- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02823652
Pre-Test Genetic Education and Remote Genetic Counseling in Communicating Tumor Profiling Results to Patients With Advanced Cancer
COMET - Communication and Education in Tumor Profiling: A Randomized Study of Pre-Disclosure Genetic Education v. Usual Care in Tumor Profiling for Advanced Cancer and a Pilot Study of Remote Genetic Counseling for Participants With Potential Germline Mutations Identified on Tumor Profiling
Study Overview
Status
Detailed Description
PRIMARY OBJECTIVES:
I. To evaluate the efficacy of web-based pre-disclosure genetic education (i.e. before receipt of tumor profile results) to increase knowledge (genetic knowledge and knowledge of test benefits and limitations). (Step 1)
II. To evaluate the efficacy of web-based pre-disclosure genetic education (i.e. before receipt of tumor profile results) to decrease distress (anxiety, depression and cancer specific worry) compared to usual care services in patients undergoing tumor profiling for advanced cancer. (Step 1)
III. To evaluate the uptake of remote genetic counseling (Step 2)
IV. To evaluate the uptake of germline testing among advanced cancer patients with a potential clinically significant incidental germline mutation identified through tumor profiling in the Molecular Analysis for Therapy Choice (MATCH) trial. (Step 2)
SECONDARY OBJECTIVES:
I. To evaluate potential moderators suggested by the self-regulation theory of health behavior (SRTHB) (e.g. test result, sociodemographic factors, health literacy, baseline knowledge or distress) to changes in knowledge of genetic disease and test benefits and limitations. (Step 1)
II. To evaluate potential moderators suggested by the SRTHB (e.g test result, sociodemographic factors, health literacy, baseline knowledge or distress) to changes in distress in patients undergoing tumor profiling for advanced cancer. (Step 1)
III. To evaluate factors associated with uptake of genetic counseling and germline testing. (Step 2)
IV. To evaluate cognitive, affective and behavioral (communication to relatives) responses to confirmatory germline testing in advanced cancer patients with potential clinically significant incidental germline mutation identified in tumor profiling. (Step 2)
OUTLINE:
STEP I (PRIMARY INTERVENTION STUDY): Participants are randomized to 1 of 2 arms.
ARM A: Patients receive web-based genetic education consisting of general information about testing tumors for genetic mutations.
ARM B: Patients receive standard genetic education consisting of conversations with the treating physicians, interaction with and information from the clinical staff, and information from usual resources about testing for genetic mutations.
STEP II (SECONDARY GENETIC COUNSELING SUBSTUDY):
Patients who meet the criteria for the remote counseling substudy will receive genetic counseling over the telephone and undergo germline testing.
After completion of study treatment, patients are followed up periodically.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19103
- ECOG-ACRIN Cancer Research Group
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- (STEP 1) - PRIMARY INTERVENTION STUDY (RANDOMIZED CONTROLLED TRIAL [RCT]):
- Patients must be registered to the first screening step (Step 0) for the National Cancer Institute (NCI)-MATCH trial (EAY131)
- Patients must speak English and have an adequate ability to view a website (primary intervention study)
- (STEP 2) - SECONDARY GENETIC COUNSELING SUBSTUDY:
- Patients must have a potential germline mutation, as determined by the NCI-MATCH tumor profiling assay
- Patients must be able to speak English and hear by phone
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arm A (Step 1: internet-based intervention)
Patients receive web-based genetic education consisting of general information about testing tumors for genetic mutations.
|
Ancillary studies
Complete on-line genetic education
|
|
Active Comparator: Arm B (Step 1: usual care control)
Patients receive standard genetic education consisting of conversations with the treating physicians, interaction with and information from the clinical staff, and information from usual resources about testing for genetic mutations.
|
Ancillary studies
Undergo usual care
Other Names:
|
|
Experimental: Step 2 - genetic counseling
Patients who meet the criteria for the remote counseling substudy will receive genetic counseling over the telephone and undergo germline testing.
|
Ancillary studies
Complete remote counseling
Undergo germline testing
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of Scores on Cancer Genetic Knowledge Scale From Baseline to Post-genetic Education
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 14 items in the questionnaire of Cancer Genetic Knowledge Scale.
The total score ranges between 14 and 70.
Higher scores indicate more/better knowledge.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and compared between the two arms (arms A and B) at Step 1.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Patient-Reported Outcomes Measurement Information System (PROMIS) - Depression From Baseline to Post-genetic Education
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 4 items in the PROMIS - Depression questionnaire.
