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临床试验/NCT05481593
NCT05481593已完成不适用

An Accessible and Inclusive Artificial Intelligence Assisted Chronic Disease Self-Management Telehealth Platform: A Pilot Study

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 212 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
212
试验地点
2
主要终点
Health-related quality-of-life

研究概览

简要总结

The purpose of this study to pilot test an accessible and inclusive artificial intelligence (AI)-assisted, individualized, family-focused lifestyle modification intervention (AI4CHRON) for health-related quality of life for adults with impaired mobility and chronic medical conditions.

详细描述

The AI4CHRON study will use a four-arm randomized control trial design. Eligible and consented participants will be assigned to one of four groups: 1) Scheduled coaching calls with gamified rewards, 2) Scheduled coaching calls with rewards independent of gamification, 3) No scheduled coaching calls with gamified rewards, and 4) No scheduled coaching calls with rewards independent of gamification. The active intervention period will be six months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years or older
  • Diagnosis of heart disease, chronic lung disease, or Type 2 diabetes
  • Living with a permanent physical disability (i.e., spina bifida, multiple sclerosis, stroke,)
  • Have the ability to converse in and read English
  • Availability of a smartphone or computer

排除标准

  • Current enrollment in any structured intervention
  • Severe cognitive impairment
  • Severe untreated depression in the past 6 months
  • Major cardiac event in the past 12 months
  • Uncontrolled blood pressure
  • Resting tachycardia
  • Renal failure
  • Severe peripheral neuropathy
  • Active treatment for cancer in the past 12 months
  • Having both visual and hearing impairments (either of them is fine)

结局指标

主要结局

Health-related quality-of-life

时间窗: 24 Weeks

Enabled version of Short-Form 36 (SF-36E)

次要结局

  • Physical activity(24 weeks)
  • Self-efficacy for managing psychosocial illness(24 weeks)
  • Self-efficacy for managing medications(24 weeks)
  • Self-efficacy for managing social interactions(24 weeks)
  • Physical Activity(24 weeks)
  • Self-efficacy for managing sleep disturbance(24 weeks)
  • Self-efficacy for managing emotions(24 weeks)
  • Usability(24 weeks)
  • Self-efficacy for managing depression(24 weeks)
  • Dietary Intake(24 weeks)
  • Self-efficacy for managing daily activities(24 weeks)
  • Self-efficacy for managing sleep-related impairments(24 weeks)
  • Self-efficacy for managing symptoms(24 weeks)
  • Medication adherence(24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohanraj Thirumalai

Assistant Professor

University of Alabama at Birmingham

研究点 (2)

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