Message: Study of Patients' Perception of Physician's Compassion
A Trial on Patient's Evaluation of a Physician Conveying Two Different Messages
Przegląd badań
Szczegółowy opis
If participant agree to take part in the study, basic information will be collected (such as date of birth, date of diagnosis, sex, and religion). Participant will also complete questionnaires about any symptoms they may be having, how hopeful they are, how they are accepting the disease, their trust in the medical profession, and how they like information to be delivered to them.
After completing the questionnaires, they will be randomly assigned (as the roll of dice) to one of 4 groups.
Regardless of which group they are in, they will watch 2 short videos that show actors portraying a doctor and patient having a conversation about treatment options in a clinical setting. Both videos will discuss the same material, but the order of the videos and the actors in the videos will be different for each group. Both videos are about 4 minutes long.
After watching each video, the participant will complete 3 questionnaires about the doctor in the video. It should take about 38 minutes to watch both videos and to complete all of the questionnaires.
After they have watched both videos, they will be asked to choose which doctor they preferred and to briefly explain the reasons why they chose that doctor.
Length of Study:
Participant will be off study after they have completed the last questionnaire.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Texas
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Houston, Texas, Stany Zjednoczone, 77030
- University of Texas MD Anderson Cancer Center
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Diagnosis of advanced cancer, defined as locally advanced, recurrent or metastatic disease
- Patients treated as outpatients by the Supportive and Palliative Care team.
- Age >/= 18 years-old
- English speaking
- Normal cognitive status as determined by the interviewer based on the ability to understand the nature of the study and consent process.
Exclusion Criteria:
1) Patients suffering from a severe psychiatric disorder or condition that would significantly interfere with study participation, as determined by the Principal Investigator or by the attending palliative care physician.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Przydział: Randomizowane
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Aktywny komparator: Group 1: Video/Doctor Sequence 1
Participants watch two videos with varying video/doctor sequence and complete 3 surveys (one before the first video and one survey after each video)
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Watch two short videos with a 4-minute interval between the two of them, estimate 8 minutes to watch both the videos.
One set of surveys before first video and one set after each video played, estimate total of 30 minutes for all surveys.
Inne nazwy:
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Aktywny komparator: Group 2: Video/Doctor Sequence 2
Participants watch two videos with varying video/doctor sequence and complete 3 surveys (one before the first video and one survey after each video)
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Watch two short videos with a 4-minute interval between the two of them, estimate 8 minutes to watch both the videos.
One set of surveys before first video and one set after each video played, estimate total of 30 minutes for all surveys.
Inne nazwy:
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Aktywny komparator: Group 3: Video/Doctor Sequence 3
Participants watch two videos with varying video/doctor sequence and complete 3 surveys (one before the first video and one survey after each video)
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Watch two short videos with a 4-minute interval between the two of them, estimate 8 minutes to watch both the videos.
One set of surveys before first video and one set after each video played, estimate total of 30 minutes for all surveys.
Inne nazwy:
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Aktywny komparator: Group 4: Video/Doctor Sequence 4
Participants watch two videos with varying video/doctor sequence and complete 3 surveys (one before the first video and one survey after each video)
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Watch two short videos with a 4-minute interval between the two of them, estimate 8 minutes to watch both the videos.
One set of surveys before first video and one set after each video played, estimate total of 30 minutes for all surveys.
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Participant's Rating of Physician's Compassion
Ramy czasowe: Approximately 38 minutes for video viewing and surveys.
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Physician compassion tested using compassion data from the first video viewed by each patient as assessed by a Physician Compassion Assessment survey.
Patient's rating of physician's compassion by using a 5-item tool consisting of five 0-10 numerical rating scales assessing five dimensions: warm-cold, pleasant-unpleasant, compassionate-distant, sensitive insensitive, caring-uncaring.
The sum of the five scales will give a final score representing physician's compassion with a 0 to 50 scale.
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Approximately 38 minutes for video viewing and surveys.
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Współpracownicy i badacze
Sponsor
Śledczy
- Krzesło do nauki: Kimberson C. Tanco, MD, M.D. Anderson Cancer Center
Publikacje i pomocne linki
Przydatne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Inne numery identyfikacyjne badania
- 2012-0113
- NCI-2015-01419 (Identyfikator rejestru: NCI CTRP)
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