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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05686889
Other study ID # 5692
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date September 1, 2028

Study information

Verified date January 2023
Source Sunnybrook Health Sciences Centre
Contact Donald A Redelmeier, MD, MSc
Phone 4164806999
Email dar@ices.on.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The post-hoc fallacy (also termed the post-hoc-ergo-propter-hoc fallacy) has been recognized for centuries with endless relevance. The general concept in medical care is that patients who improve after a treatment are not necessary patients who improve because of a treatment. Modern medicine provides multiple opportunities to examine such pitfalls of judgment due to the prevailing uncertainty, incompleteness of our understanding pathogenic mechanisms, and natural tendency to connect treatments to outcomes. In this study, we will investigate whether judgments about vitamin supplementation might demonstrate the post-hoc fallacy.


Description:

We plan to conduct a brief survey of pharmacies portraying a patient in two slightly different versions. One version will portray the patient who feels better after starting a vitamin supplement whereas another version will portray the patient who feels unchanged after starting a vitamin supplement. The patients will be randomly assigned to participants and otherwise contain identical information. Judgments will be measured by eliciting participants recommendation about continuing the vitamin (Appendix_Script).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date September 1, 2028
Est. primary completion date September 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Community pharmacist Exclusion Criteria: - Outside Ontario

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Patient self-report
Simulated patient following structured script

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre

Outcome

Type Measure Description Time frame Safety issue
Primary Response variable in each survey is a binary recommendation whether to continue the vitamin supplement or discontinue the vitamin supplement Health provider clinical recommendation Short-term (less than 5 minutes)
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