Actively Recruiting

Phase Not Applicable
Age: 30Years +
All Genders
NCT05920733

Healthy Lifetime - Phase 2

Led by University of Michigan · Updated on 2025-10-15

120

Participants Needed

1

Research Sites

169 weeks

Total Duration

On this page

Sponsors

U

University of Michigan

Lead Sponsor

M

Michigan Department of Health and Human Services

Collaborating Sponsor

AI-Summary

What this Trial Is About

HealthyLifetime (HL) is a person-centered program that enables older adults to maximize health and optimize functioning - the necessary requisite to successfully remaining independent in their preferred home setting as long as possible, i.e., to age in place.

CONDITIONS

Official Title

Healthy Lifetime - Phase 2

Who Can Participate

Age: 30Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be able to read, speak English and hear, using glasses or hearing aids if needed
  • Be able to provide their age, date of birth, address, phone number, and explain their health problems
  • Have their own computer or tablet with internet, a working camera, and microphone
  • Be able to use their device to join private video chat sessions like Zoom at home or in a private room
Not Eligible

You will not qualify if you...

  • Used the Emergency Room or stayed in the hospital in the last month
  • Not a verified user of Medicaid Home Help services
  • Have a new major health problem requiring doctor visits more than once per month
  • Been told their illness is not curable
  • Cannot remember their name, date of birth, or health problems
  • Cannot use glasses or hearing aids well enough to read materials or talk to the nurse
  • Do not have or cannot use a computer, tablet, or internet device at home for Zoom

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Michigan School of Nursing

Ann Arbor, Michigan, United States, 48109-5482

Actively Recruiting

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Research Team

M

Margaret Calarco, PhD

CONTACT

K

Kathleen Potempa, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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