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Study on the Clinical Effect of the "Shoushu Feichang Zhun" Mobile Application

Study on the Verification of Clinical Effectiveness of the "Shoushu Feichang Zhun" Mobile Application

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115117
Enrollment
Unknown
Registered
2025-12-23
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Patients are indicated for surgery

Interventions

patient intervention group:the utilization of the "Shoushu Feichang Zhun" (literally meaning "Surgery is Highly Precise") mobile mini-program
patient control group:None
healthcare provider group:None
caregiver control group:None
caregiver intervention group:the utilization of the "Shoushu Feichang Zhun" (literally meaning "Surgery is Highly Precise") mobile mini-program

Sponsors

The Third Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Inclusion Criteria for Patients: 1) Adult patients (aged 18-65 years) scheduled for elective gynecological surgery; 2) Patients who are conscious, capable of understanding the study content, and able to provide informed consent;3) Accompanied by an immediate family member; 4) Patients who own a smartphone and have basic operational skills (or whose family members can operate it on their behalf). 2.Inclusion Criteria for Healthcare Providers 1) Possess a valid Practicing Physician Certificate or Practicing Nurse Certificate, with a registered professional scope consistent with the field covered by this study; 2) Surgeons must have at least 3 years of experience as independent attending surgeons in elective gynecological surgeries; anesthesiologists must have at least 3 years of experience in anesthesia management for gynecological surgeries; operating room nurses must have at least 2 years of experience in nursing collaboration for gynecological surgeries, and have participated in the diagnosis/treatment or nursing of no less than 20 similar surgeries within the past year; 3) Be able to fully understand the core requirements of the study protocol, proficiently operate electronic documentation tools, and possess basic doctor-patient communication skills; 4) Commit to full participation in study training, strict implementation of the group intervention protocol, and completion of data recording and submission in accordance with requirements.

Exclusion criteria

Exclusion criteria: 1.Exclusion Criteria for Patients 1) Severe visual, auditory, or cognitive impairments that affect the use of the mini-program or completion of questionnaires; 2) Comorbidity with mental illnesses such as depression or schizophrenia; 3) Scheduled for emergency surgery or ambulatory outpatient minor surgery; 4) Severe organ dysfunction or failure involving the heart, liver, lungs, or kidneys. 2.Exclusion Criteria for Healthcare Providers 1) Non-permanent practicing staff of the hospital; or those who plan to take leave, transfer positions, or study outside the hospital during the study period and cannot guarantee the diagnosis/treatment or nursing collaboration for at least 8 enrolled patients; 2) Voluntarily request to withdraw from the study; 3) Unable to continue performing research responsibilities due to objective reasons such as personal health conditions or career changes.

Design outcomes

Primary

MeasureTime frame
baseline anxiety score;

Countries

China

Contacts

Public ContactChaojin Chen

The Third Affiliated Hospital Sun Yat-sen University

chenchj28@mail.sysu.edu.cn+86 134 3032 2182

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026