Post-Hoc Enthusiasm and Wariness

NCT ID: NCT05686889

Last Updated: 2023-01-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-01

Study Completion Date

2028-09-01

Brief Summary

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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.

Detailed Description

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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).

Conditions

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Health Behavior

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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Success

Symptomatic improvement present

Group Type EXPERIMENTAL

Patient self-report

Intervention Type OTHER

Simulated patient following structured script

Failure

Symptomatic improvement absent

Group Type EXPERIMENTAL

Patient self-report

Intervention Type OTHER

Simulated patient following structured script

Interventions

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Patient self-report

Simulated patient following structured script

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Community pharmacist

Exclusion Criteria

* Outside Ontario
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sunnybrook Health Sciences Centre

OTHER

Sponsor Role lead

Responsible Party

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Dr. Don Redelmeier

Senior Scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Donald A Redelmeier, MD, MSc

Role: PRINCIPAL_INVESTIGATOR

Sunnybrook Health Sciences Centre

Central Contacts

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Donald A Redelmeier, MD, MSc

Role: CONTACT

4164806999

Other Identifiers

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5692

Identifier Type: -

Identifier Source: org_study_id

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