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Randomized Controlled Trial
. 2023 Dec 1;6(12):e2340232.
doi: 10.1001/jamanetworkopen.2023.40232.

Use of Voice-Based Conversational Artificial Intelligence for Basal Insulin Prescription Management Among Patients With Type 2 Diabetes: A Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Use of Voice-Based Conversational Artificial Intelligence for Basal Insulin Prescription Management Among Patients With Type 2 Diabetes: A Randomized Clinical Trial

Ashwin Nayak et al. JAMA Netw Open. .

Abstract

Importance: Optimizing insulin therapy for patients with type 2 diabetes can be challenging given the need for frequent dose adjustments. Most patients receive suboptimal doses and do not achieve glycemic control.

Objective: To examine whether a voice-based conversational artificial intelligence (AI) application can help patients with type 2 diabetes titrate basal insulin at home to achieve rapid glycemic control.

Design, setting, and participants: In this randomized clinical trial conducted at 4 primary care clinics at an academic medical center from March 1, 2021, to December 31, 2022, 32 adults with type 2 diabetes requiring initiation or adjustment of once-daily basal insulin were followed up for 8 weeks. Statistical analysis was performed from January to February 2023.

Interventions: Participants were randomized in a 1:1 ratio to receive basal insulin management with a voice-based conversational AI application or standard of care.

Main outcomes and measures: Primary outcomes were time to optimal insulin dose (number of days needed to achieve glycemic control), insulin adherence, and change in composite survey scores measuring diabetes-related emotional distress and attitudes toward health technology and medication adherence. Secondary outcomes were glycemic control and glycemic improvement. Analysis was performed on an intent-to-treat basis.

Results: The study population included 32 patients (mean [SD] age, 55.1 [12.7] years; 19 women [59.4%]). Participants in the voice-based conversational AI group more quickly achieved optimal insulin dosing compared with the standard of care group (median, 15 days [IQR, 6-27 days] vs >56 days [IQR, >29.5 to >56 days]; a significant difference in time-to-event curves; P = .006) and had better insulin adherence (mean [SD], 82.9% [20.6%] vs 50.2% [43.0%]; difference, 32.7% [95% CI, 8.0%-57.4%]; P = .01). Participants in the voice-based conversational AI group were also more likely than those in the standard of care group to achieve glycemic control (13 of 16 [81.3%; 95% CI, 53.7%-95.0%] vs 4 of 16 [25.0%; 95% CI, 8.3%-52.6%]; difference, 56.3% [95% CI, 21.4%-91.1%]; P = .005) and glycemic improvement, as measured by change in mean (SD) fasting blood glucose level (-45.9 [45.9] mg/dL [95% CI, -70.4 to -21.5 mg/dL] vs 23.0 [54.7] mg/dL [95% CI, -8.6 to 54.6 mg/dL]; difference, -68.9 mg/dL [95% CI, -107.1 to -30.7 mg/dL]; P = .001). There was a significant difference between the voice-based conversational AI group and the standard of care group in change in composite survey scores measuring diabetes-related emotional distress (-1.9 points vs 1.7 points; difference, -3.6 points [95% CI, -6.8 to -0.4 points]; P = .03).

Conclusions and relevance: In this randomized clinical trial of a voice-based conversational AI application that provided autonomous basal insulin management for adults with type 2 diabetes, participants in the AI group had significantly improved time to optimal insulin dose, insulin adherence, glycemic control, and diabetes-related emotional distress compared with those in the standard of care group. These findings suggest that voice-based digital health solutions can be useful for medication titration.

Trial registration: ClinicalTrials.gov Identifier: NCT05081011.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: Drs A. Nayak, Vakili, and Schulman reported owning stock in UpDoc outside the submitted work. UpDoc is an early-stage company that was founded 3 months after this trial was completed and is building solutions for patient engagement broadly related to concepts introduced in this trial; however, this trial did not receive any funding from UpDoc, and UpDoc is not using any of the resources (including software) developed for this trial. UpDoc has filed patents on its technology, from which Drs A. Nayak, Vakili, and Schulman would potentially stand to benefit. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Patient Flow Diagram
HbA1c indicates hemoglobin A1c; VBAI, voice-based conversational artificial intelligence.
Figure 2.
Figure 2.. Number of Insulin Dose Adjustments per Participant Over Time
VBAI indicates voice-based conversational artificial intelligence. aThe median time to optimal insulin dose was 15 days in the VBAI group. Less than 50% of participants achieved optimal insulin dosing in the standard of care group.

References

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