NCT00595218

Brief Summary

Limited data exists for the cancer patients' preferences on their patient-doctor interaction with their radiation oncologist. These physicians have the opportunity to develop intimate relationships with their patients since these patients typically require daily radiation treatments anywhere from one to seven weeks. Thus, by having a greater understanding of the individual patient preferences, the radiation oncologists will be able to better serve their patients leading to improved patient satisfaction with their physician and healthier outlook on life. This is the premise and the hypothesis of this study.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for not_applicable breast-cancer

Timeline
Completed

Started Apr 2006

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2006

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

January 4, 2008

Completed
12 days until next milestone

First Posted

Study publicly available on registry

January 16, 2008

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2008

Completed
Last Updated

July 25, 2017

Status Verified

July 1, 2017

Enrollment Period

2 years

First QC Date

January 4, 2008

Last Update Submit

July 21, 2017

Conditions

Keywords

Patient PreferencesPatient SatisfactionPatient-Doctor Relationship

Outcome Measures

Primary Outcomes (1)

  • Did knowledge of patient preference improve patient satisfaction

    Length of radiation treatment

Secondary Outcomes (1)

  • Patient preferences regarding their radiation oncologists

    Length of radiation treatment course

Study Arms (2)

1

NO INTERVENTION

Patients whose radiation oncologist are blinded to their patient preference survey results

2

ACTIVE COMPARATOR

Patients whose radiation oncologist are not blinded to their patient preference survey results

Behavioral: Physician behavior related to Patient Preference SurveyOther: Patient Preference Results

Interventions

Access to initial Patient preference survey results

2

Knowledge of Patient Preference Results

2

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patient/subject must receive radiation treatment in addition to consultation with the Radiation Oncologist
  • Patient/subject must meet with radiation oncologist at least one day per week while receiving radiation therapy.
  • Any attending radiation oncologist whose patient is enrolled in this study

You may not qualify if:

  • Patient/subject under age 18 If subject previously underwent this study, even if the previous study was for a different diagnosis. Subjects can only undergo this study once.
  • Patients/subjects who do not have the functional and mental capacity to independently answer the questionnaire.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UPMC Cancer Centers

Pittsburgh, Pennsylvania, 15213, United States

Location

MeSH Terms

Conditions

Breast NeoplasmsProstatic NeoplasmsLung NeoplasmsPatient PreferencePatient Satisfaction

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesGenital Neoplasms, MaleUrogenital NeoplasmsGenital Diseases, MaleGenital DiseasesUrogenital DiseasesProstatic DiseasesMale Urogenital DiseasesRespiratory Tract NeoplasmsThoracic NeoplasmsLung DiseasesRespiratory Tract DiseasesTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Ajay Bhatnagar, MD

    University of Pittsburgh

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PI Mentor

Study Record Dates

First Submitted

January 4, 2008

First Posted

January 16, 2008

Study Start

April 1, 2006

Primary Completion

April 1, 2008

Study Completion

April 1, 2008

Last Updated

July 25, 2017

Record last verified: 2017-07

Locations