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临床试验/NCT07458997
NCT07458997尚未招募不适用

Usability Evaluation of Gen AI-based Nutrition Chatbot for Pregnant Women: A Pilot Quasi-experimental Study

Hong Kong Metropolitan University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
System Usability Scale (SUS)

研究概览

简要总结

Background: Pregnancy imposes significant physical demands, with complications like gestational diabetes (GDM) and pre-eclampsia posing serious risks. Nutrition is crucial for mitigation, but accessing reliable guidance remains challenging. This study evaluates the feasibility of an AI chatbot providing nutritional guidance for managing these conditions.

Methods: In a quasi-experimental design, 100 pregnant women will self-select into either the intervention group (n=50, using an AI chatbot) or control group (n=50, receiving standard care). The primary outcome is usability measured by the System Usability Scale (SUS) at 12 weeks, with an expected mean difference of ≥13 points. Secondary outcomes include technology acceptance (Technology Acceptance Model), user engagement, information accuracy, and changes in dietary knowledge/behaviors. Quantitative data will be analyzed using intention-to-treat and t-tests. Semi-structured interviews with 20 participants will explore user experiences through thematic analysis.

Expected Results: The AI chatbot is anticipated to demonstrate superior usability and high user acceptance (TAM >5.0/7), with improvements in dietary knowledge and behavior. Qualitative findings will provide insights into benefits, barriers, and engagement factors.

Conclusion: This study will establish an evidence base on AI chatbot feasibility and acceptance for prenatal nutrition, informing tool optimization and future large-scale trials.

详细描述

Objectives: This study primarily aims to evaluate the usability of a nutrition AI chatbot for pregnant women by comparing System Usability Scale (SUS) scores between intervention and control groups. Secondary objectives include assessing technology acceptance (Technology Acceptance Model), engagement patterns, information quality (accuracy, comprehensibility, consistency), and changes in nutritional knowledge.

Design: A quasi-experimental design with two parallel groups (n=50 each) will be employed. Using self-selection, participants will choose to enroll in the intervention group (access to an AI chatbot plus routine care) or the control group (access to a standardized WeChat information service plus routine care). Routine care for all participants includes standard prenatal clinic visits and printed nutritional materials.

The WeChat service for the control group will be operated by a trained research assistant using a pre-defined script during two scheduled windows daily, providing information quoted from the official nutritional leaflets. This isolates the mode of information delivery (AI versus human-facilitated messaging) as the primary variable.

Participants: Inclusion criteria: pregnant women aged ≥18 years, able to consent, owning a smartphone with internet access. Exclusion criteria: enrollment in other nutrition interventions or severe mental health conditions impairing technology use. A purposive subsample of 20 participants (10 per group) will complete qualitative interviews.

Sample Size: Based on an expected mean SUS score of 78 (SD=12) in the intervention group and 65 (SD=15) in the control group (Cohen's d=0.95), 23 participants per group are required for 90% power at alpha=0.05. Accounting for 50% attrition, 50 participants per group will be recruited. Propensity score matching will be applied to reduce selection bias using variables including age, gestational age, parity, education, and baseline technology use.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Pregnant women aged 18 years or older
  • Able to provide informed consent in the study language
  • Own a smartphone with internet access and the WeChat application

排除标准

  • Current enrollment in other nutrition intervention studies
  • Severe mental health conditions that may impair technology use or ability to provide informed consent

研究组 & 干预措施

The intervention group

Experimental

The intervention group will access the the nutrition AI chatbot.

干预措施: a culturally tailored nutrition AI chatbot for pregnant women (Behavioral)

The control group

No Intervention

The control group will receive routine care along with access to a standardized WeChat information service. To ensure a fair comparison, the WeChat service for the control group will be operated by a trained research assistant using a pre-defined script and protocol. The assistant will respond to enquiries during two pre-scheduled windows per day (e.g., 10:00-12:00 and 14:00-16:00) by providing information directly quoted or paraphrased from the official nutritional leaflets.

结局指标

主要结局

System Usability Scale (SUS)

时间窗: 12weeks

Usability will be assessed using the System Usability Scale (SUS), a 10-item questionnaire with five-point Likert responses. SUS yields a total score ranging from 0 to 100, with higher scores indicating better perceived usability. Scores will be compared between groups at 12 weeks.

次要结局

  • Mean Score on the Technology Acceptance Model (TAM) Questionnaire(12 weeks)
  • Proportion of Participants Achieving Adequate Engagement Adherence(12 weeks)
  • Mean Number of Platform Logins per Week(12 weeks)
  • Mean Number of Queries Submitted per Participant(12 weeks)
  • Proportion of Chatbot Responses Rated as Accurate by Clinical Expert Panel(12 weeks)

研究者

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

Dr Bronya LUK Hi Kwan

Assistant Professor

Hong Kong Metropolitan University

研究点 (1)

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