Study Protocol for the Effects of Artificial Intelligence (AI)-Supported Automated Nutritional Intervention on Glycemic Control in Patients with Type 2 Diabetes Mellitus
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Nutritional intervention is effective in improving glycemic control in patients with type 2 diabetes but requires large inputs of manpower. Recent improvements in photo analysis technology facilitated by artificial intelligence (AI) and remote communication technologies have enabled automated evaluations of nutrient intakes. AI- and mobile-supported nutritional intervention is expected to be an alternative approach to conventional in-person nutritional intervention, but with less human resources, although supporting evidence is not yet complete. The aim of this study is to test the hypothesis that AI-supported nutritional intervention is as efficacious as the in-person, face-to-face method in terms of improving glycemic control in patients with type 2 diabetes.
This is a multicenter, unblinded, parallel, randomized controlled study comparing the efficacy of AI-supported automated nutrition therapy with that of conventional human nutrition therapy in patients with type 2 diabetes. Patients with type 2 diabetes mainly controlled with diet are to be recruited and randomly assigned to AI-supported nutrition therapy (n = 50) and to human nutrition therapy (n = 50). Asken, a mobile application whose nutritional evaluation has been already validated to that by the classical method of weighted dietary records, has been specially modified for this study so that it follows the recommendations of Japan Diabetes Society (total energy restriction with proportion of carbohydrates to fat to protein of 50–60, 20, and 20–30%, respectively).
The primary outcome is the change in glycated hemoglobin levels from baseline to 12 months, and this outcome is to be compared between the two groups. The secondary outcomes are changes in fasting plasma glucose, plasma lipid profile, body weight, body mass index, waist circumference, blood pressures, and urinary albumin excretion. The results of this randomized controlled trial will fill the gap between the demand for support of AI in nutritional interventions and the scientific evidence on its efficacy.
KeywordsArtificial intelligence (AI) Behavior change Nutritional therapy Remote healthcare
Successful diabetes care requires not only the proper medications but also lifestyle modifications in terms of diets and activity [1, 2]. Among the variety of weight loss methods and multifaceted interventions on lifestyle, nutritional intervention has the largest statistically significant effect on glycemic control in patients with type 2 diabetes . Due to the progressive nature of type 2 diabetes , early nutritional interventions, such as before insulin injections are needed, may be very effective . Prior studies demonstrating significant decreases in glycosylated hemoglobin (HbA1c) during a 1-year nutritional intervention involved frequent contact between patients and registered dietitians, with, for example, patients seen individually on a weekly basis in the Look AHEAD trial  and on a once-monthly basis in the MÈDITA Randomized Trial . Such intense interventions are difficult to maintain in clinical settings because both patients and providers report lack of time  and healthcare resources are limited .
Recent technologies for remote healthcare has a potential to reduce the burden of both patients and healthcare providers regarding dietary management [10, 11]. Patients can make daily dietary records using mobile devices and communicate online with dieticians without the need for hospital visits. Dietary self-monitoring in itself is considered to be an effective strategy for effecting behavior change , and adherence to dietary self-monitoring is higher when an electronic diary is used than when paper records are kept with or without feedbacks . Moreover, improvements in photo analysis technology that often includes artificial intelligence AI) has enabled the automatic identification of food items and evaluation of their nutritional values, by which real-time dietary feedbacks are provided . AI- and mobile-supported nutritional intervention is expected to overcome time and location barriers in human interventions and boost the motivation of patients with type 2 diabetes to adhere to their diet.
With this background, our aim is to demonstrate the efficacy of automated nutritional intervention by use of a mobile phone and AI on reducing glycemia in patients with type 2 diabetes. In the study described here, we adopt a mobile application whose nutritional evaluation has been already validated to that by the classical method of weighted dietary records . The hypothesis of this study is that AI-supported nutritional intervention is as efficacious as in-person, face-to-face method in improving glycemic control in patients with type 2 diabetes.
This is a multicenter, unblinded, parallel, randomized controlled study aimed at comparing the efficacy of AI-supported automated nutrition therapy with that of conventional human nutrition therapy in patients with type 2 diabetes. The study protocol was approved by the Institutional Review Board of Kanazawa University on April 13, 2018 (IRB no. 2623-3); all recruited patients are required to provide written informed consent. This trial is registered in the University Hospital Medical Information Network (UMIN-CTR; https://www.umin.ac.jp/ctr; UMIN ID: UMIN000032231), and is being conducted in accordance with the Declaration of Helsinki of 1964, as revised in 2013. Patient recruitment commenced on April 13, 2018 and is scheduled to continue through to April 13, 2020.
