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Prospective Clinical Validation Study of a Traditional Chinese Medicine Intelligent Inquiry System in Real-World Outpatient Settings

Prospective Clinical Validation Study of a Traditional Chinese Medicine Intelligent Inquiry System in Real-World Outpatient Settings

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123912
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

None

Interventions

Observation group:None

Sponsors

Guangdong Provincial Second Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18–75 years old; 2. Receiving treatment at the Acupuncture and Rehabilitation Department outpatient clinic of the Second Hospital of Guangdong Province during the study period; 3. Able to communicate in Chinese, understand the study instructions, and complete a research questionnaire; 4. No minimum educational requirement, but must have basic reading, comprehension, and expression abilities; 5. Able to operate a smartphone independently; 6. Voluntarily participate in the study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of life-threatening emergencies that require immediate priority treatment, such as chest pain, significant difficulty breathing, active bleeding, persistent high fever with altered consciousness, etc.; 2. Presence of any consciousness disorder; 3. Presence of clear cognitive impairment, disorientation, severe psychiatric abnormalities, or significant difficulties in listening, speaking, reading, or writing that prevent understanding the study content or completing the questionnaire; 4. Those with a history of mild cognitive decline can only be included if the researcher confirms that they can fully understand the study and complete the questionnaire stably; 5. The chief complaint is not within the current support scope of the system; 6. Previously participated in this study; 7. Other situations deemed unsuitable for inclusion by the researcher.

Design outcomes

Primary

MeasureTime frame
Participant-level major omission rate of the system;

Secondary

MeasureTime frame
Completeness rate of key inquiry elements;Red-flag capture rate;Quality score of structured documentation;Terminology standardization score;Participant completion time and additional waiting time;Patient acceptability;

Countries

China

Contacts

Public ContactXiangfeng Chi

Huangpu Hospital, Guangdong Second Traditional Chinese Medicine Hospital

1109884975@qq.com+86 20 8348 2172

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026