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WithdrawnNCT03115528Updated May 22, 2019

Difference in the Estimation of Prognosis

An observational study in Malignant Neoplasms of Independent (Primary) Multiple Sites, sponsored by M.D. Anderson Cancer Center. Withdrawn. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-05-22.

Sponsored by M.D. Anderson Cancer Center · Observational

Why this study was withdrawn
Terminated at Continuing Review
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

Objectives:

Primary Objective:

The primary objective is to identify the difference in the estimation of prognosis of advanced cancer patients between medical oncologists, gynecological oncologists, and palliative care physicians

Read the detailed description

The goal of this research study is to identify the difference in the estimation of prognosis of advanced cancer patients between medical or gynecological oncologists, and palliative care physicians. Up to 140 patients will be enrolled in this study.

02

Conditions studied

  • Malignant Neoplasms of Independent (Primary) Multiple Sites

Keywords

  • Malignant neoplasms of independent (primary) multiple sites
  • Medical oncologists
  • Palliative care physicians
  • Questionnaire
  • Survey
03

In context

Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 3,044 studies on the registry; 578 are open to participants now.

Of its 608 completed or terminated interventional studies of FDA-regulated products, 407 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Medical oncologists and palliative care physicians from UT MD Anderson Cancer Center

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Medical oncologists or gynecological who referred patients to the palliative care team; Palliative Care physicians to whom the patients were referred; Patients with locally advanced, metastatic, or, not curable cancer.
  2. 18 years old or older

Exclusion criteria

Exclusion Criteria:

N/A

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No

Groups and cohorts

  • Medical Oncology Physicians

    Medical oncology physicians are sent the Estimation of Prognosis questionnaire by email.

    Behavioral: Estimation of Prognosis Questionnaire

  • Palliative Care Physicians

    Palliative care physicians are sent the Estimation of Prognosis questionnaire by email.

    Behavioral: Estimation of Prognosis Questionnaire

Interventions

  • BehavioralEstimation of Prognosis Questionnaire

    Survey will examine two aspects of prognosis estimation: 1.) physician factors, 2.) prognosis estimation and contributing factors to patient prognosis. Survey will take approximately 5 minutes to complete.

    Also known as: Survey

06

What researchers measure

Primary outcomes

  1. Estimation of Patient Overall Survival by Oncologists and by Palliative Care Physicians per Estimation of Prognosis Questionnaire

    The answer to the question #4, "How long do you think this patient will live?" in the questionnaire is the primary endpoint. Denoting the oncologist estimated OS time from the day of palliative care consult to death by TOnc, palliative care physician estimate by TPalliative, and the true OS time by T0, we define the accuracy of the estimation of OS by oncologists and by palliative care physician as ΔOnc = TOnc - T0 ΔPalliative = TPalliative - T0. And the difference between these two estimates is calculated as ΔOS = ΔOnc - ΔPalliative. Based on the above formulas, ΔOS is actually calculated as (TOnc- TPalliative). The true survival time, T0, is cancelled out by the subtraction.

    Time frame: 6 weeks

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Study locations

No study locations are listed for this record.

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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03115528
Responsible party
Sponsor
First posted
Apr 14, 2017
Start date
Dec 14, 2017
Primary completion
Dec 2030 (estimated)
Completion
Dec 2030 (estimated)
Last update
May 22, 2019

Study contacts

Angelique N. Wong, MD
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in May 2019. You cannot join it, but the record below documents what was studied.

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