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Message: Study of Patients' Perception of Physician's Compassion

14. juli 2016 opdateret af: M.D. Anderson Cancer Center

A Trial on Patient's Evaluation of a Physician Conveying Two Different Messages

The goal of this study is to learn what types of conversations patients prefer to have with their doctor about treatment options and how patients view their doctor's compassion.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

103

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Texas
      • Houston, Texas, Forenede Stater, 77030
        • University of Texas MD Anderson Cancer Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Diagnosis of advanced cancer, defined as locally advanced, recurrent or metastatic disease
  2. Patients treated as outpatients by the Supportive and Palliative Care team.
  3. Age >/= 18 years-old
  4. English speaking
  5. 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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Tildeling: Randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv 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)
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.
Andre navne:
  • Survey Questionnaires
  • spørgeskema
Aktiv 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)
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.
Andre navne:
  • Survey Questionnaires
  • spørgeskema
Aktiv 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)
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.
Andre navne:
  • Survey Questionnaires
  • spørgeskema
Aktiv 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)
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.
Andre navne:
  • Survey Questionnaires
  • spørgeskema

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Participant's Rating of Physician's Compassion
Tidsramme: Approximately 38 minutes for video viewing and surveys.
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.
Approximately 38 minutes for video viewing and surveys.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Studiestol: Kimberson C. Tanco, MD, M.D. Anderson Cancer Center

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. maj 2013

Primær færdiggørelse (Faktiske)

1. august 2015

Studieafslutning (Faktiske)

1. august 2015

Datoer for studieregistrering

Først indsendt

29. januar 2015

Først indsendt, der opfyldte QC-kriterier

5. februar 2015

Først opslået (Skøn)

6. februar 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

15. juli 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

14. juli 2016

Sidst verificeret

1. juli 2016

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2012-0113
  • NCI-2015-01419 (Registry Identifier: NCI CTRP)

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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