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DiaBuddy: AI-Enabled Digital Self-Management for Youth With Type 1 Diabetes (DiaBuddy)

2026年10月3日 更新者:Dr. Juwayria Omar

Effect of an AI-Empowered Digital Self-Management Intervention on Glycemic Control and Caregiver Burden in Children and Adolescents With Type 1 Diabetes Mellitus: A Multicenter Randomized Controlled Trial in Pakistan

The goal of this clinical trial is to learn whether DiaBuddy, a digital self-management app, can help children and adolescents with Type 1 diabetes better manage their condition and reduce the burden experienced by their caregivers. The study will include children and adolescents aged 6 to 17 years with Type 1 diabetes who live in Pakistan.

The main questions it aims to answer are:

  • Does using DiaBuddy along with usual diabetes care improve diabetes self-management and adherence?
  • Does using DiaBuddy along with usual diabetes care reduce caregiver burden?
  • Does using DiaBuddy affect blood sugar control, diabetes-related distress, and other diabetes-related health outcomes?
  • Is DiaBuddy acceptable and useful for children, adolescents, and their caregivers?

Researchers will compare participants who use DiaBuddy along with their usual diabetes care with participants who receive usual diabetes care alone.

Participants will:

  • Use DiaBuddy to record and review information related to their diabetes, including blood glucose and self-management activities.
  • Receive diabetes education, reminders, and self-management support through the app.
  • Complete questionnaires about diabetes self-management, diabetes-related experiences, and caregiver burden.
  • Have blood sugar control assessed through laboratory-verified HbA1c measurements.
  • Attend scheduled follow-up assessments at approximately 3 and 6 months.
  • Report relevant diabetes-related health events, such as hypoglycemia, diabetic ketoacidosis, emergency visits, and hospitalization.

研究概览

详细说明

Type 1 diabetes mellitus (T1DM) requires continuous daily management, including glucose monitoring, insulin administration, dietary decisions, physical activity, recognition of abnormal glucose levels, and management of diabetes-related risks. For children and adolescents, this management is shared between the child and caregiver, and responsibility gradually shifts toward the child with increasing age and independence. This can create challenges related to adherence, diabetes-related distress, and caregiver burden.

DiaBuddy is an artificial intelligence (AI)-empowered digital self-management intervention developed to support children and adolescents with T1DM and their caregivers. The intervention is intended to complement, rather than replace, routine diabetes care. It provides digital tools for recording and reviewing diabetes-management information, educational content, reminders, motivational features, and caregiver support.

The application includes functions such as glucose logging and trend visualization, insulin and meal/snack reminders, physical activity reminders, hypoglycemia alerts, diabetes safety and diabetic ketoacidosis (DKA) education, educational videos, interactive quizzes, Urdu and English content, points, badges and rewards, caregiver dashboards, child-caregiver account linking, weekly summaries, synchronization, offline functionality where supported, and technical support.

DiaBuddy will also incorporate AI-supported analysis of available longitudinal diabetes-management information, such as glucose readings, insulin information, dietary information, physical activity information, and previous glucose patterns. The AI may provide individualized information concerning glucose trends, dietary considerations, physical activity, anticipated glucose patterns, diabetes-management reminders, and when medical review may be appropriate.

The AI component is designed as a decision-support and self-management tool. It will not independently change or administer insulin doses. Any insulin-related suggestion will remain subject to the participant's or caregiver's existing clinical management plan and treating clinician oversight. DiaBuddy will not replace treating physicians, routine diabetes care, emergency medical services, or clinical decision-making.

The definitive trial follows a preliminary DiaBuddy pilot. The pilot provided information about feasibility, usability, technical issues, questionnaire administration, recruitment, follow-up, and preliminary changes in self-management, caregiver burden, diabetes-related distress, and reported caregiving time. Because the pilot did not include a control group and was short in duration, it cannot determine whether observed changes were specifically attributable to DiaBuddy. The randomized controlled trial is therefore designed to provide a controlled comparison of DiaBuddy added to usual diabetes care versus usual diabetes care alone.

Participants will be followed for six months, with assessments planned at baseline, approximately three months, and approximately six months. Clinical and participant-reported information will be collected throughout follow-up. Laboratory-verified glycated hemoglobin (HbA1c) will be used to assess glycemic control. The study will also monitor relevant diabetes-related events and healthcare utilization, including hypoglycemia, severe hypoglycemia, DKA, emergency department visits, and diabetes-related hospitalization.

Safety monitoring will include potentially harmful AI outputs and technical failures that could affect participant safety in addition to clinical safety events. Participants will be informed that DiaBuddy is not an emergency service and that clinical emergencies should be managed through their treating healthcare team or appropriate emergency services.

Before the trial begins, the randomized controlled trial (RCT) version of the application will be documented, including the permitted and prohibited AI outputs, insulin-related safeguards, human oversight procedures, software and AI version control, handling of erroneous or incomplete information, and procedures for reporting potentially serious AI-related incidents. Changes to the software or AI system during the trial will be documented.

The trial is intended to determine whether adding DiaBuddy to usual diabetes care provides meaningful improvements in diabetes self-management and caregiver outcomes while also evaluating clinical outcomes, safety, usability, and engagement. The longer-term objective is to develop a safe and evidence-based digital self-management platform that may subsequently be evaluated for implementation within routine diabetes care in Pakistan.

研究类型

介入性

注册 (估计的)

140

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

6年 至 17年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Children and adolescents aged 6-17 years at the time of enrollment.
  2. Confirmed diagnosis of Type 1 diabetes mellitus for at least 6 months.
  3. Resident of Pakistan.
  4. Parent or primary caregiver actively involved in the participant's diabetes care and willing to participate in the study.
  5. Access to a compatible smartphone or digital device capable of running the DiaBuddy application.
  6. Parent or legally authorized representative willing to provide informed consent.
  7. Child/adolescent willing to provide age-appropriate assent, where applicable.
  8. Participant and caregiver willing and able to comply with study procedures and follow-up assessments.

