Меню
Идёт набор NCT06794983

Calls and Coordination for Transitions of Care at Re-entry

Без фазы С лечением Prisoners Substance Use History Chronic Medical Conditions Psychiatric Condition

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: In-person visit with study team member, In-person visit with NCM, Phone calls and texts, Phone calls and texts - NCM.
Кому может быть актуально
Состояния в реестре: Prisoners, Substance Use History, Chronic Medical Conditions, Psychiatric Condition. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Health Systems Innovations for Supporting Transitions of Care for Incarcerated People Living With Substance Use Disorders

Обзор

The goal of this clinical trial is to learn if a short program for people being released from prison can help connect them to medical care. The main question it aims to answer is: * Will there be more non-emergency, outpatient clinic visits? Researchers will compare the number of clinic visits between people who use a Nurse Case Manager (NCM) to people in enhanced usual care. Participants will: * Complete surveys * Talk to a study team member 2-3 times, or talk to a study team member 2-3 times and talk to an NCM 6-11 times

Подробное описание

The objective of this clinical trial is to test the effectiveness of a transitional care program adapted to meet the healthcare needs of adults after release from prison. The goal of the transitional care intervention being tested is to help the study participants connect to primary care within 60 days of release through weekly check-in calls. Participants in this study are enrolled approximately 6 months before their anticipated release. One group will receive weekly phone calls for up to 60 days post-release. Additionally, novel, linked administrative datasets will be leveraged to enhance, contextualize, and clarify policy implications of the clinical trial results.

Вмешательства

  • Другое In-person visit with study team member
    Participants meet with a study team member before they are released from prison.
  • Другое In-person visit with NCM
    Participants meet with a NCM before they are released from prison.
  • Другое Phone calls and texts
    Study team member calls and texts participants after they are released from prison.
  • Другое Phone calls and texts - NCM
    Nurse case manager calls and texts participants after they are released from prison.

Первичные конечные точки

  • Number of participants who attend a Non-Emergency Outpatient Visit within 60 Days of Release From Prison [Срок оценки: 2 months post-release, approximately 5 months on study]
Вторичные конечные точки (1)
  • Number of participants who attend a Non-Emergency Outpatient Visit for Substance Use Disorder within 60 Days of Release From Prison [Срок оценки: 2 months post-release, approximately 5 months on study]

Критерии участия

Критерии включения

  • age 18 or older
  • eligibility for WI Medicaid and intention to enroll before release
  • substance use history (i.e., "have you ever considered your alcohol or drug use to be a problem?"), and
  • living with, or history of, a chronic medical or psychiatric condition other than substance use disorder. This is defined as ever having been diagnosed with a medical or psychiatric chronic condition, or currently taking prescription medications for a chronic condition.
  • able to read, understand, and speak English.

Критерии исключения

  • ineligible for WI Medicaid
  • no substance use history
  • not living with, or no history of, chronic medical or psychiatric condition

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

США · 1 центр
  • University of Wisconsin — Madison

Идентификаторы

NCT: NCT06794983 · 2024-1669 · 2R01DA047889-06 · A538500 · Protocol Version 11/8/2024 · SMPH/POP HEALTH SCI/POP HLTH

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