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Co-development and testing of a smartphone-based Wechat Mini Program for postoperative pain management in teenagers

Co-development and testing of a smartphone-based Wechat Mini Program for postoperative pain management in teenagers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600132267
Enrollment
Unknown
Registered
2026-09-11
Start date
2026-09-15
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

pain

Interventions

manager:None
healthcare worker:None
caregiver:None

Sponsors

children's hospital of fudan university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Group 1: Patients. Inclusion criteria: 1, pediatric patients undergoing elective major surgery at a pediatric hospital; 2, aged 10–18 years. Group 2: Patient Caregivers. Inclusion criteria: 1. Caregivers of pediatric patients enrolled in the study; 2. Owners of a smartphone who are proficient in using its basic functions; 3. Possess basic literacy skills. Group 3: Healthcare Professionals. Inclusion criteria: Anesthesiologists working in the Department of Anesthesiology at a pediatric hospital with more than 10 years of experience in postoperative pain management for children.

Exclusion criteria

Exclusion criteria: Group 1: Patients. 1. Those with concurrent intellectual disability or cognitive impairment; 2. Those with concurrent severe systemic diseases, such as hepatic or renal insufficiency, respiratory failure, or heart failure; 3. Those admitted to the intensive care unit (ICU) postoperatively; 4. Those who refused to participate in the study. Group 2: Patients’ caregivers. 1. Do not own a smartphone or refuse to use mobile health tools; 2. Have participated in a similar study; 3. Are currently participating in other studies related to pain or mobile health tools; 4. Refuse to participate in the study. Group 3: Healthcare professionals. 1. Refuse to participate in the study.

Design outcomes

Primary

MeasureTime frame
difficulties in pain management;Expectations for Mobile Health Tools;

Countries

China

Contacts

Public ContactShi Yun

children's hospital of fudan university

imulashi@yahoo.com+86 133 7009 8290

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026