Exclusion Criteria:

  1. Cognitive, developmental, or other impairment that substantially limits the participant's ability to understand or use the intervention or complete study assessments.
  2. Severe or unstable medical illness that, in the judgment of the study investigator, would substantially interfere with study participation or follow-up.
  3. End-stage renal disease.
  4. Proliferative diabetic retinopathy.
  5. Recurrent severe diabetic ketoacidosis requiring intensive care that would substantially interfere with study participation or follow-up.
  6. Any other medical, psychosocial, or logistical condition that, in the judgment of the investigator, would make participation inappropriate or prevent completion of the study procedures.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:DiaBuddy + Usual Diabetes Care

Participants assigned to this arm will receive access to DiaBuddy in addition to their usual diabetes care for 6 months. DiaBuddy is an AI-empowered digital self-management and decision-support intervention that provides tools for glucose logging and trend visualization, insulin, meal/snack, and physical activity reminders, hypoglycemia alerts, diabetes safety and DKA education, educational videos and quizzes, Urdu and English content, motivational features, caregiver support, and weekly summaries. The AI component may provide individualized self-management information and recommendations based on available diabetes-management information. DiaBuddy will not independently change or administer insulin doses and will not replace routine clinical care or emergency medical services.

DiaBuddy is an AI-enabled digital self-management intervention designed to support children aged 6-17 years with T1DM and their caregivers. The intervention provides tools for glucose logging and trend visualization, insulin and medication reminders, snack and exercise reminders, hypoglycemia and DKA educational alerts, diabetes education through videos, quizzes, cartoons and animations, and English and Urdu language options. It also includes points, badges and rewards to encourage engagement, caregiver-child linking, and a caregiver dashboard with weekly summaries. AI-supported features may assist with interpretation of glucose trends and provide general self-management recommendations; however, the system does not autonomously modify insulin doses, and insulin-related decisions remain under clinical supervision. Participants will use DiaBuddy alongside their usual diabetes care during the intervention period.

有源比较器:Usual Care

Participants in this arm will receive usual standard diabetes care as provided by their treating healthcare team. They will not receive access to the DiaBuddy digital intervention during the study period. Usual care may include routine clinical follow-up, insulin therapy, blood glucose monitoring, dietary and physical-activity guidance, diabetes education, and other standard services according to the participant's treating team.

Participants assigned to the usual care arm will continue to receive standard diabetes care according to the routine practices of their treating healthcare team. Usual care may include routine clinical follow-up, insulin therapy, blood glucose monitoring, dietary and physical-activity counseling, diabetes education, and management of acute and chronic diabetes-related concerns as clinically indicated. Participants in this arm will not receive access to the DiaBuddy digital self-management intervention during the study period.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Child Diabetes Self-Management/Adherence Score
大体时间:Baseline and 6 months after randomization

Change in child diabetes self-management/adherence score assessed using the modified Self-Care Inventory-Revised (SCI-R). Higher scores indicate better self-management/adherence.

Baseline and 6 months after randomization

次要结果测量

结果测量
措施说明
大体时间
Change in Child Diabetes-Related Distress Score
大体时间:Baseline and 6 months after randomization

Change in diabetes-related distress assessed using the study's specified child distress measure/emoji-based assessment. Lower scores indicate lower diabetes-related distress.

Baseline and 6 months after randomization
Change in Glycated Hemoglobin (HbA1c) Level
大体时间:Baseline and 6 months after randomization

Change in glycated hemoglobin (HbA1c), measured as a clinical indicator of glycemic control.

Baseline and 6 months after randomization
Change in Diabetes-Related Caregiving Time
大体时间:Baseline and 6 months after randomization

Change in caregiver-reported time spent on diabetes-related caregiving activities, reported in hours per day. Lower values indicate reduced caregiving time.

Baseline and 6 months after randomization

其他结果措施

结果测量
措施说明
大体时间
Number of Participants With Diabetes-Related Adverse Events
大体时间:Throughout the 6-month intervention period

Occurrence of hypoglycemia, severe hypoglycemia, diabetic ketoacidosis (DKA), emergency department visits, and diabetes-related hospitalizations will be recorded and compared between study arms.

Throughout the 6-month intervention period

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月2日

初级完成 (估计的)

2027年6月2日

研究完成 (估计的)

2027年9月2日

研究注册日期

首次提交

2026年9月28日

首先提交符合 QC 标准的

2026年10月3日

首次发布 (实际的)

2026年10月6日

研究记录更新

最后更新发布 (实际的)

2026年10月6日

上次提交的符合 QC 标准的更新

2026年10月3日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Individual participant data underlying the results reported in the publication, after de-identification, may be shared with qualified researchers upon reasonable request. Data that could directly or indirectly identify participants will not be shared. Requests will be reviewed by the study investigators and will be subject to applicable ethical, privacy, and data-protection requirements. The shared dataset may include de-identified participant characteristics, intervention assignment, outcome measures, and relevant baseline and follow-up data. Data will be made available after publication of the primary study results, subject to appropriate data-use requirements.

IPD 共享时间框架

IPD will be available beginning 12 months after publication of the primary study results and will remain available for 5 years. Supporting information will be available during the same period.

IPD 共享访问标准

Access will be available to qualified researchers who submit a reasonable request for scientifically valid research purposes. Requests will be reviewed by the study investigators and must comply with applicable ethical, privacy, and data-protection requirements. Approved researchers will receive access to relevant de-identified individual participant data and selected supporting documents through a secure data-sharing process. Data will not be provided in a form that permits participant identification.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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