- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02565017
Examining Patient Preferences About the IBM Watson Oncology Clinical Decision Support System
23 juni 2020 uppdaterad av: Memorial Sloan Kettering Cancer Center
The purpose of this study is to learn what cancer patients think about IBM Watson Oncology.
IBM Watson Oncology is a computer program designed to help inform oncologists about the best chemotherapy choices for their patients.
The investigators will conduct focus groups with cancer patients who have received chemotherapy treatment at MSK in order to understand cancer patients' thoughts about IBM Watson Oncology.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Observationell
Inskrivning (Faktisk)
70
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
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New York
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New York, New York, Förenta staterna, 10065
- Memorial Sloan Kettering Cancer Center
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Testmetod
Icke-sannolikhetsprov
Studera befolkning
MSKCC clinics
Beskrivning
Inclusion Criteria:
- MSKCC patient 18 years or older
Breast, lung, or colorectal cancer MSK patient as per EMR or clinician judgment having either:
- Chemotherapeutic adjuvant or neoadjuvant treatment with the first chemo visit occurring within the past 8 months and primary treatment (i.e., surgery), occurring within the past 6 months)at MSK
- OR chemotherapeutic treatment for metastatic disease with the first chemo visit occurring within the past 8 months at MSK
- OR chemotherapeutic treatment through an on-going MSK clinical trial as per clinician
- Residing in New York metro-area
Exclusion Criteria:
- Non-English speakers because we do not have the resources to conduct and translate the focus groups into other languages
- Patients who are not or will not receive their cancer care at MSKCC.
- Patient unwilling or unable to provide informed consent
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: Kohort
- Tidsperspektiv: Blivande
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
Breast Cancer
and treatment type (chemotherapeutic adjuvant (i.e., chemotherapy delivered after primary therapy/surgery) or neoadjuvant (i.e., chemotherapy delivered prior to primary therapy/surgery) treatment, chemotherapeutic treatment for metastatic disease, or chemotherapeutic treatment through a clinical trial).
|
After the presentation of the of IBM Watson Oncology at the opening of the focus group, participants will be asked to fill out a de-identified brief 15-item questionnaire to assess participants' first impressions of IBM Watson Oncology.
The questionnaire will be self administered, and will take approximately 5 minutes to complete.
Completed questionnaires will be collected by a member of the study staff, and the focus group will proceed with introductions.
The focus group will be audio recorded from the completion of the introductions and notes will be taken.
The focus group guide will address the study aims.
At the end of the focus group, participants will complete a 7-item questionnaire to capture simple demographic information including education, income, and health literacy.
This questionnaire will take 3-5 minutes to complete.
|
|
Lung Cancer
and treatment type (chemotherapeutic adjuvant (i.e., chemotherapy delivered after primary therapy/surgery) or neoadjuvant (i.e., chemotherapy delivered prior to primary therapy/surgery) treatment, chemotherapeutic treatment for metastatic disease, or chemotherapeutic treatment through a clinical trial).
|
After the presentation of the of IBM Watson Oncology at the opening of the focus group, participants will be asked to fill out a de-identified brief 15-item questionnaire to assess participants' first impressions of IBM Watson Oncology.
The questionnaire will be self administered, and will take approximately 5 minutes to complete.
Completed questionnaires will be collected by a member of the study staff, and the focus group will proceed with introductions.
The focus group will be audio recorded from the completion of the introductions and notes will be taken.
The focus group guide will address the study aims.
At the end of the focus group, participants will complete a 7-item questionnaire to capture simple demographic information including education, income, and health literacy.
This questionnaire will take 3-5 minutes to complete.
|
|
Colorectal Cancer
and treatment type (chemotherapeutic adjuvant (i.e., chemotherapy delivered after primary therapy/surgery) or neoadjuvant (i.e., chemotherapy delivered prior to primary therapy/surgery) treatment, chemotherapeutic treatment for metastatic disease, or chemotherapeutic treatment through a clinical trial).
|
After the presentation of the of IBM Watson Oncology at the opening of the focus group, participants will be asked to fill out a de-identified brief 15-item questionnaire to assess participants' first impressions of IBM Watson Oncology.
The questionnaire will be self administered, and will take approximately 5 minutes to complete.
Completed questionnaires will be collected by a member of the study staff, and the focus group will proceed with introductions.
The focus group will be audio recorded from the completion of the introductions and notes will be taken.
The focus group guide will address the study aims.
At the end of the focus group, participants will complete a 7-item questionnaire to capture simple demographic information including education, income, and health literacy.
This questionnaire will take 3-5 minutes to complete.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Acceptability of IBM Watson Oncology
Tidsram: 1 year
|
Data collected through the brief questionnaires (e.g.,initial impressions of IBM Watson Oncology, sociodemographics) will be entered into an SPSS data file on the secure MSK server.
|
1 year
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Användbara länkar
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
15 september 2015
Primärt slutförande (Faktisk)
22 juni 2020
Avslutad studie (Faktisk)
22 juni 2020
Studieregistreringsdatum
Först inskickad
30 september 2015
Först inskickad som uppfyllde QC-kriterierna
30 september 2015
Första postat (Uppskatta)
1 oktober 2015
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
25 juni 2020
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
23 juni 2020
Senast verifierad
1 augusti 2019
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 15-226
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .