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A feasibility study of the management of pediatric postoperative pain via mobile phone platform

A feasibility study of the management of pediatric postoperative pain via mobile phone platform

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081044
Enrollment
Unknown
Registered
2024-02-21
Start date
2024-02-22
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

postoperative pain

Interventions

Observation group (using smartphone platform to track, provide feedback and push postoperative pain related information):None

Sponsors

Childrne's Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.1 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1, pediatric patients aged between 1 months and 18 years 2, pediatric patients undergoing elective surgery 3, the patients are sent back to the general ward after surgery 4, the ASA classification grade of the patient is between I-II 5, the patient is predicted to stay in the hospital at least three days after surgery

Exclusion criteria

Exclusion criteria: 1, the proxy with hearing or visual impairment 2, pediatric patients with chronic pain history 3, the patient who deny to participate

Design outcomes

Primary

MeasureTime frame
the proportion of the parents who are willing to manage operative pain via smartphone platform;

Secondary

MeasureTime frame
the response rate of the parents who report the pain level via phone;the associated factors ;the owning rate and utilization of phone among the parents;the consistency of the pain level that reported by the parents via phone and that assessed by the healthcare workers ;

Countries

China

Contacts

Public ContactYun Shi

Children's Hospital of Fudan University

shi_yun@fudan.edu.cn+86 139 1826 8351

Outcome results

None listed

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