Study Setting and Participants
Participants are recruited from patients attending the outpatient clinics of the Department of Diabetes and Endocrinology at Kanazawa University Hospital, Hokuriku Central Hospital, and Houju Memorial Hospital. Those patients who are obese or overweight and have type 2 diabetes mainly controlled with diet are eligible.
Inclusion criteria are (1) age ≥ 20 years; (2) body mass index (BMI) cutoff for Asians of > 23 kg/m2, which is the World Health Organization cutoff for Asians requiring public health action ; (3) physician diagnosis of type 2 diabetes confirmed by clinical data (e.g., documentation of fasting plasma glucose [FPG] of ≥ 126 mg/dL, a positive oral glucose tolerance test of > 200 mg/dL, or HbA1c ≥ 6.5%); (4) owning and using a mobile phone in their daily lives; and (5) able to understand study procedures and provide written informed consent.
Exclusion criteria include (1) use of insulin and/or glucagon-like peptide-1 within the past 6 months; (2) use of agents causing weight loss; (3) HbA1c ≥ 7.5%; (4) renal dysfunction (e.g., urinary protein > 1 g /g creatinine and/or an estimated glomerular filtration rate of < 45 mL/min/1.73 m2); (5) uncontrolled thyroid disease; (6) uncontrolled hypertension (diastolic blood pressure > 100 mm Hg and/or systolic blood pressure > 160 mm Hg) and/or secondary hypertension; (7) oral or injected steroid use within the past 3 months; (8) pregnancy or planned pregnancy during the study period; (9) history of myocardial infarction, severe uncontrolled heart failure, unstable angina, transient ischemic attack, or stroke in the past 6 months; (10) receiving treatments for malignancies; (11) diagnosed eating disorder; and (12) medical or psychological condition(s) which would compromise the ability to meet protocol requirements in the opinion of the investigator.
Patients are allocated randomly to either AI- and mobile-supported nutrition therapy or in-person nutrition therapy by human dieticians for 1 year. The principle of nutrition therapy in both interventions is total energy restriction, based on the recommendations of Japan Diabetes Society (JDS), Japan Atherosclerosis Society (JAS), and Japan Society for the Study of Obesity (JASSO); the ideal body weight (IBW) is calculated as IBW = height (m)2 × 22 (kg/m2) [17, 18], and the total dietary energy (kcal/day) is estimated as 25–35 kcal/kg IBW/day. Physicians determine the total dietary caloric intake according to the daily activity of each patient [17, 18]: 25–30 kcal/kg IBW for subjects with low-level activity, 30–35 kcal/kg IBW for subjects with usual-level activity, and ≥ 35 kcal/kg IBW for subjects with heavy-level activity. The recommended macronutrient distribution is set to be 50–60% from carbohydrate sources, ≤ 20% from protein sources, and 20–30% from fat sources .
Experimental Group: AI-Supported Nutrition Therapy
The patients also have access to peer support from other Asken users through the in-app diary function. Weights and steps can be automatically recorded in the app by its data-sharing function with other apps, such as GoogleFit and Apple Healthcare. Patients are instructed to log onto the Asken app and input meals and snacks at least once a week.
Comparison Group: Human Nutrition Therapy
In Japan, nutrition therapy managed by human dietitians is covered by health insurance programs for patients with diabetes. The principle of nutrition therapy of a comparison group is the same as that of the experimental group, namely, total caloric restriction with macronutrient distribution as recommended by the JDS . At baseline, dietitians estimate the current energy and nutrient intakes on a face-to-face interview. Participants and dietitians work together to design feasible strategies to improve dietary habits. Patients are provided with printed materials for describing their plans and recording their meals. After the first interview at baseline, human dietitians continue to evaluate the achievement status of the initial plans based on the paper records and to provide individual feedbacks once or more times within 3 months. Patients have a one-to-one meeting for ≥ 20 mi with a human dietitian during each visit.
The primary outcome of this study is the change in HbA1c levels during 1 year of intervention, with the outcomes to be compared between the two groups. HbA1c is an accepted diagnostic parameter by which to monitor long-term glycemic control . Secondary outcomes are absolute changes in (1) FPG; (2) plasma lipid profile, total cholesterol, triglycerides, high-density lipoproteins, and low-density lipoproteins; (3) body weight, BMI, and waist circumference; (4) systolic and diastolic blood pressure; and (5) urinary albumin excretion. (6) Recorded data on the Asken app (frequencies of log-ons, weight, daily intakes of total energy and nutrients) and (7) costs of the interventions in economic terms are also evaluated.
