Protocol - Clinician Confidence in Returning Genetic Test Results
Description
The healthcare provider is asked about his or her knowledge of genetic results without seeking information from other sources. A scale with responses from “not at all confident” to “very confident” is used to measure the provider’s confidence. A second set of items refers to the usefulness of the genetic test results with a scale that ranges from strongly disagree to strongly agree.
Specific Instructions
The following instructions appear at the top of the Clinical Sequencing Evidence-Generating Research Consortium (CSER) questionnaire.
Timeframe: within 0–6 weeks of Return of Results (RoR) visit.
Audience: Providers of participants receiving all types of results (positive, negative, variance of unknown sequence [VUS], secondary). Necessary to include providers receiving positive results, VUS results, and secondary results. Number of providers receiving negative results should be at least equal to the number of positive results—or more, if budget and time allow.
Target: The provider who will be primarily responsible for managing the results and making medical recommendations, the patient’s current medical home for the reason the testing was performed. This may or may not be the same provider that disclosed the results as part of the study. It could be a primary or specialty care provider.
Availability
Protocol
Have you had a medical encounter with your patient since you received the genomic result?
[ ] Yes
[ ] No
1. Before looking at resources other than those provided with the result, when you received the genomic result, how confident did you feel in your…
Knowledge about the condition caused by this gene?
[ ] Not at all confident
[ ] A little confident
[ ] Somewhat confident
[ ] Very confident
Ability to explain the result to your patient?
[ ] Not at all confident
[ ] A little confident
[ ] Somewhat confident
[ ] Very confident
Ability to answer your patient’s questions about the results?
[ ] Not at all confident
[ ] A little confident
[ ] Somewhat confident
[ ] Very confident
Ability to personally manage the patient’s care based on the result?
[ ] Not at all confident
[ ] A little confident
[ ] Somewhat confident
[ ] Very confident
2. To what extent do you agree with the following statements about receiving this unsolicited genomic result?
The result was informative
[ ] Strongly disagree
[ ] Somewhat disagree
[ ] Somewhat agree
[ ] Strongly agree
The result was confusing
[ ] Strongly disagree
[ ] Somewhat disagree
[ ] Somewhat agree
[ ] Strongly agree
The result was helpful
[ ] Strongly disagree
[ ] Somewhat disagree
[ ] Somewhat agree
[ ] Strongly agree
The result was useless
[ ] Strongly disagree
[ ] Somewhat disagree
[ ] Somewhat agree
[ ] Strongly agree
Personnel and Training Required
The interviewer must be trained to conduct personal interviews with individuals from the general population. The interviewer must be trained and found to be competent (i.e., tested by an expert) at the completion of personal interviews. The interviewer should be trained to prompt respondents further if a “don’t know” response is provided.
Note: Also administered as an online questionnaire.
Equipment Needs
The PhenX Working Group acknowledges these questions can be administered in a computerized or noncomputerized format (i.e., paper-and-pencil instrument). Computer software is necessary to develop computer-assisted instruments. The interviewer will require a laptop computer/handheld computer to administer a computer-assisted questionnaire.
Requirements
Requirement Category | Required |
---|---|
Major equipment | No |
Specialized training | No |
Specialized requirements for biospecimen collection | No |
Average time of greater than 15 minutes in an unaffected individual | No |
Mode of Administration
Self-administered or interviewer-administered questionnaire
Lifestage
Infant, Toddler, Child, Adolescent, Adult, Senior, Pregnancy
Participants
Healthcare providers after sharing the genetic results with the patient.
Selection Rationale
These items are from a questionnaire recommended by a consortium of genomic experts and they are low burden.
Language
English
Standards
Standard | Name | ID | Source |
---|
Derived Variables
None
Process and Review
Not applicable
Protocol Name from Source
Clinical Sequencing Evidence-Generating Research Consortium (CSER) Provider Measures - Post-Return of Results Follow-up #1 & Electronic Medical Records and Genomics (eMERGE) Post-Return of Results Provider Follow-up Questionnaire
Source
Clinical Sequencing Evidence-Generating Research Consortium (CSER) Provider Measures – Post-Return of Results Follow-up #1
Electronic Medical Records and Genomics (eMERGE) Post–Return of Results Provider Follow-up Questionnaire
General References
Manuscripts are in progress.
Protocol ID
310501
Variables
Export VariablesVariable Name | Variable ID | Variable Description | dbGaP Mapping | |
---|---|---|---|---|
PX310501_Clinician_Confidence_Ability_Explain_Genetic_Results | ||||
PX310501020200 | Before looking at resources other than those more | N/A | ||
PX310501_Clinician_Confidence_Answer_Questions_Genetic_Results | ||||
PX310501020300 | Before looking at resources other than those more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Confusing | ||||
PX310501030200 | To what extent do you agree with the more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Encounter_Patient_After | ||||
PX310501010000 | Have you had a medical encounter with your more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Helpful | ||||
PX310501030300 | To what extent do you agree with the more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Informative | ||||
PX310501030100 | To what extent do you agree with the more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Knowledge_Condition | ||||
PX310501020100 | Before looking at resources other than those more | N/A | ||
PX310501_Clinician_Confidence_Genetic_Results_Useless | ||||
PX310501030400 | To what extent do you agree with the more | N/A | ||
PX310501_Clinician_Confidence_Manage_Patient_Care_Genetic_Results | ||||
PX310501020400 | Before looking at resources other than those more | N/A |
Measure Name
Clinician Confidence in Returning Genetic Test Results
Release Date
September 10, 2020
Definition
A series of questions to assess a healthcare provider’s knowledge and understanding of the genetic test results and the usefulness of the results related to the care of a patient.
Purpose
To assess healthcare providers’ understanding of genetic test results and the health and care implications for each patient.
Keywords
Test results, genetic testing, genomic medicine, Clinical Sequencing Evidence-Generating Research Consortium, CSER, Electronic Medical Records and Genomics, eMERGE, return of results, RoR, provider
Measure Protocols
Protocol ID | Protocol Name |
---|---|
310501 | Clinician Confidence in Returning Genetic Test Results |
Publications
There are no publications listed for this protocol.