Physician-Patient Communication About Breast Cancer-Related Internet Information and Its Effect on Patient Satisfaction and Anxiety

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborators:
Information provided by (Responsible Party):
Memorial Sloan-Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT00712569
First received: July 7, 2008
Last updated: January 31, 2013
Last verified: January 2013

July 7, 2008
January 31, 2013
June 2008
June 2013   (final data collection date for primary outcome measure)
  • patients in Category 1 (those who have been recorded discussing internet information with their physician) are pt satisfaction & pt anxiety. PT satisfaction with the consultation is an outcome assessed only at the end of the consultation. [ Time Frame: conclusion of the study ] [ Designated as safety issue: No ]
  • To examine the effect of physician responses to cancer-related internet information on patient satisfaction and anxiety. (Category 1 patients). [ Time Frame: conclusion of study ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00712569 on ClinicalTrials.gov Archive Site
To identify cancer patients' reasons for not discussing cancer-related internet information with their physicians. (Category 2 and 3 patients). [ Time Frame: conclusion of study ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Physician-Patient Communication About Breast Cancer-Related Internet Information and Its Effect on Patient Satisfaction and Anxiety
Physician-Patient Communication About Breast Cancer-Related Internet Information and Its Effect on Patient Satisfaction and Anxiety

The purpose of this study is to learn about how patients who have looked up cancer-related information on the internet talk with their doctors. We are interested in these conversations even if the patients do not think they will talk about the information with their doctor during their visit. We will audio record doctor-patient visits and listen to these recordings to learn about how patients who have looked up cancer-related internet information talk to their doctors and how their doctors talk to them. We will also give patients questionnaires before and after their appointments to learn about what they think about communicating with their doctors.

Not Provided
Observational
Observational Model: Case-Crossover
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

physicians at the Breast Service and their patients will be recruited to participate in this study.

Breast Cancer
  • Behavioral: questionnaires
    Patients in Category 1 are those who report before the visit that they intend to discuss cancer-related internet information and report after the visit that they did discuss such information. The coding of these patients' consultations with their physicians and analysis of their pre- and post-consultation questionnaires will address Aims 1 and 2.
  • Behavioral: audio recordings , questionnaires

    Patients in Category 2 are those who report before the visit that they intend to discuss cancer-related internet information, but report after the visit that they did not discuss such information. This category is important as our previous research indicates that sometimes patients do not discuss information because they feel there is not enough time or because the information is irrelevant or repetitive. These patients' audio recordings will be checked to verify that there was no internet information discussion. These audio recordings will not be coded.

    However, assessment of these patients' questionnaires will aid in addressing Aim 3 and may provide some pilot data on why patients who initially intend to discuss internet information do not.

  • Behavioral: audio recorded questionnaires
    Patients in Category 3 are those who report before the visit that they do not intend to discuss cancer-related internet information and do not discuss it. Assessment of these patients' questionnaires will aid in addressing Aim 3. These audio recordings will not be coded. It is important, however, that these consultations be audio recorded for two reasons: First, it allows the physician to remain blinded to the intent of the patient to discuss internet information. Second, it provides a method of verifying that the patient really did not discuss internet information. Although not expected, it is possible for a patient to go into a consultation without intending to discuss internet information, but does end up discussing it. We will note if this occurs.
  • 1
    Patients in Category 1 are those who report before the visit that they intend to discuss cancer-related internet information and report after the visit that they did discuss such information.
    Intervention: Behavioral: questionnaires
  • 2
    Patients in Category 2 are those who report before the visit that they intend to discuss cancer-related internet information, but report after the visit that they did not discuss such information.
    Intervention: Behavioral: audio recordings , questionnaires
  • 3
    Patients in Category 3 are those who report before the visit that they do not intend to discuss cancer-related internet information and do not discuss it.
    Intervention: Behavioral: audio recorded questionnaires
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
85
June 2013
June 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

Subject Inclusion Criteria for Patients

  • Female
  • Diagnosis of breast cancer
  • Pre-surgery (*for breast surgeon patients only)
  • Report that they have read breast cancer-related internet information since their diagnosis with breast cancer.
  • Provide informed consent

Subject Inclusion Criteria Physicians

  • Breast surgeon or breast medical oncologist
  • Agree to participate in study and one of 10 selected participants
  • Provide inform consent

Exclusion Criteria:

Exclusion Criteria for Patients

  • Less than 21 years of age
  • Cognitive or physical impairment rendering patients incapable of providing informed consent to participate in the study
  • As the measures and coding system are all written in English, subjects who are not fluent in English will be excluded.

Exclusion Criteria for Physicians

  • None
Female
21 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00712569
08-079, NIH, NCI, R03 CA130591-01
Not Provided
Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
  • National Institutes of Health (NIH)
  • National Cancer Institute (NCI)
Principal Investigator: Carma Bylund-Lincoln, PhD Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
January 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP