Actively Recruiting

Phase Not Applicable
Age: 45Years +
MALE
Healthy Volunteers
NCT06276452

Supporting Resilience Among Re-entered Seniors

Led by University of Louisville · Updated on 2025-03-26

8

Participants Needed

1

Research Sites

142 weeks

Total Duration

On this page

Sponsors

U

University of Louisville

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The first goal (Aim 1) of this clinical trial is to learn about specific strengths, challenges, and desired areas of knowledge and skill-building among older adults who re-entered their communities from a period of incarceration and to then develop a new psychoeducational intervention tailored to these older adults. The second goal (Aim 2) of this clinical trial is to test if the intervention increases chronic disease management and whether the intervention is considered appropriate and acceptable by older adults who re-entered their communities from a period of incarceration. Aim 1 participants will: * complete a baseline survey * participate in a focus group Aim 2 participants will: * complete a baseline survey * participate in an 8-week once weekly intervention * complete three follow up surveys

CONDITIONS

Official Title

Supporting Resilience Among Re-entered Seniors

Who Can Participate

Age: 45Years +
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 45 years old
  • Have re-entered the community from a period of incarceration from jail or prison
  • Have at least one chronic health condition
  • Able to speak and understand English
Not Eligible

You will not qualify if you...

  • Aged 44 or younger
  • Have not re-entered the community from a period of incarceration from jail or prison
  • Do not have at least one chronic health condition
  • Unable to speak and understand English

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

New Legacy Reentry

Louisville, Kentucky, United States, 40203

Actively Recruiting

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Research Team

S

Stephanie Grace Prost, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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