Exploring the Effectiveness of AI Generative Models for Diabetic Patients

Sponsor
Pakistan Council of Scientific and Industrial Research (Other)
Overall Status
Recruiting
CT.gov ID
NCT05883072
Collaborator
(none)
300
1
47.8
6.3

Study Details

Study Description

Brief Summary

We plan to explore the usability of Generative AI-Chatbot for Diabetic Patient

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exploring AI-Chatbot

Detailed Description

Diabetes is rapidly spreading, affecting a significant number of adults, with a staggering total of 537 million diabetic individuals. This condition gives rise to various complications that can lead to diabetic retinopathy, foot ulcers, cardiac problems, and kidney damage. However, many of these complications can be mitigated by providing patients with accurate information concerning their diet, stress management, and weight control.

The recent advancements in Generative Artificial Intelligence-based chatbots have demonstrated their efficacy as intelligent assistants across various aspects of human life. In this study, we aim to assess the effectiveness of these Language Models in assisting patients. Our research plan entails the interaction between patients and chatbots like ChatGPT, both with and without human support, followed by evaluations of these interactions by specialists. Additionally, we will gather feedback from patients regarding their experiences and perceptions of the chatbot interactions.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Exploring the Effectiveness of AI Generative Models for Diabetic Patients
Actual Study Start Date :
Jan 5, 2023
Anticipated Primary Completion Date :
Dec 30, 2024
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Intervention

Patients will be provided access to Chatbot to enquire their querries regarding diabetic complications.

Behavioral: Exploring AI-Chatbot
All participants will be provided access to AI-Chatbot and will be asked to enquire their daily life problems related to diabetes. They will also be asked to review the replies of the Chatbot after their interaction.

Outcome Measures

Primary Outcome Measures

  1. Usability of the Chatbot for diabetic patient [One time]

    To assess the usability of the Chatbot, we will employ the mHealth App Usability Questionnaire (MAUQ) to gather feedback from patients following their interaction. Our study will utilize Table 4 of this questionnaire, which consists of three sections: ease of use, interface, and satisfaction and usefulness. Specifically, we will focus our evaluation on 10 out of the 18 questions presented in this table. The selected questions are S1, S2, S6, S7, S9, S11, S12, S13, S14, and S18. Patients will provide their responses on a scale of 1 to 5, where "1" indicates very poor and "5" denotes very good.

  2. Internet Speed [One time]

    Minimum downloading speed of internet will be measured during the chat. This will be recorded in Mega bits per second.

Secondary Outcome Measures

  1. Analyzing Chat response generated by AI Chatbot [One time]

    Likert scale will be used to evaluate the chat response of Chatbot. The following parameters will be evaluated by the specialists for each response namely Clear, Complete and Correct. Clear and Completeness will be evaluated on a range of 1-5, where 1 means poor quality and 5 means very good quality response. The correctness of each response will be further analyzed as Safe and latest. It will be evaluated in binary terms i.e. Yes or No.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Present physically in Pakistan

  • Adults (18 years or older)

  • Diabetic Patient

Exclusion Criteria:
  • Adults unable to consent

  • Individuals who are not yet adults (infants, children, teenagers)

  • Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 CDLE, PCSIR Lbas Complex Karachi Sindh Pakistan

Sponsors and Collaborators

  • Pakistan Council of Scientific and Industrial Research

Investigators

  • Principal Investigator: Ghulam Mustafa, Pakistan Council of Scientific and Industrial Research

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pakistan Council of Scientific and Industrial Research
ClinicalTrials.gov Identifier:
NCT05883072
Other Study ID Numbers:
  • AI Chatbot Evaluation
First Posted:
May 31, 2023
Last Update Posted:
Jun 5, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 5, 2023