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Nationwide Implementation of Standardized Structured Reporting

NCT03649126 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2018-08-28

No results posted yet for this study

Summary

The first objective is to explore factors that impede or facilitate implementation of SSR in pathology (and other disciplines) among the MDT members receiving SSRs. The second objective is to select, develop and evaluate (process and effect outcomes) implementation tools supporting optimal implementation of SSR in pathology. The third objective is to offer implementation tools to all pathology laboratories in the Netherlands and to share the SSR-kit for successful implementation with other medical disciplines

Conditions

  • Standardized Structured Reporting

Interventions

BEHAVIORAL

Implementation tools

Implementation tools developed by experts in order to increase the use of SSR in pathology

Sponsors & Collaborators

  • Dutch Cancer Society

    collaborator OTHER

  • PALGA foundation

    collaborator OTHER

  • Radboud University Medical Center

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
68 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-08-21
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03649126 on ClinicalTrials.gov