Table 3.
Study methodologies.
| Author/Year | Duration | Key inclusion criteria | Key exclusion criteria | Data collection/analysis summary |
|---|---|---|---|---|
| Wang 2025b (32) | 1 month | Hypertension diagnosis, smartphone use, consent to 1-month intervention | Secondary hypertension, unable to follow up, concurrent treatment/trials, refusal of consent | Collected passive digital phenotypes and uploaded BP/heart rate data; usability assessed with MAUQ and DSSQ; analyzed in SPSS and R using t-tests, Mann–Whitney U, chi-square, and Fishers exact tests. |
| Ho 2025 (34) | 12 months | Adults 18 to <90 years with one cardiovascular condition, prescribed medication in prior 100 days, refill gap of 7 days | No phone listed, hospice/palliative care, non-English/Spanish speakers, outside Colorado/homeless, pregnancy | Patients were identified from pharmacy data, then randomized; primary outcome was refill adherence (PDC) over 365 days, with secondary analysis of refill gap length. |
| Wang 2025a (26) | 6- and 12-month follow-up | Adults 21 + with hypertension, with/without hyperlipidemia, enrolled in program or usual care | Prediabetes, diabetes, stroke, ischemic heart disease, nephritis, nephrosis | Compared program vs. usual care using BP, demographic, health care use, and cost data; used patient-level economic evaluation, regression, and exact matching. |
| Sakane 2023 (28) | 12 weeks | Adults 40–64 years, BMI 25+, BP threshold met, smartphone users able to install apps and communicate online | Already receiving SHG, taking antihypertensives, contraindications to diet/exercise, pregnancy/breastfeeding, severe psychiatric disorders | Used Bluetooth devices, web questionnaires, app assessments, chatbot quizzes, and upload frequency to measure adherence and health outcomes. |
| Echeazarra 2021 (29) | 2 years (2018–2020) | Adults 18 + with hypertension/suspected hypertension, home BP device, smartphone with internet, WhatsApp/Telegram ability, consent | Severe psychiatric disorder, severe illness, clotting disorders, motor/visual disability | Randomized trial comparing bot vs. paper records; assessed BP self-monitoring knowledge, satisfaction, and ambulatory BP outcomes. |
| AlFraidan 2025 (27) | 90 days | Not specified | Not specified | Qualitative case study with daily AI interactions, self-reports, BP readings, thematic analysis, repeated-measures ANOVA, paired t-tests, correlation, and dynamic regression. |
| Antia 2025 (25) | 3 months, 10 days | Hypertension diagnosis, personal Android phone, regular clinic follow-up | No internet-enabled compatible phone, not an active internet user, poor clinic adherence | Single-arm trial with baseline and follow-up questionnaires, repeated BP readings, usability/satisfaction questionnaires, paired t-tests, and regression. |
| Lee 2022 (31) | Nov 2019-Feb 2022 | Hypertension diagnosis, University of Pennsylvania Health System employee, at least one in-person visit, text messaging use | Non-employees, unable/unwilling to use text-based monitoring, seeking care for non-hypertension conditions | Built a chatbot clinician model using iterative innovation; trained on 369 patient messages and scripted automated responses. |
| Rekha 2024 (30) | 4 months | Patients with diabetes, hypertension, or thyroid disorders, age >18, willing to participate | Unwilling participants, psychiatric patients unable to complete questionnaires, pregnancy, breastfeeding, paediatrics | Reviewed prescriptions and interviews to identify drug-related problems using ChatGPT, Naranjo scale, and Hartwig scale; data analyzed in Excel and Prism. |