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NCT Number: NCT06276452

Supporting Resilience Among Re-entered Seniors

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

Recruiting

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Key information

Conditions

Chronic Disease Disease Attributes Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

45 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

New Legacy Reentry

Louisville, Kentucky, 40203, United States

Location status: Recruiting

Location contact

Stephanie Grace Prost, PhD

CONTACT

[email protected]

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Psychoeducation

Behavioral

Psychoeducation is the therapeutic management of illness through the increase of related knowledge, skills, and motivation.

Primary outcomes

  1. Chronic disease self managment

    Time frame: 12 weeks

    Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Chronic Conditions measures (viz. daily activities, medications and treatments, symptoms, emotions, social interactions)

Study contacts

Contact information is provided by the study sponsor or research team.

Stephanie Grace Prost, PhD

CONTACT

[email protected]

850-491-0285

Sponsors and collaborators

Lead sponsor

University of Louisville

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Acronym: SRRS

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 26, 2024
Registry last updated
Mar 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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