The total score ranges between 4 and 20.
Higher scores indicate more depression.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and compared between the two arms (arms A and B) at Step 1.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Patient-Reported Outcomes Measurement Information System (PROMIS) - Anxiety From Baseline to Post-genetic Education
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 4 items in the PROMIS - Anxiety questionnaire.
The total score ranges between 4 and 20.
Higher scores indicate more anxiety.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and compared between the two arms (arms A and B) at Step 1.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Impact of Events Scale (IES) From Baseline to Post-genetic Education
Time Frame: Assessed at baseline and up to 14 days post-baseline
|
There are 14 items in the questionnaire of Impact of Events Scale (IES).
The total score ranges between 0 and 70.
Higher scores indicate more stress.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and compared between the two arms (arms A and B) at Step 1.
|
Assessed at baseline and up to 14 days post-baseline
|
|
Proportion of Participants Who Complete Remote Genetic Counseling in the Genetic Counseling Substudy (Step 2)
Time Frame: Assessed at baseline at Step 2
|
Among participants who registered in the genetic counseling substudy (Step 2), the proportion of participants who completed remote genetic counseling will be reported.
The proportion is defined as "the number of participants who completed remote genetic counseling divided by the number of participants who agreed to participate in the genetic counseling study".
|
Assessed at baseline at Step 2
|
|
Proportion of Participants Who Complete Germline Testing in the Genetic Counseling Substudy (Step 2)
Time Frame: Assessed at baseline at Step 2
|
Among participants who registered in the genetic counseling substudy (Step 2), the proportion of participants who completed remote genetic counseling will be reported.
The proportion is defined as "the number of participants who completed remote genetic counseling divided by the number of participants who agreed to participate in the genetic counseling study".
|
Assessed at baseline at Step 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of Scores on Cancer Genetic Knowledge Scale From Baseline to Post-genetic Education by Arm and Sex
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 14 items in the questionnaire of Cancer Genetic Knowledge Scale.
The total score ranges between 14 and 70.
Higher scores indicate more/better knowledge.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and interaction between arm and sex was evaluated.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Patient-Reported Outcomes Measurement Information System (PROMIS) - Depression From Baseline to Post-genetic Education by Arm and Sex
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 4 items in the PROMIS - Depression questionnaire.
The total score ranges between 4 and 20.
Higher scores indicate more depression.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and interaction between arm and sex was evaluated.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Patient-Reported Outcomes Measurement Information System (PROMIS) - Anxiety From Baseline to Post-genetic Education by Arm and Sex
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 4 items in the PROMIS - Anxiety questionnaire.
The total score ranges between 4 and 20.
Higher scores indicate more anxiety.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and interaction between arm and sex was evaluated.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
|
Change of Scores on Impact of Events Scale (IES) From Baseline to Post-genetic Education by Arm and Sex
Time Frame: Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
There are 14 items in the questionnaire of Impact of Events Scale (IES).
The total score ranges between 0 and 70.
Higher scores indicate more stress.
The questionnaire was administered at baseline and post-genetic education.
The change of scores from baseline to post-genetic education were calculated and interaction between arm and sex was evaluated.
|
Assessed at baseline and post-genetic education (about 1-2 weeks post-baseline)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Factors Associated With Uptake of Remote Genetic Counseling in the Genetic Counseling Substudy (Step 2)
Time Frame: Assessed at baseline in Step 2
|
The associations between patient characteristics and whether a patient receives genetic counseling will be evaluated.
|
Assessed at baseline in Step 2
|
|
Cognitive and Affective Responses to Confirmatory Germline Testing (Step 2)
Time Frame: Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
Cognitive and affective responses to confirmatory germline testing in advanced cancer patients with potential clinically significant incidental germline mutation identified in tumor profiling will be evaluated.
|
Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
|
Satisfaction and Regret/Disappointment Related to Tumor Genetic Test Results
Time Frame: Assessed within 3 days of tumor test results received
|
Satisfaction and regret/disappointment related to tumor genetic test results will be evaluated.
|
Assessed within 3 days of tumor test results received
|
|
How to Better Deliver Tumor Genetic Test Results and Germline Information in the Future
Time Frame: Assessed at baseline, within 3 days of genetic test results received, within 3 days of germline testing results received
|
How to better deliver tumor genetic test results and germline information in the future will be evaluated.