Blood Sampling and Anthropometric Measurements
Venous blood samples are drawn from the antecubital vein after an overnight fast by a trained nurse and transported to the central laboratory of each hospital for analysis. HbA1c is measured using a high-performance liquid chromatography method. Lipids are measured using enzymatic analytical chemistry methods, and plasma glucose is assessed using the glucose oxidase method. Resting blood pressure is measured in the sitting position with an automatic device after ≥ 5 min of rest. Measurements of BMI and waist circumference are conducted according to published methods .
In principle, treatments for diabetes, hypertension, and dyslipidemia are not changed during the study period in order to avoid effects on the efficacy assessments of this study. If it is inevitable to add a new antidiabetic drug to the treatment regimen, a full description of the change and the reason and timing are described in the case report form (CRF). If insulin therapy is started, the trial will be discontinued at that time.
Data Monitoring and Safety
Clinical data of the participants will be extracted from electronic medical records and anonymously provided on an electronic CRF (eCRF) to the data manager. All entries in the CRFs should be backed up with the relevant source data, including informed consent forms, medical history, laboratory data, and recorded data on the app.
Monitoring of this research will be conducted by Innovative Clinical Research Center, Kanazawa University (iCREK). Monitors will ensure that the investigational team complies with the study protocol and that data and adverse events (AEs) are accurately recorded in the CRFs. Due to the low risk character of the intervention in this study, only spontaneously reported AEs will be reported, and the investigators will immediately take appropriate measures when AEs occur.
The primary endpoint of this study is the change of HbA1c from baseline to endpoint (12 months of intervention). Based on the decrease in HbA1c in prior studies involving mobile-supported interventions , we expect that the mean change in HbA1c level will be 0.3% with a standard deviation of 0.3%. At a significance level of 0.05 and a detection power of 80%, the number of cases per group necessary to reach significant difference in change in HbA1c between two groups is calculated to be 74 cases. Assuming a 20% dropout rate, the target number of cases for each group is 50 cases, with a total of 100 participants in this study.
Randomization and Blinding
We use a web-based computerized blocked randomization with blocks of six to assign participants to either two modes of nutrition therapy. Block randomization is performed in each center separately. Randomization is conducted centrally and independently of investigators, and participants in each group are treated equally by their physicians. Although blinding of medical staff and participants to the study allocation is impossible, staff who are responsible for data collection are blinded.
The primary objective of this study is to confirm that AI-supported, fully-automated nutritional intervention is not be inferior to in-person nutrition therapy by human dieticians with regard to HbA1c change during a 1-year period. Non-inferiority is considered confirmed with the use of a prespecified non-inferiority margin of 0.2%. This is established if the lower limit of the 95% confidence interval of the difference in HbA1c change between the two groups (AI-supported group minus human-supported group) is 0.2%. An independent t test is used to compare the two groups for the change in HbA1c, which is calculated by subtracting the value of the baseline from the value after 1 year of intervention. The changes in secondary continuous outcomes of this study are also analyzed using an independent t test. To account for non-dietary factors, such as the addition of new drugs, compliance to medications, and exercise habits, multiple regression analyses for changes in continuous outcomes are performed using these non-dietary factors as covariates.
To estimate the trajectories of repeated measurements for the study period, we use mixed‐models. Differences between two groups (main effect) and the interaction between study groups and study month are assessed for outcomes, including changes in HbA1c, weight, BMI, lipid parameters, and blood pressure. All mixed models are adjusted for sex, age, baseline weight, and baseline HbA1c. Mixed models enable effective use of all available data even with missing values and, therefore, are considered an intention-to-treat method of analysis. Analyses are conducted using SPSS software version 24.0 for Windows (IBM Corp., Armonk, NY, USA). All tests are conducted as two‐sided α = 0.05, and 95% confidence intervals are calculated.
Participants who discontinue using Asken or to seek advice according to the planned consultations with dieticians will continue to have data collected from their routine diabetes clinic visits, unless they specifically withdraw consent for this study.
