跳至主要内容
临床试验/NCT06276452
NCT06276452招募中不适用

Supporting Resilience Among Re-entered Seniors

University of Louisville2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2024年3月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
8
试验地点
2
主要终点
Chronic disease self managment

研究概览

简要总结

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

详细描述

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

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Supporting resilience psychoeducational group

Experimental

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.

干预措施: Psychoeducation (Behavioral)

结局指标

主要结局

Chronic disease self managment

时间窗: 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)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stephanie Prost

Associate Professor

University of Louisville

研究点 (2)

Loading locations...

相似试验