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Supporting Resilience Among Re-entered Seniors (SRRS)

University of Louisville (UOFL) logo

University of Louisville (UOFL)

Status

Enrolling

Conditions

Chronic Disease

Treatments

Behavioral: Psychoeducation

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06276452
U2CDA050097 (U.S. NIH Grant/Contract)
23.0434

Details and patient eligibility

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

Full description

The protocol for Aim 2 will be developed once the focus group data is analyzed.

Enrollment

8 estimated patients

Sex

Male

Ages

45+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

8 participants in 1 patient group

Supporting resilience psychoeducational group
Experimental group
Description:
This group-based psychoeducational intervention will take place once weekly for eight weeks and will be centered upon building older adults' knowledge, skills, and motivation to manage chronic disease.
Treatment:
Behavioral: Psychoeducation

Trial contacts and locations

1

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Central trial contact

Stephanie Grace Prost, PhD

Data sourced from clinicaltrials.gov

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