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Compliance With PROMs Detection Through Digital Support and Correlation Compared Standard to Outpatient Detection in Knee Prosthetics

Study acronym: DIG-PROMs-k
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary completion date: Jan 1, 2026 to Dec 1, 2027
    • Study completion date: Jun 1, 2026 to Dec 31, 2027
    v6
  2. Primary completion date: Jan 1, 2025 to Jan 1, 2026
    • Study completion date: Jun 1, 2025 to Jun 1, 2026
    v5
  3. Re-verified, no change to tracked fieldsv4
  4. Primary completion date: Oct 1, 2022 to Jan 1, 2025
    • Study completion date: Jan 1, 2023 to Jun 1, 2025
    • Study arms: 0 to 1
    v3
  5. Primary completion date: Oct 1, 2021 to Oct 1, 2022
    • Study completion date: Jan 1, 2022 to Jan 1, 2023
    v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Two methods for detecting outcomes after knee prosthetic surgery are compared: the traditional one using paper questionnaires administered in the outpatient setting (Oxford Knee Score) VS detection using digital questionnaires created on Google Forms and sent to the patient's smartphone on which the compilation takes place in the extra area outpatient.
Trial Details
NCT Number NCT04752761
Lead Sponsor Istituto Ortopedico Rizzoli
Conditions
(from sponsor)		 Approach-Approach Conflict, Knee Discomfort
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov