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临床试验/NCT05535842
NCT05535842招募中不适用

Conversational Agent for Supporting People With Type 2 Diabetes and Their Carers

Nanyang Technological University4 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2022年11月28日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
224
试验地点
4
主要终点
Changes in diabetes knowledge among patients and carers using Diabetes Knowledge Questionnaire at baseline, interim (3 months) and end-of-trial (6 months).

研究概览

简要总结

Diabetes self-management support, education, and training are increasingly being delivered through digital technology such as mobile phones. This protocol aims to evaluate the effectiveness of GLOW, a diabetes companion app with a conversational agent.

详细描述

Adopting a healthier lifestyle and disease self-management skills is critical to reducing the risk of diabetes-related complications. Internationally, and in Singapore, the majority of people with diabetes report not having received structured diabetes education, while others have the knowledge and fail to apply it in their daily lives.

Key self-management behaviours recommended by the American Association of Diabetes Educators include physical activity, healthy diet, blood glucose monitoring, and medication adherence, but equally important is healthy coping to maintain a positive attitude toward diabetes management. Life-long patient education and continuous empowerment are paramount to successful self-management in people with diabetes, as recommended by evidence-based diabetes management guidelines.

In addition to patients, their informal carers often play an important role in the management of diabetes. As such, diabetes education for informal carers is essential to achieve the best possible diabetes outcomes in the patient.

There are hundreds of diabetes apps available for the public to download and use, but few are rigorously evaluated for clinically meaningful outcomes. We designed GLOW, a diabetes companion app with a conversational agent, to support people with diabetes and their carers with self-management and knowledge.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

盲法说明

non-blinded

入排标准

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

入选标准

  • Diagnosed with type 2 diabetes and attending Tan Tock Seng Hospital (TTSH) Diabetes Clinic OR caring for a person with type 2 diabetes
  • 21 years old or above
  • Able to speak and read English
  • Singapore nationality or permanent resident or foreign domestic worker (for carers)
  • Own a personal mobile device which can download study mobile app
  • Access to the internet

排除标准

  • Are unable to consent;
  • Are pregnant (for patients)
  • Received formal training in medicine or allied health services

结局指标

主要结局

Changes in diabetes knowledge among patients and carers using Diabetes Knowledge Questionnaire at baseline, interim (3 months) and end-of-trial (6 months).

时间窗: baseline, interim (3 months), end-of-trial (6 months)

The changes in diabetes knowledge will be measured using the scores of a validated questionnaire, Diabetes Knowledge Questionnaire (DKQ).

Changes in diabetes knowledge among patients and carers in the intervention group using GLOW Quiz at baseline, interim (3 months) and end-of-trial (6 months).

时间窗: baseline, interim (3 months), end-of-trial (6 months)

The changes in diabetes knowledge among patients and carers in the intervention group will be measured using the scores of a new quiz developed based on GLOW modules, GLOW Quiz.

次要结局

  • Changes in BMI among patients at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in waist circumference among patients at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in glycemic controls measured by HbA1c among patients at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in fasting blood glucose levels among patients at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in systolic and diastolic blood pressure among patients at baseline, interim (3 months), end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in serum high density lipoprotein (HDL) levels among patients at baseline, interim (3 months), end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in serum low density lipoprotein (LDL) levels among patients at baseline, interim (3 months), end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in total cholesterol levels among patients at baseline, interim (3 months), end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in number of diabetes related hospitalization among patient at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in medical cost of diabetes related hospitalization among patient at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in patients empowerment levels score using, Diabetes Empowerment Scale, at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in patients attitude and behaviour score using Diabetes Intention, Attitude, and Behaviour Questionnaire (DIAB-Q), at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • GLOW App login period among patients and carers in the intervention group will be measured at the end-of-trial (6 months).(end-of-trial (6 months))
  • GLOW App module completion among patients and carers in the intervention group will be measured at the end-of-trial (6 months).(end-of-trial (6 months))
  • GLOW App usability perception among patients and carers in the intervention group will be measured at the end-of-trial (6 months).(end-of-trial (6 months))
  • Changes in patients and carers quality of life will be measured using EQ-5D-5L Questionnaire, at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in caregiving levels among carers using Diabetes Caregiver Activity and Support Scale at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • Changes in caregiving burden among carers using Brief Assessment Scale for Caregivers at baseline, interim (3 months) and end-of-trial (6 months).(baseline, interim (3 months), end-of-trial (6 months))
  • GLOW App login frequency among patients and carers in the intervention group at will be measured the end-of-trial (6 months).(end-of-trial (6 months))

研究者

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

Josip Car

Director, Center for Population Health Sciences, Lee Kong Chian School of Medicine

Nanyang Technological University

研究点 (4)

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