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Empowering rural physicians through an AI-assisted intervention for deprescribing in older adults with comorbid diabetes and hypertension: a feasibility study

Empowering rural physicians through an AI-assisted intervention for deprescribing in older adults with comorbid diabetes and hypertension: a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126204
Enrollment
Unknown
Registered
2026-06-05
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

comorbidity of diabetes and hypertension

Interventions

Rural physicians:Provide an AI agent with functions of clinical medication
Patients:Reduce potentially inappropriate medication(deprescribing)

Sponsors

The Second Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for rural physicians:(1) A minimum of two years of clinical practice in rural primary healthcare institutions; (2) Hold a practicing physician qualification;(3) Currently managing at least 100 patients with concurrent primary hypertension and/or type 2 diabetes mellitus; (4) Demonstrated proficiency in basic computer operations and internet usage. Inclusion criteria for patients:(1) Age 65 years or older; (2) Documented diagnosis of primary hypertension and type 2 diabetes mellitus according to ICD-10 criteria; (3) Currently receiving five or more long-term medications (including both prescription and over-the-counter drugs); (4) Expected to remain in the local area throughout the study period and be available for follow-up visits.

Exclusion criteria

Exclusion criteria: Exclusion criteria for rural physicians:(1) Anticipated resignation or extended leave during the study period; (2) Concurrent enrollment in other clinical research that may confound study outcomes; (3) Refusal to provide written informed consent. Exclusion criteria for patients:(1) Presence of severe cognitive impairment or psychiatric illness precluding study participation; (2) Life expectancy less than 12 months; (3) Acute cardiovascular event or hospitalization for acute exacerbation of chronic disease within the preceding three months; (4) Refusal to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
Total number of medications;

Secondary

MeasureTime frame
Number of potentially inappropriate medications (PIMs) ;Medication Appropriateness Index (MAI) ;Incidence of adverse drug reactions;Blood pressure;Fasting plasma glucose;lycated haemoglobin (HbA1c);Acceptability of Intervention Measure (AIM);Intervention Appropriateness Measure (IAM);Feasibility of Intervention Measure (FIM);

Countries

China

Contacts

Public ContactWu Lingyan

The Second Affiliated Hospital, Zhejiang University School of Medicine

wulingyan@zju.edu.cn+86 571 8776 7089

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026