- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03530969
Geriatric Communication Skills Training Program for Oncology Clinicians
February 19, 2024 updated by: Memorial Sloan Kettering Cancer Center
Geriatric Communication Skills Training Program for Oncology Clinicians to Improve Management of Care for Geriatrics Cancer Patients
The purpose of this study is to learn more about the effects of a training program designed to help doctors communicate better with older patients and their caregivers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
- Behavioral: Self-Efficacy Assessment
- Behavioral: UCLA Geriatrics Attitudes Scale
- Behavioral: Course Evaluations
- Behavioral: The Consultation and Relational Empathy (CARE) questionnaire
- Behavioral: Consumer Assessment of Health Care Providers and Systems Program (CAHPS)
- Behavioral: Patient activation measure (PAM) scale
Study Type
Interventional
Enrollment (Actual)
88
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10065
- Memorial Sloan Kettering Cancer Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
Clinician Eligibility
- MSK medical oncology Health Care Professionals (HCP) - specifically identified as Attendings, fellows, or Advance Practice Professional (APP) - either a Nurse Practitioner (NP) or Physician Assistant (PA) from GI, GU Oncology, Lymphoma, Bone Marrow Transplant or Geriatrics Service (five services with a large number of geriatric patients)
- Willingness to be audio-recorded as per self-report
- Clinician has individual clinic consultations with patients in the target population: 65 years of age and over, English speaking, and patients who have had a new visit within the last 6 months.
Patient Eligibility
- MSK patients 65 years of age and over as per EMR
- English speaking as per EMR
- Being seen by one of the consented HCPs as per the HCP and/or electronic medical record (EMR)
- Willingness to be audio-recorded as per self-report
- Patient had their first visit with the clinician within the last 6 months
Caregiver Eligibility
- English speaking as per EMR
- Accompanying an MSK patient being seen by one of the consented HCPs as per the HCP and/or EMR
Exclusion Criteria:
- N/A
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GI/GU/Lymphoma Oncologists
Doctors specializing in treating gastrointestinal cancer (cancer of the stomach, pancreas, colon, etc.), genitourinary cancer (cancer of the genitals and urinary tract), and lymphoma (cancer affecting the blood and lymph nodes)
|
Health Care Professional's self-efficacy will be assessed by 12 ratings of self-reported confidence from (1) "strongly disagree" to (5) "strongly agree" in module-specific topics both before and after the training.
The UCLA Geriatrics Attitudes Scale is a 14-item scale developed to assess health care providers' attitudes toward older persons and caring for older patients.
Other Names:
The evaluation surveys for each of the three modules will contain fifteen statements assessing post-training attitudes regarding the skills learned and application of skills in oncology clinical practice, measured on a 5-point Likert scale.
|
|
Active Comparator: Participants with GI/GU/Lymphoma Cancer
Patients of the physicians in group 1
|
The Consultation and Relational Empathy (CARE) questionnaire is a 10-item self-report scale that measures a patient's satisfaction with how empathic their health care providers (HCP) was within a specific consultation.
Other Names:
Patients" perceptions of the quality of their interactions with their clinicians will be rated with 6 items from the Consumer Assessment of Health Care Providers and Systems Program (CAHPS)
Other Names:
The PAM scale contains 22 items that assess patient engagement in their care process.
Other Names:
|
|
Active Comparator: Caregivers of Participants with GI/GU/Lymphoma Cancer
Family members or caregivers of the patients in group 2
|
The Consultation and Relational Empathy (CARE) questionnaire is a 10-item self-report scale that measures a patient's satisfaction with how empathic their health care providers (HCP) was within a specific consultation.
Other Names:
Patients" perceptions of the quality of their interactions with their clinicians will be rated with 6 items from the Consumer Assessment of Health Care Providers and Systems Program (CAHPS)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of Health Care Provider (HCP) training
Time Frame: 8 weeks
|
Measured by number of HCP successfully recruited for the training
|
8 weeks
|
|
Participants satisfaction with Health Care Provider (HCP) training
Time Frame: 1 week
|
Self-reported measure of satisfaction
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Smita Banerjee, PhD, Memorial Sloan Kettering Cancer Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 7, 2018
Primary Completion (Actual)
February 16, 2024
Study Completion (Actual)
February 16, 2024
Study Registration Dates
First Submitted
May 8, 2018
First Submitted That Met QC Criteria
May 8, 2018
First Posted (Actual)
May 21, 2018
Study Record Updates
Last Update Posted (Actual)
February 20, 2024
Last Update Submitted That Met QC Criteria
February 19, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 18-183
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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