- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07379086
Determinants of Primary Care Health Professionals' Numeracy Skills and Practices and Association With Patient Health Literacy and Quality of Care (Num-Pro-Qual)
January 23, 2026 updated by: MSPU de Pins-Justaret
To enable appropriate risk representation for patients, health care professionals (HCPs) must have a personal understanding of quantitative data.
To date, a limited number of studies on physicians' numeracy skills and practices show that, although physicians perform better than the general population, not all physicians have mastered basic numeracy skills.
Low numeracy among physicians was associated with lower quality adherence to good practice recommendations, inaccurate inferences about test results and side effect risks, and reluctance to share numerical information with patients.
The primary objective will be to explore the determinants of the objective numeracy level of primary care professionals.
A cross-sectional survey will be conducted on a sample of primary care professionals practicing in the west of Occitanie (former Midi-Pyrenées region).
Objective numeracy will be measured using the Adaptive Berlin Numeracy Test (ABNT) and the Abbreviated Numeracy Scale, whereas subjective numeracy will be assessed using the Subjective Numeracy Scale (SNS-3).
The Health Literacy Questionnaire (HLQ) will be used for patients.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
500
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
General population
Description
Inclusion criteria:
- Patients over 18 years of age
- having declared one of the participating general practitioners as their treating physician
- declaring to be regularly followed by one of the participating physicians (at least 2 consultations in the last 12 months) for whom a non-opposition collection was carried out
Exclusion criteria:
- diagnosis of major cognitive impairment
- lack of mastery of the French language or lack of ability to understand oral or written instructions
- patient under legal protection regime
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Objective numeracy
Time Frame: Baseline
|
Objective numeracy, as measured by the Adaptive Berlin Numeracy Test (ABNT)
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2026
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
November 15, 2027
Study Registration Dates
First Submitted
January 23, 2026
First Submitted That Met QC Criteria
January 23, 2026
First Posted (Actual)
January 30, 2026
Study Record Updates
Last Update Posted (Actual)
January 30, 2026
Last Update Submitted That Met QC Criteria
January 23, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- Num-Pro-Qual
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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