Adverse events analysis as an educational tool to improve patient safety culture in primary care: an experimental study

The adverse events analysis as an educational tool to improve patient safety culture between family physicians in primary care: an experimental unifactorial controlled randomised multicentre trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN41911128

Enrollment

108

Registered

2011-02-07

Start date

2009-01-01

Completion date

Unknown

Last updated

2020-03-03

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

Conditions

Patient safety culture Not Applicable

Interventions

Residents and their respective tutor (tutor-resident pair) in teaching units on Family and Community Medicine throughout Galicia will be invited to participate. Tutor-resident pairs that agree to part

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Tutors and residents in Family and Community Medicine in last year of studies in Galicia, Spain

Exclusion criteria

Exclusion criteria: Unwilling to participate

Design outcomes

Primary

Measure	Time frame
The dependent variable will be patient safety culture as measured by the Hospital Survey on Patient Safety Culture (SOPS). The independent or explanatory variable will be participation in the intervention - training workshops, recording of adverse events in daily work and reception of feedback. First round SOPS (3-6 months) and second round SOPS (9-12 months).	—

Secondary

Measure	Time frame
Reliability (internal consistency, repeatability), validity (content, criteria, construct) and change sensitivity (size of effect, paired t) of the Hospital Survey on Patient Safety Culture First round SOPS (3-6 months) and second round SOPS (9-12 months).	—

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 28, 2026