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Reliability and validity test and utility parameters development of an electronic patient-reported outcome (PRO)-based perioperative symptom scale for gynecological diseases patients: a multicentre, prospective, observational cohort study

Longitudinal study based on electronic intelligent platform and patient-reported outcomes after gynecological surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114547
Enrollment
Unknown
Registered
2025-12-15
Start date
2025-12-15
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

gynecological diseases

Interventions

reliability and validity verification:None
longitudinal cohort study:None

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are initially diagnosed with primary gynecological diseases and scheduled to undergo surgery.

Exclusion criteria

Exclusion criteria: Patients who are aged < 14 years or have cognitive impairment, nable to complete the scale.

Design outcomes

Primary

MeasureTime frame
Gynecological diseases perioperative symptom scale;Symptom burden;—

Countries

China

Contacts

Public ContactQu Dacheng

Affiliated Hospital of North Sichuan Medical College

qdc3253859@163.com+86 138 9074 5770

Outcome results

None listed

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