Effect of Physician Attire on Patients' Preference of Physician
Advanced Cancer Patients' Perception of Physician Compassion and Professionalism - A Randomized, Double Blind, Cross Over Trial
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
If participant agrees to take part in this study, participant will be asked to complete 7 questionnaires. These questionnaires ask about participant's gender, date of birth, ethnicity, marital status, level of education, religion, and information about the disease and treatments participant received. Participant will also be asked about any symptoms participant may be having, how much trust participant has in the medical profession in general, how participant feels about the disease, any depression or anxiety participant may have, and participant's level of hopefulness. These questionnaires should take about 6 minutes to complete.
Participant will be shown 2 videos (each 3 minutes long) and then participant will complete questions about each video. Participant will be asked to rate the doctors participant saw on their professionalism and their compassion.
Caregivers will be required to leave the room or stay silent while the participant is watching the videos.
The total time to watch the videos and complete the second set of questionnaires should be about 7 minutes.
Finally, participant will be asked to complete 3 questionnaires about participant's overall preference for a doctor. These questionnaires will take about 5 minutes to complete.
Length of Study Participation:
Participation in this study is complete after participant answers the final questionnaires.
Overall, this study should take about 30 minutes to complete.
This is an investigational study.
Up to 108 participants will be enrolled in this study. All will take part at MD Anderson.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Texas
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Houston, Texas, Forenede Stater, 77030
- University of Texas MD Anderson Cancer Center
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Advanced cancer diagnosis (locally advanced, recurrent or metastatic disease).
- Patients presenting as follow-ups only at the outpatient Supportive Care Center.
- Age >/= 18 years-old
- English speaking
Exclusion Criteria:
- Altered cognition (as assessed routinely in the Supportive Care Clinic using the Memorial Delirium Assessment Scale (MDAS), with a score of >/= 7/30).
- Patients suffering from a severe psychiatric disorder or condition that would significantly interfere with study participation.
- Patients with hearing and/or visual impairments.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Video 1A
Questionnaires completed at baseline, after each video viewing, and at completion. Participants shown Video 1A or 1B, then shown Video 2A or 2B. |
Participants shown Video 1A or 1B, then shown Video 2A or 2B.
Questionnaires completed at baseline, after each video viewing, and at completion.
Andre navne:
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Eksperimentel: Video 1B
Questionnaires completed at baseline, after each video viewing, and at completion. Participants shown Video 1A or 1B, then shown Video 2A or 2B. |
Participants shown Video 1A or 1B, then shown Video 2A or 2B.
Questionnaires completed at baseline, after each video viewing, and at completion.
Andre navne:
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Eksperimentel: Video 2A
Questionnaires completed at baseline, after each video viewing, and at completion. Participants shown Video 1A or 1B, then shown Video 2A or 2B. |
Participants shown Video 1A or 1B, then shown Video 2A or 2B.
Questionnaires completed at baseline, after each video viewing, and at completion.
Andre navne:
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Eksperimentel: Video 2B
Questionnaires completed at baseline, after each video viewing, and at completion. Participants shown Video 1A or 1B, then shown Video 2A or 2B. |
Participants shown Video 1A or 1B, then shown Video 2A or 2B.
Questionnaires completed at baseline, after each video viewing, and at completion.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Participant's Perception of Physician's Compassion
Tidsramme: 1 day
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Participant's rating of physician's compassion assessed by using a validated 5-item tool consisting of five 0-10 numerical rating scales assessing five dimensions: warm-cold, pleasant-unpleasant, compassionate- distant, sensitive- insensitive, and caring-uncaring. The sum of the five scales gives a final score representing physician's compassion on a scale of 0 to 50. |
1 day
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Participant's Perception of Physician's Professionalism
Tidsramme: 1 day
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Participant's rating of physician's professionalism assessed by using a validated 4-item tool assessing politeness, listening, explaining the condition and treatment to the patient and patient's involvement in treatment decisions. Participant rates from poor-1 to very good-5. The sum of these 4 items gives a final score representing physician's level of professionalism on a scale of 4 to 20. |
1 day
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Ahsan Azhar, MD, M.D. Anderson Cancer Center
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2016-0970
- NCI-2018-01195 (Registry Identifier: NCI CTRP)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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