[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT05772130":3,"trial-entities:NCT05772130":111,"trial-summary:NCT05772130":116},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":22,"study_type":23,"primary_purpose":24,"phases":25,"enrollment_info":27,"interventions":30,"primary_outcomes":54,"secondary_outcomes":59,"sex":60,"minimum_age":61,"maximum_age":62,"healthy_volunteers":15,"eligibility_criteria":63,"std_ages":85,"locations":88,"central_contacts":105,"overall_officials":106,"references":109,"see_also_links":110},"NCT05772130","22261","Provider-Mediated Communication of Genetic Testing Results to At-Risk Relatives of Cancer Patients to Improve Genetic Counseling and Testing Rates, Family HOPE Study","Family HOPE Study (Hereditary Lynch Syndrome Opportunities for Participation &Amp; Engagement)","RECRUITING","2026-12-21","2025-12","2026-01-05","2023-02-14","City of Hope Medical Center","OTHER",true,"This clinical trial tests whether provider-mediated communication of genetic testing results to at-risk relatives of cancer patients can help improve genetic counseling and testing rates. Approximately 15% of people with cancer have an inherited form of cancer due to changes in a gene that they have inherited from one of their parents. These changes increase a person's risk for developing cancer. Most people who have an inherited harmful change in a cancer risk gene don't know that they have it and are therefore not able to get the health care that they need. The primary reason for this problem has been a lack of genetic counseling and testing for cancer patients and patients with a strong family history of cancer. Another reason for this lack of awareness is that, when cancer runs in a family, the patient who carries the gene change usually has to communicate the genetic risk information to their family members. When this process doesn't work well, family members may not know that they need to get genetic testing and then may not get potentially life-saving care. Provider-mediated contact to discuss genetic test results may help improve rates of genetic testing among at-risk relatives of patients with a family cancer syndrome.","PRIMARY OBJECTIVES:\n\nI. Improve rates of family member cascade testing. II. Evaluate the psychosocial impact of provider-mediated contact to communicate genetic testing results.\n\nOUTLINE: Participants are randomized to 1 of 2 arms.\n\nARM I: Patients receive a family letter and their genomic test report to share with at-risk first degree relatives on study.\n\nARM II: Patients receive a family letter and their genomic test report to share with at-risk first degree relatives and relatives also receive provider-mediated contact to discuss genetic results on study.",[19,20,21],"Hematopoietic and Lymphoid System Neoplasm","Hereditary Malignant Neoplasm","Malignant Solid Neoplasm",[],"INTERVENTIONAL","HEALTH_SERVICES_RESEARCH",[26],"NA",{"count":28,"type":29},240,"ESTIMATED",[31,39,44,51],{"type":14,"name":32,"description":33,"armGroupLabels":34,"otherNames":36},"Best Practice","Receive family letter and genomic test report",[35],"Arm I (usual care)",[37,38],"standard of care","standard therapy",{"type":14,"name":40,"description":41,"armGroupLabels":42},"Electronic Health Record Review","Ancillary studies",[35,43],"Arm II (provider-mediated contact)",{"type":45,"name":46,"description":47,"armGroupLabels":48,"otherNames":49},"BEHAVIORAL","Personal Contact","Receive family letter and genomic test report with provider-mediated contact",[43],[50],"Contact",{"type":14,"name":52,"description":41,"armGroupLabels":53},"Survey Administration",[35,43],[55],{"measure":56,"description":57,"timeFrame":58},"The percentage of uptake of cascade testing among patients' first-degree at-risk relatives","Will calculate descriptive statistics first, including the mean, median and standard deviation of the number of the first-degree and secondary-degree at-risk relatives. We will then compare the proportion of identified relatives who completed genetic testing between the intervention and the control arms with a one-sided Cochran-Mantel-Haenszel test. Type I error of 0.05 will be used and descriptive statistics will be calculated for all exploratory outcomes along with 95% confidence intervals. All statistical testing and calculation of confidence intervals will adjust for intra-proband correlation.","Up to 9 months after enrollment",[],"ALL","18 Years",null,{"inclusion":64,"exclusion":77,"raw_text":84},[65,66,67,68,69,70,71,72,73,74,75,76],"PATIENTS: Enrolled in City of Hope (COH) institutional review board (IRB) 07047 or have been seen by COH Genetics for genetic