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Набор по приглашению NCT07192419

Promoting Aging and Thriving With HIV

Без фазы С лечением HIV (Human Immunodeficiency Virus) Geriatric Geriatric Assessment HIV

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: Promoting Aging and Thriving with HIV (PATH)-Implementation of a Tailored Geriatric Assessment and Management Strategy for HIV Care Settings.
Кому может быть актуально
Состояния в реестре: HIV (Human Immunodeficiency Virus), Geriatric, Geriatric Assessment, HIV. Базовые параметры: от 50 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
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Официальное название

Promoting Aging and Thriving With HIV (PATH)-Implementation of a Tailored Geriatric Assessment and Management Strategy for HIV Care Settings

Обзор

The pilot is an intervention of a geriatric assessment and management tool (PATH) in outpatient HIV clinics.

Подробное описание

This will be a Pilot, two-arm, randomized parallel-group, clinical trial with blinded research staff of a Geriatric assessment and management tool vs usual care to evaluate the feasibility, acceptability, and preliminary efficacy of the tool on quality of life for older adults with HIV.

Вмешательства

  • Поведенческое Promoting Aging and Thriving with HIV (PATH)-Implementation of a Tailored Geriatric Assessment and Management Strategy for HIV Care Settings
    For the intervention arm, participants will be sent geriatric assessment questions through the patient portal in advance of a routine HIV appointment. If the participant is unable to complete the questions in advance, they will be done with the help of a research coordinator to go through on the day of appointment. Every attempt will be made to ensure the assessment can be done in advance of the appointment, however the study team will allow for visits after the regular appointment as in which c

Первичные конечные точки

  • Feasibility: recruitment and retention [Срок оценки: Recruitment day one, throughout the study to final assessment six months post baseline of the last participant.]
  • Feasibility: patient/provider experience [Срок оценки: After completing final outcomes at the 6 month assessment (or earlier if difficulty with recruitment/retention) patients and providers will be invited to participate in an optional qualitative interview.]
  • Acceptability; General attitudes, perception of intervention [Срок оценки: After completing final outcomes at the 6 month assessment (or as needed if difficulty with recruitment/retention) patients and providers will be invited to participate in an optional qualitative interview.]
Вторичные конечные точки (3)
  • Impact of PATH Outcomes: measured by identification of geriatric conditions [Срок оценки: Geriatric Conditions will be measured through chart review at baseline, 3month, and 6 month assessments to determine overall change from baseline.]
  • Impact of PATH Outcomes: measured by addressing unmet needs. [Срок оценки: Unmet needs will be measured through survey questions and chart review at baseline, 3month, and 6 month assessments.]
  • Quality of life as measured by Medical Outcomes 36-Item Short Form Survey (SF-36) [Срок оценки: Quality of life will be measures at baseline, 3 months and 6 months post baseline assessments.]

Критерии участия

Критерии включения

  • Age 50 or older
  • Receive HIV care (at least 1 visit at the same site within the past 12 months) from either Eskenazi Health IDC or LifeCare clinics,
  • Able to provide informed consent

Критерии исключения

  • Patients who are long-term nursing home residents
  • Patients who are receiving geriatric care services, however will liberalize this criteria if difficulty with recruitment

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
Простое слепое
Основная цель
Скрининг

Центры проведения

США · 2 центра
  • Eskenazi Health — Indianapolis
  • IU Health LifeCare — Indianapolis

Идентификаторы

NCT: NCT07192419 · 27767 · K76AG064545-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