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Идёт набор NCT07142499

Memory Support System for Older Chinese Americans With Mild Cognitive Impairment

Без фазы С лечением Mild Cognitive Impairment (MCI)

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: Memory Support System, Brain Health Education.
Кому может быть актуально
Состояния в реестре: Mild Cognitive Impairment (MCI). Базовые параметры: от 55 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

A Pilot of Memory Support System for Older Chinese Americans With Mild Cognitive Impairment

Обзор

The Memory Support System (MSS) from the Healthy Action to Benefit Independence \& Thinking® (HABIT) Program is an evidence-based, non-pharmacological intervention for mild cognitive impairment (MCI). Despite the clinical benefits and feasibility, the MSS was primarily developed and used with non-Hispanic White, English-speaking adults. Racial/ethnic minority groups are chronically under-enrolled in clinical trials for Alzheimer's Disease and Alzheimer's Disease Related Dementias (AD/ADRD) due to lack of linguistically and culturally appropriate adaptation of assessment measures and intervention protocols. The purpose of this research study is to examine whether the MSS from HABIT can help Chinese American older adults with mild thinking and memory problems. Target recruitment is 60 Chinese American adults who are primarily Mandarin- (n=30) and Cantonese-speaking (n=30). Forty participants will participate in the trainer-led day planner training and 20 will participate in self-study of the day planner and receive brain health education. Each participant will also be asked to identify a study partner to participate with them.

Вмешательства

  • Поведенческое Memory Support System
    Participants and study partners in the MSS treatment group will work with a study trainer to learn the MSS and eventually adapt the skills to support functioning in their daily life. The MSS trainer will follow a 10-session MSS Training Workbook as the standardized protocol for training. Additional sessions beyond the standard 10 sessions can be added if needed to support mastery of the MSS (up to a maximum of 15 total sessions). Participants and study partners will also receive a copy of the br
  • Поведенческое Brain Health Education
    Participants and study partners in the control group will be provided with the MSS guidebook and day planner for self-study of the MSS system. They will also meet with a study trainer to complete 10 sessions of a brain health education course that is tailored for individuals with MCI. The trainer will use a HABIT-based brain health education workbook to provide the content. Additional sessions beyond the standard 10 sessions can be added up to a maximum of 15 total sessions. Participants and stu

Первичные конечные точки

  • Recruitment rate [Срок оценки: baseline, week 1 of intervention session]
  • Retention rate [Срок оценки: baseline, treatment end (4-9 weeks)]
  • Completion rate [Срок оценки: baseline, treatment end (4-9 weeks)]
Вторичные конечные точки (11)
  • Everyday Cognition questionnaire [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Functional Activities Questionnaire (FAQ) [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • The Pillbox Test [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Dementia Rating Scale-2 (DRS-2) [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Chronic Disease Self-Efficacy Scales [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Quality of Life in Alzheimer Disease [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Neuropsychiatric Inventory Questionnaire (NPI-Q) - Severity [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Center for Epidemiologic Studies Depression Scale [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Anxiety Inventory Form [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Pittsburgh Sleep Quality Index [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]
  • Caregiver Burden Inventory Short-Form [Срок оценки: at baseline, treatment end (4-9 weeks), and 8-week follow-up]

Критерии участия

Критерии включения

  • self-identify as Chinese American;
  • age 55 and above;
  • a diagnosis of MCI as confirmed through documented clinical assessment and/or research-based diagnostic criteria;
  • predominantly Cantonese- or Mandarin-speaking;
  • able to read and write in Chinese;
  • visual and auditory acuity adequate for cognitive testing;
  • willing to complete the assessment measures;
  • having someone in regular contact to serve as a study partner/informant;
  • absence or stable use of prescribed memory-enhancing medications within the last 3 months.

Exclusion criteria include:

  • any significant neurologic disease that would impact their participation and completion of the trial;
  • history of psychiatry disorder (DSM 5 criteria) within the last 12 months;
  • history of reading or writing disability sufficient to interfere with MSS training; or
  • concurrent participation in another relevant clinical trial.

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
Лечение

Центры проведения

США · 1 центр
  • Li Lab, Icahn School of Medicine at Mount Sinai — New York

Идентификаторы

NCT: NCT07142499 · GCO 22-1738

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