testing","PATIENTS: Have an pathogenic\u002F likely pathogenic germline variant","PATIENTS: Fluent in English","PATIENTS: Age \\>= 18 years","PATIENTS: Willing to provide contact information for eligible first-degree relatives","PATIENTS: \\>= 2 first-degree relatives that are eligible for genetic testing and reside in the United States of America","FIRST-DEGREE RELATIVES: Proband is a COH patient and has consented to this study","FIRST-DEGREE RELATIVES: First-degree relative of proband","FIRST-DEGREE RELATIVES: Resides within the United States","FIRST-DEGREE RELATIVES: Has not undergone genetic testing for the known familial variant","FIRST-DEGREE RELATIVES: Are fluent in English","FIRST-DEGREE RELATIVES: Age \\>= 18 years",[78,79,80,81,82,83],"PATIENTS: Unable to provide informed consent","PATIENTS: =\\\u003C 2 at-risk first-degree relatives who are eligible for genetic testing and\u002For reside within the United States","PATIENTS: Unwilling to provide contact information for family members","FIRST-DEGREE RELATIVES: Unable or unwilling to provide informed consent","FIRST-DEGREE RELATIVES: Have undergone genetic testing for the known familial variant","FIRST-DEGREE RELATIVES: Resides outside of the United States","Inclusion Criteria:\n\n* PATIENTS: Enrolled in City of Hope (COH) institutional review board (IRB) 07047 or have been seen by COH Genetics for genetic testing\n* PATIENTS: Have an pathogenic\u002F likely pathogenic germline variant\n* PATIENTS: Fluent in English\n* PATIENTS: Age \\>= 18 years\n* PATIENTS: Willing to provide contact information for eligible first-degree relatives\n* PATIENTS: \\>= 2 first-degree relatives that are eligible for genetic testing and reside in the United States of America\n* FIRST-DEGREE RELATIVES: Proband is a COH patient and has consented to this study\n* FIRST-DEGREE RELATIVES: First-degree relative of proband\n* FIRST-DEGREE RELATIVES: Resides within the United States\n* FIRST-DEGREE RELATIVES: Has not undergone genetic testing for the known familial variant\n* FIRST-DEGREE RELATIVES: Are fluent in English\n* FIRST-DEGREE RELATIVES: Age \\>= 18 years\n\nExclusion Criteria:\n\n* PATIENTS: Unable to provide informed consent\n* PATIENTS: =\\\u003C 2 at-risk first-degree relatives who are eligible for genetic testing and\u002For reside within the United States\n* PATIENTS: Unwilling to provide contact information for family members\n* FIRST-DEGREE RELATIVES: Unable or unwilling to provide informed consent\n* FIRST-DEGREE RELATIVES: Have undergone genetic testing for the known familial variant\n* FIRST-DEGREE RELATIVES: Resides outside of the United States",[86,87],"ADULT","OLDER_ADULT",[89],{"facility":13,"status":8,"city":90,"state":91,"zip":92,"country":93,"contacts":94,"geoPoint":102},"Duarte","California","91010","United States",[95,100],{"name":96,"role":97,"phone":98,"email":99},"Stacy W. Gray","CONTACT","626-218-8662","stagray@coh.org",{"name":96,"role":101},"PRINCIPAL_INVESTIGATOR",{"lat":103,"lon":104},34.13945,-117.97729,[],[107],{"name":108,"affiliation":13,"role":101},"Stacy W Gray",[],[],{"nct_id":4,"conditions":112,"biomarkers":114},[113,20,21],"Hematopoietic and Lymphatic System Neoplasm",[115],"Germline Variation",{"nct_id":4,"found":15,"summary":117,"prompt_version":127},{"design":118,"status":119,"heading":120,"summary":121,"follow_up":122,"word_count":123,"commitments":124,"compensation":125,"drugs_mentioned":126},"This is an interventional study with 240 participants. Participants will be randomly assigned to one of two groups.","completed","Family HOPE Study: Improving Genetic Testing for Cancer Risk","This study, called the Family HOPE Study, is looking at better ways to share genetic test results with family members who might also be at risk for cancer. About 15% of cancers are inherited, meaning they run in families due to changes in certain genes. Many people don't know they have these gene changes, which can prevent them from getting important healthcare. This study wants to see if having a healthcare provider help communicate these genetic results to at-risk relatives can increase the number of people who get genetic counseling and testing. You might be able to join if you are an adult cancer patient treated at City of Hope, have a specific gene change linked to cancer, and are willing to share contact information for your first-degree relatives (like parents, siblings, or children). The study will measure how many of your relatives get tested within 9 months.","The primary endpoint is measured up to 9 months after enrollment.",148,"Not specified in the trial record.","Not stated in the trial record.",[],"v2"]