Меню
Идёт набор NCT07207993

Evaluating Health Outcomes of AI-Based Fitness Wearables and App Programs in Older Adults Living Alone With Cognitive Decline

Без фазы С лечением Older Adults With Cognitive Decline Older Adults AI-Based Fitness Wearables

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: Fitness app for self-efficacy, Social network via app for social support, Health education app targeting outcome expectations.
Кому может быть актуально
Состояния в реестре: Older Adults With Cognitive Decline, Older Adults, AI-Based Fitness, Wearables. Базовые параметры: от 65 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 →

Обзор

The overarching goal of our research is to develop personalized and accessible healthy aging lifestyle interventions aimed at promoting physical activity (PA) and improving health among community-dwelling older adults living alone with cognitive decline (LACD). To achieve this goal, the purpose of this project is to determine whether wearable and app-based mHealth intervention component(s) will contribute to increased PA and improved health outcomes in older adults LACD. Our specific aims are to: identify and evaluate mHealth intervention components that practically and significantly contribute to enhanced mechanistic outcomes (e.g., self-efficacy, outcome expectations) and increased PA (primary outcome) in older adults LACD over a 6-month period; determine the optimal combinations of intervention components for future efficacy testing; elucidate the mechanism of behavioral change (MoBC) and potential outcomes of these intervention components, namely, the mediating effects of MoBC variables (e.g., self-efficacy, outcome expectations) on the relationship between intervention components and change in PA. The first two aims are primary and fully-powered. The third aim is exploratory. The aims will support a refined, data-driven intervention design for a subsequent larger trial.

Подробное описание

Mobile health (mHealth) is a promising approach to improving health behaviors, defined as "health services and information delivered or enhanced through the Internet and related technologies." It includes disease prevention and management tools, remote interventions, personalized health monitoring, and mobile healthcare data access. With widespread technology adoption, researchers increasingly use wearable devices and apps to enhance health outcomes by promoting PA and reducing sedentary behavior. Wearable devices and fitness apps are now widely integrated into PA intervention programs, helping individuals adopt more active lifestyles. These tools track steps, activity duration, and progress, providing real-time feedback, goal-setting, and social integration to enhance motivation and behavior regulation. Notably, 21% of U.S. adults regularly use smartwatches or fitness trackers, making them feasible for PA interventions in older adults. RCTs have shown their positive effects on PA, QoL, and psychosocial well-being in older adults though some studies reported modest improvements. Recent advancements in data science and AI-driven mHealth interventions enable scalable, personalized exercise prescriptions. Personalized approaches, particularly those enhancing self-efficacy, yield better outcomes than generalized interventions. However, few studies have leveraged fitness wearables and apps for older adult LACD. This trial addresses this major weakness by implementing an AI-driven mHealth intervention for tailored precision health programs in older adult LACD.

Вмешательства

  • Другое Fitness app for self-efficacy
    AI-driven personalized exercise prescription via a fitness app. This targets self-efficacy.
  • Другое Social network via app for social support
    Participants will be provided access to a social network via app. This targets social support.
  • Другое Health education app targeting outcome expectations
    Participants are provided with an app-based health education. This targets outcome expectations.

Первичные конечные точки

  • Fitbit MVPA [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]
  • Physical Activity [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]
  • Mechanism of behavior change (MoBC) variables [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]
Вторичные конечные точки (3)
  • Quality of life (QoL) [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]
  • Psychosocial wellbeing [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]
  • Cognition [Срок оценки: Baseline (i.e., pre-intervention), 3 months (mid-point), and 6 months (end-point).]

Критерии участия

Критерии включения

  • Participant must be at least 65 years of age older
  • Participant must be living alone in the U.S. for the next 6 months
  • Participant must have report mild cognitive decline \[We will use a short self-report AD8 measure of cognitive concerns. Those scoring positive on the AD8 (≥2) will qualify as mild cognitive decline\];
  • Participant must own an Android/Apple smartphone
  • Participant must have access to internet or Wi-Fi access
  • Participant must be capable of engaging in some PA as determined by the PA Readiness Questionnaire or physician approval
  • Participant must currently participate in weekly moderate-to-vigorous PA (MVPA) or less than 150 minutes
  • Participant must have basic English communication skills.

Критерии исключения

  • Foreign residents or visitors

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Факторный дизайн
Маскирование
Двойное слепое
Основная цель
Профилактика

Центры проведения

США · 2 центра
  • University of Tennessee — Knoxville
  • The University of Tennessee, Knoxville. Health, Recreation, and Physical Education Buildin — Knoxville

Идентификаторы

NCT: NCT07207993 · STUDY00000016

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