Strengths and Limitations
This study is a randomized controlled trial with the aim to assess the efficacy of AI-supported automated nutrition intervention utilizing mobile technology on glycemic control in patients with type 2 diabetes mellitus. The study was designed to fill the information gap between the demand for mobile technologies promoting behavior change in eating habits and the scientific evidence supporting its efficacy compared to the conventional in-person interventions by humans .
The accuracy and validity of dietary evaluation is one of the strengths of this study. The dish-based nutritional evaluation performed by the Asken app has been validated to the weighed dietary records, which is the gold-standard method for individual level dietary assessment . The correlation coefficients between those two methods have been reported to be 0.87 for total energy and ≥ 0.75 for macronutrients, which are comparable or even higher than the correlation coefficients between the weighed dietary records and the food frequency questionnaire . Because Asken has developed this database of > 100,000 food items, which can even differentiate one kind of food at one shop from the similar kind at another place, those who often eat out or eat take-outs can more easily gain access to accurate nutritional evaluations.
Personalization of goal-settings and feedbacks are two additional strengths of AI-supported nutritional intervention and key components for the easy use of healthcare apps [26, 27]. Asken requests each patient to set his/her personalized goal for weight and behavior, and this function is expected to foster the intrinsic motivation, similar to other apps for self-management of chronic diseases [28, 29]. The feedbacks are tailor-made based on the self-tracking data of each individual. Moreover, patients can customize food menus for their preferences, create their own items in the app, and cite a routine menu repeatedly on Asken. In their study analyzing the database from the app “Lose it,” Serrano et al. reported that greater customization of the app is associated with a higher likelihood of engagement with the app and positive health outcomes . Personalization of goals and feedbacks realized by use of AI and mobile technology is in line with the “personalized approach to diabetes management” that was recently highlighted in a joint position statement of the American Diabetes Association and the European Association for the Study of Diabetes .
There are some limitations to this study. First, because participants are limited to those who own and use a mobile phone, the results may not be generalized to generations with relatively lower information and communication technology literacy. Second, people who adhere to the healthcare apps are likely to have a deliberative style rather than intuitive style when making health-related decisions. Third, due to the unblinded design, the patients in the AI arm would know that they are getting the experimental intervention, which may result in better outcomes in the AI intervention than the control. Finally, Asken collects data not only on daily diets but also activities such as step counts. Independent contribution of nutritional intervention is to be evaluated by accounting for the effects of other wearable devices monitoring activities.
The authors thank the participants of the study, Chiyoko Takata and Yukiko Takamiya for their secretarial supports, and Ms. Eri Matsuzaki at Kagawa Nutrition University for her comments on methods.
The study ID number is assigned at the time of registration and is used when handling samples and information related to the study to maintain anonymity. Using the study ID number as a key, electronic medical records, eCRFs, administrative forms, and recorded data on the app are linked. The lists that link study ID numbers to identifying information such as names or other personal identifiers are stored in a separate, locked file with password-protected access systems in an area with a limited access. All records that contain names or other personal identifiers, such as informed consent forms, are stored separately from the study records.
Sponsorship for this study and article processing charges are funded by Public Research of Kanazawa University Hospital. This study is also supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture of Japan (17K09199).
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and given their approval for this version to be published.
MK and TY conceived the study. AN and KY provided advice on the study design and statistical analysis. YG participated in the discussion of study design and wrote the study plan. RO drafted the manuscript and AY critically revised the manuscript. All authors read and approved the final manuscript.
Compliance with Ethics Guidelines
The Institutional Review Board of the Kanazawa University approved the study protocol on April 13, 2018 (IRB no. 2623-3) in accordance with the ethical standards of the Declaration of Helsinki and current legal regulations in Japan. All procedures are in accordance with the ethical standards of the institutional and national committees responsible for human experimentation and with the Helsinki Declaration of 1964, as revised in 2013. Substantial amendments of the study protocol must be approved by the IRBs. The investigator provides each potential subject with an informed consent form that has been approved by the IRB, explains the contents of the study in detail both in writing and orally, and obtains the subject’s written consent of his/her own free will.
Rie Oka has received a speaker fee from Novartis. Takashi Yoneda has received a research grant from Daiichi-Sankyo and speaker fees from Astellas, Novaritis, and Sanofi. Ayaka Yasugi is an employee of WIT Co., Ltd., Japan. Akihiro Nomura, Mitsuhiro Kometani, Yuko Gondoh, and Kenichi Yoshimura have nothing to declare.
Data sharing is not applicable to this article because it describes a study protocol.
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