- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT04190901
Effect of Physician Race and Gender on Simulated Patients' Ratings
Effect of Physician Race and Gender on Simulated Patients' Ratings and Confidence in Their Physicians: A Randomized Trial
The purpose of the study was to determine whether the race and gender of a simulated doctor affected analog patients' reported confidence and satisfaction in the simulated doctor's diagnosis and treatment plan. The study used two randomized patient analog experiments.
This study is complete and pre-analysis plans (PAPs) for each experiment were published prior to data collection. The PAPs are available at: http://aspredicted.org/blind.php?x=43xj25 (Study 1) and https://aspredicted.org/blind.php?x=369st7 (Study 2).
Przegląd badań
Status
Szczegółowy opis
Prior literature is unclear on whether patients display bias in their evaluations of physicians based on their race or gender. The investigators estimated the effects of physician race and gender using an online clinical vignette. Participants played the role of analog patients reporting to the Emergency Department (ED) with symptoms consistent with gastroenteritis. Participants were provided with a diagnosis of gastroenteritis by a simulated ED physician. The race (black or white) and gender (male or female) of the simulated physician was randomly assigned in a 2x2 factorial experiment. Simulated physicians provided a diagnosis of gastroenteritis and contradicted by an Online Symptom Checker. Following the physician's diagnosis and contradiction by the Online Symptom Checker, participants rated the simulated physician on survey measures of satisfaction and confidence in both the treatment plan and diagnosis. The main (null) hypothesis tested was that there were no differences across the four treatment arms (Black Female, Black Male, White Female, White Male). Participants for the first experiment (Study 1) were recruited from Amazon Mechanical Turk (MTurk) and participants for the second experiment (Study 2) were recruited from Lucid.
Primary Aim: To determine whether the race and gender of a simulated physician had a causal effect on participants' confidence and satisfaction in the physician's diagnosis and treatment plan in an ED setting.
Exploratory Aims: To determine whether the race and gender of a simulated physician had a casual effect on participants' perceptions of the warmth and competence of the physician, their willingness to sue or complain about the physician for an incorrect diagnosis, and their perceived fairness of the charge for the visit.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
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Connecticut
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New Haven, Connecticut, Stany Zjednoczone, 06520
- Yale University
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Adults over 18 years old
Exclusion Criteria:
- Participants who reported current pregnancy
- Participants who reported a current or prior diagnosis of cancer
- Participants who reported a history of abdominal surgery
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Badania usług zdrowotnych
- Przydział: Randomizowane
- Model interwencyjny: Przypisanie czynnikowe
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Simulated Black Male Physician
Participants are randomized to view the clinical vignette with a simulated Black Male physician.
|
Participants in this arm of the experiment viewed one of 10 randomly selected possible images of a simulated Black Male physician.
This image was paired with a written treatment and diagnosis of gastroenteritis alongside a contradictory diagnosis and treatment plan for appendicitis from an Online Symptom Checker.
|
|
Eksperymentalny: Simulated Black Female Physician
Participants are randomized to view the clinical vignette with a simulated Black Female physician.
|
Participants in this arm of the experiment viewed one of 10 randomly selected possible images of a simulated Black Female physician.
This image was paired with a written treatment and diagnosis of gastroenteritis alongside a contradictory diagnosis and treatment plan for appendicitis from an Online Symptom Checker.
|
|
Eksperymentalny: Simulated White Male Physician
Participants are randomized to view the clinical vignette with a simulated White Male physician.
|
Participants in this arm of the experiment viewed one of 10 randomly selected possible images of a simulated White Male physician.
This image was paired with a written treatment and diagnosis of gastroenteritis alongside a contradictory diagnosis and treatment plan for appendicitis from an Online Symptom Checker.
|
|
Eksperymentalny: Simulated White Female Physician
Participants are randomized to view the clinical vignette with a simulated White Female physician.
|
Participants in this arm of the experiment viewed one of 10 randomly selected possible images of a simulated White Female physician.
This image was paired with a written treatment and diagnosis of gastroenteritis alongside a contradictory diagnosis and treatment plan for appendicitis from an Online Symptom Checker.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Patient Confidence
Ramy czasowe: Approximately 10 minutes
|
|
Approximately 10 minutes
|
|
Believed Symptom Checker over Doctor
Ramy czasowe: Approximately 10 minutes
|
"Which diagnosis do you think is more likely to be correct?"
[the doctor's diagnosis (0); online symptom checker (1)]
|
Approximately 10 minutes
|
|
Likelihood of Requesting more Tests
Ramy czasowe: Approximately 10 minutes
|
"Would you ask the doctor to perform additional diagnostic tests?
(Such as the CT scan recommended by the Symptom Checker)."
[definitely not (1); probably not (2); might or might not (3); probably (4); definitely (5)]
|
Approximately 10 minutes
|
|
Patient Satisfaction: scale
Ramy czasowe: Approximately 10 minutes
|
"What number would you use to rate your care during this emergency room visit?" Study 1: [0 (worse possible care) to 100 (best possible care)] Study 2: [0 (worse possible care) to 10 (best possible care)]* *In Study 1, the Patient Satisfaction was measured using a 0-100 point scale. In Study 2, this was measured using a 10 point scale. For all analyses, this Patient Satisfaction outcome from Study 1 was rescaled to match the 0-10 point range in Study 2. |
Approximately 10 minutes
|
|
Likelihood to Recommend
Ramy czasowe: Approximately 10 minutes
|
"Would you recommend this doctor to your friends and family?"
[definitely not (1); probably not (2); might or might not (3); probably (4); definitely (5)]
|
Approximately 10 minutes
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Warmth and Competence
Ramy czasowe: Approximately 10 minutes
|
|
Approximately 10 minutes
|
|
Willingness to sue or complain
Ramy czasowe: Approximately 10 minutes
|
"You take the doctor's advice and go home. Over the next few days, the pain in your abdomen got worse and you returned to the hospital where you were diagnosed with appendicitis. Your appendix had burst and you developed a serious infection. This required emergency surgery and an extended stay in the hospital's intensive Care Unit"*
|
Approximately 10 minutes
|
|
Fairness of the cost
Ramy czasowe: Approximately 10 minutes
|
"You would be charged about $350 for this emergency department visit. How fair do you think this charge is?" [0 = "Completely unfair" to 100 = "Completely Fair"]* *Fairness of the cost was only measured in Study 1. |
Approximately 10 minutes
|
Współpracownicy i badacze
Sponsor
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Inne numery identyfikacyjne badania
- 2000022317
- 12916 (AsPredicted.org)
- 9068 (Inny identyfikator: AsPredicted.org)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Ramy czasowe udostępniania IPD
Kryteria dostępu do udostępniania IPD
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ICF
- ANALITYCZNY_KOD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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