|
Assessed at baseline, within 3 days of genetic test results received, within 3 days of germline testing results received
|
|
Behavioral Responses to Confirmatory Germline Testing
Time Frame: Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
Behavioral responses (communication to others) to confirmatory germline testing in advanced cancer patients with potential clinically significant incidental germline mutation identified in tumor profiling will be evaluated.
|
Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
|
Satisfaction and Regret/Disappointment Related to Genetic Counseling Service or Germline Genetic Test Results
Time Frame: Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
Satisfaction and regret/disappointment related to genetic counseling service or germline genetic test results will be evaluated
|
Assessed at baseline, within 3 days of remote genetic counseling, within 3 days of germline testing results received, and 3 months after germline testing results received in Step 2
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Angela Bradbury, ECOG-ACRIN Cancer Research Group
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EAQ152 (Other Identifier: CTEP)
- NCI-2015-02253 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Advanced Malignant Neoplasm
-
University of California, San FranciscoCompletedIntegrative Palliative Care/Psycho-Oncology Telehealth Intervention in Patients With Advanced CancerAdvanced Malignant Solid Neoplasm | Locally Advanced Malignant Solid Neoplasm | Metastatic Malignant Solid NeoplasmUnited States
-
Wake Forest University Health SciencesNational Cancer Institute (NCI)CompletedMetastatic Malignant Neoplasm | Unresectable Malignant Neoplasm | Advanced Malignant NeoplasmUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)Active, not recruitingMalignant Neoplasm | Metastatic Malignant Neoplasm | Advanced Malignant Neoplasm | Recurrent Malignant Neoplasm | Locally Advanced Malignant NeoplasmUnited States
-
M.D. Anderson Cancer CenterTerminatedLocally Advanced Malignant Solid Neoplasm | Unresectable Malignant Solid Neoplasm | Metastatic Malignant Solid NeoplasmUnited States
-
National Cancer Institute (NCI)CompletedAdvanced Malignant Solid Neoplasm | Unresectable Malignant Solid Neoplasm | Metastatic Malignant Solid NeoplasmUnited States
-
University of Southern CaliforniaNational Cancer Institute (NCI)Active, not recruitingAdvanced Malignant Solid Neoplasm | Refractory Malignant Solid NeoplasmUnited States
-
National Cancer Institute (NCI)CompletedAdvanced Malignant Solid Neoplasm | Refractory Malignant Solid NeoplasmUnited States
-
M.D. Anderson Cancer CenterCompletedAdvanced Malignant Solid Neoplasm | Refractory Malignant Solid NeoplasmUnited States
-
Mayo ClinicNational Cancer Institute (NCI)CompletedAdvanced Malignant Solid Neoplasm | Metastatic Malignant Solid NeoplasmUnited States
-
National Cancer Institute (NCI)Active, not recruitingAdvanced Rare Malignant Solid Neoplasm | Rare Malignant Solid Neoplasm | Refractory Rare Malignant Solid NeoplasmUnited States
Clinical Trials on Survey Administration
-
Centre Oscar LambretCentre Hospitalier Universitaire de BesanconTerminated
-
Rutgers, The State University of New JerseyNational Cancer Institute (NCI)TerminatedHealth Status UnknownUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)CompletedSarcoma | Breast Carcinoma | Head and Neck CarcinomaUnited States
-
Boston UniversityNational Heart, Lung, and Blood Institute (NHLBI)Completed
-
M.D. Anderson Cancer CenterRecruitingHematopoietic and Lymphoid Cell Neoplasm | Malignant Solid Neoplasm | COVID-19 InfectionUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)RecruitingMalignant Vascular NeoplasmUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)RecruitingMelanoma | COVID-19 InfectionUnited States
-
ECOG-ACRIN Cancer Research GroupNational Cancer Institute (NCI)WithdrawnMelanoma | Breast Carcinoma | Lung Carcinoma | Colorectal Carcinoma | Community Practice | Solid NeoplasmUnited States
-
M.D. Anderson Cancer CenterNational Institutes of Health (NIH)Active, not recruitingHematopoietic and Lymphoid Cell Neoplasm | Malignant Solid NeoplasmUnited States
-
University of Rochester NCORP Research BaseNational Cancer Institute (NCI)WithdrawnCommunity Practice | StaffUnited States