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Набор скоро начнётся NCT04871477

Adoption of Audio Recording in the Outpatient Supportive Care Center

Наблюдательное Advanced Malignant Solid Neoplasm Hematopoietic and Lymphoid Cell Neoplasm Locally Advanced Malignant Solid Neoplasm Metastatic Malignant Solid Neoplasm

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: Communication Intervention, Questionnaire Administration.
Кому может быть актуально
Состояния в реестре: Advanced Malignant Solid Neoplasm, Hematopoietic and Lymphoid Cell Neoplasm, Locally Advanced Malignant Solid Neoplasm, Metastatic Malignant Solid Neoplasm. 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

The Adoption of Audio Recording in the Outpatient Supportive Care Center

Обзор

This study evaluates how patients feel about having an audio recording of their visit to help remember information given to them and share that information with family members and/or caregivers not present during a clinic visit. Information from this study may help evaluate the effectiveness of using technology to help improve patient care by recording consultation recommendations.

Подробное описание

PRIMARY OBJECTIVE:

I. To assess the patient's perception of the usefulness of the audio recording in helping to recall information given to him/her in the visit along with the perception of usefulness in the dissemination of information to family member(s) and/or caregiver(s) not present at the clinic visit.

SECONDARY OBJECTIVES:

I. To assess the number of times the recording is listened to. II. To assess the ease of use of the technology. III. To assess the ability to share the information with the patient's family member(s) and/or caregiver(s) if he or she chooses to do so.

IV. To assess the patient perception of whether the audio recording caused any disruption to the clinic.

V. To estimate the participation rate of patients. VI. To explore association between patient's perception of the usefulness of the audio recording and patient's demographic/clinical characteristics.

VII. To explore the association between age and sex of the caregiver and frequency of caregiver's use of the audio recording.

VIII. To explore the association of the ease of use of the technology and the type of device and application used.

OUTLINE:

Patients audio record the recommendations and instructions given to them by the doctor record as part of their clinic visit at the Supportive Care Center.

Вмешательства

  • Другое Communication Intervention
    Audio record part of clinic visit
  • Другое Questionnaire Administration
    Ancillary studies

Первичные конечные точки

  • Proportion of patients who will select "Complete Agree/Partially Agree" in Question 1 "I found the audio recording useful after the visit" [Срок оценки: through study completion, an average of 1 year]
  • Proportion of patients who will select "Complete Agree/Partially Agree" in Question 2 "I was able to effectively discuss my medical condition with my family member(s) and/or caregiver(s) who were not present at the clinical visit [Срок оценки: through study completion, an average of 1 year]
Вторичные конечные точки (7)
  • Number of times the recording is listened to [Срок оценки: through study completion, an average of 1 year]
  • To assess the ease of use of the technology. [Срок оценки: through study completion, an average of 1 year]
  • To assess the ability to share the information with the patient's family member(s) and/or caregiver(s) if he or she chooses to do so. [Срок оценки: through study completion, an average of 1 year]
  • To assess the patient perception of whether the audio recording caused any disruption to the clinic [Срок оценки: through study completion, an average of 1 year]
  • Patient participation rate [Срок оценки: through study completion, an average of 1 year]
  • To explore the association between the frequency of caregivers' use of audio recording [Срок оценки: through study completion, an average of 1 year]
  • To explore the association of the ease of use of the technology and the type of device and application used [Срок оценки: through study completion, an average of 1 year]

Критерии участия

Критерии включения

  • Patients with the diagnosis of advanced cancer as defined as locally advanced, recurrent or metastatic cancer. Both solid and liquid tumors are eligible for the study
  • Patients who are seen in the outpatient supportive care center at M.D. Anderson Cancer Center
  • Patients who have access to a recording device or cellphone with recording technology
  • Patients who can be contacted 7 to 11 days from the clinic visit that the recording took place
  • Patients who can sign informed consent
  • Patients who are able to read and write in English
  • Patients 18 years or older

Критерии исключения

  • Patients who have been diagnosed with delirium or cognitive impairment. This will be defined by chart review along with review of the MD Anderson Symptom Inventory (MDAS) the day of clinic visit. An MDAS of 7 or greater will be considered to define delirium in this study
  • Patients who are unwilling to sign informed consent
  • Patients who have used audio recordings before in clinic visits
  • Patients who have severe hearing impairments without access to assisted devices or programs to aid in listening to the recorded material

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Только случаи

Центры проведения

США · 1 центр
  • M D Anderson Cancer Center — Houston

Идентификаторы

NCT: NCT04871477 · 2020-0240 · NCI-2021-02621 · 2020-0240

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