community

A study testing In-home Preventive Health Visits by Advanced Practice Nurse and On-site Evidence-based Physical Activity, Health and Wellness Classes in people with Healthy Aging, run by Cedars-Sinai Medical Center at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

Twenty percent of the US population will be age 65 or older by 2050, a surge from 8 percent in 1950 and 12 percent in 2000. The proportion of low-income older adults is also growing. Read more about this study

Who is it for?
Ages 55 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy Aging
What is being tested?
In-home Preventive Health Visits by Advanced Practice Nurse and On-site Evidence-based Physical Activity, Health and Wellness Classes
Could I receive a placebo?
No, everyone receives an active treatment
How many people
104 participants
Where
1 siteUnited States
Study dates
22 Nov 2022to 30 Sep 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 55 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age and income qualified tenants in 18 identified older adult low income independent living apartment buildings.

Who cannot join

  • Non-tenants in 18 identified buildings
  • Assessed to be cognitively impaired and unable to consent.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Cedars-Sinai Medical Center

    Los Angeles, California, 90048

Other trials in United States

About this study

Twenty percent of the US population will be age 65 or older by 2050, a surge from 8 percent in 1950 and 12 percent in 2000. The proportion of low-income older adults is also growing. Approximately 70 percent of people 65 and older are expected to need some level of long-term care, which may burden the nation's health and caregiver systems. While there are many models to care for chronically ill older adults, there is less agreement on how to support healthier, low-income older adults to stay independent in their communities.

This study will compare the effectiveness of an in-home preventive healthcare program delivered by nurses to on-site health and wellness classes for older adults living in low-income independent housing. We also want to understand adherence and preferences of older adults for these two options.

Read more

The three-year study will take place in up to 18 low-income independent older adult apartment buildings in Los Angeles. Half of buildings will be randomized to offer the health and wellness classes, and the other half will offer the in-home preventive healthcare program. All study activities will be provided on-site at the building locations, and individuals living in the buildings will be invited to participate. A total of 480 participants will be recruited to participate, 240 in each group. Residents from participating buildings will meet with the research team to provide feedback throughout the study.

Other stakeholders, including doctors, housing services, social agencies, hospital leaders, professional societies, advocacy groups, and city policymakers will also meet with the team as an advisory group to share input and concerns. This project seeks to compare how each option maintains or improves health and functional independence in low-income older adults, with the goal of limiting dependency, moves to nursing homes, and the use of costly health services, while improving health behaviors and promoting the use of preventive health and appropriate community services.

Read the detailed description

EPIC is designed as a cluster randomized trial of low-income independent older adult housing locations in Los Angeles, CA. A total of 18 apartment buildings managed by five housing providers are currently available to be randomized. Buildings will be randomly selected two at a time, independent of housing provider. Prior to any research activity at each building, a social event will be scheduled to introduce the core research team to the building tenants and begin to further identify tenant opinion leaders. Subsequently, a mini health fair will be conducted in each building as part of research participant recruitment efforts. Baseline enrollment and assessment will be conducted prior to the building pair being randomly assigned, one to each study arm, to avoid bias in study enrollment. This design will allow us to study the effect of each strategy with an 18-month intervention, over a three-year study duration. The inclusion of apartment buildings - being the congregate focus of the interventions - are best suited to a cluster randomized controlled trial.

Core research team members, working closely with building staff and resident advisors, will tailor recruitment strategies - including pre-implementation social events, on-site receptions and health fairs, invitation letters and opportunities for residents to speak with the researchers. All tenants in each housing location will be invited to participate in our study of preventive health interventions and will agree at the minimum to be interviewed at baseline, the end of nine months, and the end of 18 months. The study will enroll as many as agree to participate (a minimum of 640 with up to 25% attrition to render a complete sample of 480 participants).

In keeping with the pragmatic nature of the community-based research and the circumstances of emerging from COVID pandemic, we will plan to complete a focused review and evaluation of the research implementation processes after the first two building pairs have been enrolled and two months of interventions have been provided to the four buildings.

Treatment Arms as Complex Interventions. In the past two decades, researchers addressing implementation of health promotion and prevention programs are acknowledging that these interventions are complex. Programs typically have multiple interacting components, address multiple risk factors, are implemented in multiple sites, and allow a certain amount of flexibility to adapt the intervention, tailoring to sites or groups. Variation in reported effectiveness is another feature of complex interventions, given that they reflect the different realities of varying health needs and responses within disparate populations and contexts. To maintain integrity complex interventions use guided processes, also called forms. Research studying complex interventions is meant to provide not only results about adherence and effectiveness, but commentary on what works best for whom, and how it works.

Given their interacting components and the multiple risk domains targeted by these interventions; both approaches being studied in this project, comprehensive health assessment and health and wellness classes, can be considered to be complex interventions. They are both premised upon the common function of disability prevention and address intra-individual factors as well as extra-individual factors that modify and slow or prevent the disablement process as described in the Verbrugge and Jette model. As complex interventions they are adapted to meet the individual needs of the participants and the context in which they are implemented.

Both interventions use forms (guided processes) that are standardized, but the ultimate intervention is a negotiation between participants and practitioners (nurses or educators). The guide for the APRN intervention is a standardized multi-dimensional health risk appraisal (based on CGA), risk identification, standardized recommendations negotiated with the participant and followed for reinforcement. The guide in the Classes intervention is a standardized curriculum with flexibility to modify according to participants' needs and preferences. The two intervention arms have different profiles of what risk factors for which they are stronger or weaker, and, critically, different patterns of adherence and attendance, i.e, the "self-administered" dose of any preventive actions being taken by the participants. The use of a Comparative Effective Research design enables a first-ever direct comparison of the outcomes associated with each complex intervention, and a wealth of data to explore how the interventions are received and evaluated by their users.

