NCT07361601

Brief Summary

This study will longitudinally follow a cohort of older adults to better understand how decisions about aging in place or transitioning to long-term care-and the implementation of those decisions-are influenced by age-related changes (e.g., cognition, health literacy, chronic conditions) and social supports (e.g., caregivers).

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
285

participants targeted

Target at P75+ for all trials

Timeline
69mo left

Started Apr 2026

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress2%
Apr 2026Dec 2031

First Submitted

Initial submission to the registry

January 21, 2026

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 23, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2030

Expected
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2031

Last Updated

January 23, 2026

Status Verified

January 1, 2026

Enrollment Period

4 years

First QC Date

January 21, 2026

Last Update Submit

January 21, 2026

Conditions

Keywords

Aging in placeLong term care planning

Outcome Measures

Primary Outcomes (1)

  • Rate of participant long term care planning for Alzheimer's Dementia/Memory Loss

    Participants are asked "If you developed Alzheimer's or memory loss and could no longer live independently in your home, have you decided what your living preferences (e.g. stay in own home, retirement/long term care community) would be?" Decision-making is measured as a binary ('yes', 'no') outcome at each time-point. Will report % of participants who indicated "YES", that they have decided on their living preferences. Frequencies given for 108 month timepoint per primary outcome analysis.

    Assessed every 6 months, 108 months reported

Secondary Outcomes (9)

  • Rate of participant planning for in-home care in the event of Alzheimer's Disease/Memory Loss

    Assessed every 6 months, 108 months reported

  • Rate of participant planning for memory care in the event of Alzheimer's Disease/Memory Loss

    Assessed every 6 months, 108 months reported

  • Rate of participant planning for a hospitalization requiring rehabilitation outside the home

    Assessed every 6 months, 108 months reported

  • Rate of participant planning for a hospitalization requiring in-home care

    Assessed every 6 months, 108 months reported

  • Rate of participant decision-making contemplation: Alzheimer's Dementia/Memory Loss (ADML)

    Assessed every 6 months, 108 months reported

  • +4 more secondary outcomes

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of a cohort of older adults who are currently enrolled in the longitudinal study, R01AG058777. Older adults as well as their caregivers, where appropriate, are being followed over time to assess decision-making and planning related to aging in place and potential transitions to long-term care. The cohort includes individuals with varying levels of cognitive function, health status, chronic conditions, and social support, as well as diverse living environments (e.g., rural and urban settings, different types of housing). Participants will continue to be followed prospectively.

You may qualify if:

  • Active participant in the 'Decision Making and Implementation of Aging-in-Place/Long Term Care Plans among Older Adults' \[R01AG058777\] study;
  • Age 65 years or older (older adult); age 18 years or older (caregiver)
  • Speak English; and
  • Pass UBACC (University of California, San Diego Brief Assessment of Capacity to Consent) cognitive assessment
  • Age 18 years or older;
  • Speak English;
  • Currently assist enrolled, older adult study participant with activities such as managing their health, and/or household activities (i.e., taking them to the doctor, housekeeping, meal prep, medication reminders); and
  • Pass UBACC (University of California, San Diego Brief Assessment of Capacity to Consent) cognitive assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northwestern University

Chicago, Illinois, 60611, United States

Location

MeSH Terms

Conditions

Alzheimer DiseaseCognitive Dysfunction

Condition Hierarchy (Ancestors)

DementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental DisordersCognition Disorders

Study Officials

  • Lee A Lindquist, MD MPH MBA

    Northwestern University Feinberg School of Medicine

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Vanessa Ramirez-Zohfeld, MPH

CONTACT

Charlie Olvera, MA, MS

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Medicine, Section Chief - Geriatrics

Study Record Dates

First Submitted

January 21, 2026

First Posted

January 23, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

March 31, 2030

Study Completion (Estimated)

December 31, 2031

Last Updated

January 23, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

There is no plan to make IPD and related data dictionaries available.

Locations