Conditions
Healthy Aging
Being tested
In-home Preventive Health Visits by Advanced Practice Nurse, On-site Evidence-based Physical Activity, Health and Wellness Classes
Keywords
Low Income Older Adults

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • In-home Preventive Health Visits by Advanced Practice NurseBehavioural

    Elements of Comprehensive Geriatric Assessment used as a preventive, health risk assessment, with recommendations tailored for health risks identified and offered to building tenants

  • On-site Evidence-based Physical Activity, Health and Wellness ClassesBehavioural

    Weekly calendar of health promotion and injury/illness prevention classes offered to building tenants.

Study groups in NCT05381480
Study groupRoleWhat they receive
In-home Preventive Health Visits by Advanced Practice NurseActive comparatorAPRNs will perform in-home multidimensional health assessment with quarterly follow up visits to provide individualized patient education, negotiation of recommendations to maintain/improve health and wellness. All participants continue to receive care from their primary care provider and other community-based providers, although use might be modified. Throughout the intervention, participants are encouraged to take a primary role in the management of their own health. APRNs coach and guide the participant in navigating existing service providers as well as accessing and establishing new services. Having the program in-home promotes an atmosphere of shared decision-making, while allowing the nurse to observe the physical and social environment. Key to this model is identification of individual profiles of health strengths and health risks; recommendations and negotiation over priority health behavior change; and quarterly follow up.
Receives: Behavioral: In-home Preventive Health Visits by Advanced Practice Nurse
On-site Evidence-based Physical Activity, Health and Wellness ClassesActive comparatorCurriculum. There will be three categories of classes offered at sites randomized into this intervention. A physical activity class will be offered three times weekly, and will include elements of Tai Chi, fall prevention, and arthritis exercises. Class content/activity will be modified for all levels of ability. A class focused on mental health and functioning will be offered weekly, and include activities targeting depression prevention, memory enhancement, and engagement (e.g., life review, agile mind). There will also be offered a weekly multi-topic class with a repeating cycle of topics and instructors including medication management, computer literacy and electronic health records, etc.. Tenants will be engaged in choosing topics that reflect the group consensus on importance. Altogether, at each location there will be five scheduled class opportunities each week for tenants to choose among.
Receives: Behavioral: On-site Evidence-based Physical Activity, Health and Wellness Classes

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. PROMIS 10-item Global Health Scale - Total Score

    Change in Total Score (standardized T-scores average = 50, SD = 10)

    Measured: Assessed at baseline, 9-months and 18-months (end of study)

  2. PROMIS 10-item Global Health Scale - Physical Functioning Subscale

    Change in Physical Functioning subscale (standardized T-scores average = 50, SD = 10)

    Measured: Assessed at baseline, 9-months and 18-months (end of study)

  3. PROMIS 10-item Global Health Scale - Mental Functioning Subscale

    Change in Mental Functioning subscale (standardized T-scores average = 50, SD = 10)

    Measured: Assessed at baseline, 9-months and 18-months (end of study)

Secondary outcomes (10)
  1. PROMIS Physical Functioning - Short Form 10b

    Change in average Physical Functioning score (1-5, 5 is highest functioning)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  2. PROMIS Self-Efficacy for Chronic conditions - Managing Daily Activities - Short Form 4a

    Change in average score (1-5, 5 is highest confidence)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  3. PROMIS short form for general self-efficacy - Short Form 4a

    Change in average score (1-5, 5 is highest confidence)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  4. PROMIS short form for self-efficacy for managing social interactions - Short Form 4a

    Change in average score (1-5, 5 is highest confidence)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  5. PROMIS Loneliness and Social Isolation (Ages 18+) fixed form

    Change in average score (1-5, 5 is most lonely/isolated)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  6. PROMIS Social Isolation - Short Form 4a

    Change in average score (1-5, 5 is most isolated)

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  7. Self Report of Number of Injury Falls in past 9 months

    Change in Number of Injury Falls and Likelihood of one or more Injury Falls

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  8. Health Services Use - Self Report of Number of ED Visits in past 9 months

    Change in Number of ED Visits and Likelihood of one or more ED Visits

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  9. Health Services Use - Self Report of Number of Hospital Admissions

    Change in Number of Hospital Admissions and Likelihood of one or more Hospital Admissions

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

  10. Health Services Use - Self Report of Number of SNF/Nursing Home/Rehab Admissions

    Change in Number of Admissions and Likelihood of one or more SNF/Nursing Home/Rehab Admissions

    Measured: Assessed at baseline enrollment, 9-months, 18 months (end of study)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 May 2022
  2. Study start22 Nov 2022
  3. Primary completion30 Sep 2024
  4. Study completion30 Sep 2024

Why it stopped: Funder requested change in contract which stopped enrollment at N = 104

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Cluster Randomized Controlled Trial, buildings randomized to one of two interventions
Masking
None (open label)
Enrolment
104 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05381480
Sponsor's protocol ID
STUDY00001884
Acronym
EPIC
Status last verified
Feb 2025
First submitted
21 Apr 2022
Last updated
14 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing In-home Preventive Health Visits by Advanced Practice Nurse and On-site Evidence-based Physical Activity, Health and Wellness Classes in people with Healthy Aging, run by Cedars-Sinai Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 14 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Funder requested change in contract which stopped enrollment at N = 104). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

PROMIS 10-item Global Health Scale - Total Score (time frame: Assessed at baseline, 9-months and 18-months (end of study)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Feb 2025.

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