Evaluating an Alternative Clinical Genetics Cancer Care Delivery Model: A Pilot Study of Patient Outcomes

Sponsor
Memorial Sloan Kettering Cancer Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT02917798
Collaborator
United States Department of Defense (U.S. Fed)
1,022
5
85.7
204.4
2.4

Study Details

Study Description

Brief Summary

This study will evaluate patients' experiences with having gynecologic or prostate medical oncologists and surgeons offer them genetic testing, and having genetic counselors return the test results to patients over the telephone. This is different from the usual approach to genetic testing, where gynecologic or prostate medical oncologists and surgeons refer their patients to a genetic counselor in order to have these tests done, and the genetic counselors return the test results to the patient in person or over the telephone. The investigators will only be evaluating this alternative way of providing genetic testing to ovarian or prostate cancer patients.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Assessments

Study Design

Study Type:
Observational
Anticipated Enrollment :
1022 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluating an Alternative Clinical Genetics Cancer Care Delivery Model: A Pilot Study of Patient Outcomes
Actual Study Start Date :
Jul 12, 2016
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Genetic Testing in Ovarian ,Prostate or Pancreas Cancer

This study is a prospective single-arm study to examine how an alternative clinical genetics cancer care delivery model affects ovarian, prostate or pancreas cancer patients' cognitions, emotions, and behaviors. Participants will be contacted 1 week (+/- 1 week) (Assessment #2; and 3 months (+/- 2 weeks) (Assessment #3;) following the telephone post-test counseling session to complete the follow-up assessments. These assessments will measure psychological and behavioral study constructs.

Behavioral: Assessments

Outcome Measures

Primary Outcome Measures

  1. baseline to post-results change in distress levels [2 years]

    Change in distress levels (HADS-Anxiety) from Baseline to Assessments #2 and #3, measured as an effect size among participants who receive a pathogenic variant(s), no pathogenic variant(s), and variant(s) of uncertain significance

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • MSK patient age 18 years or older.

  • Diagnosed with or presumed by physician to have prostate cancer, or pancreatic cancer and recommended to undergo, currently undergoing, or having undergone active surveillance. (Patients with invasive epithelial ovarian cancer, peritoneal cancer, or fallopian tube cancer, or pancreas cancer are no longer eligible for inclusion as of Amendment 9. Patients with advanced prostate cancer who have not participated in active surveillance are no longer eligible for inclusion as of Amendment 10)

  • Deemed to be clinically appropriate for multiplex genetic testing by their physician.

  • Agreed to receive clinical multiplex genetic testing from their physician.

  • English-fluent; the surveys were designed and validated in English and are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures. Therefore, participants must be able to communicate in English to complete the surveys.

Exclusion Criteria:
  • Patients who do not or will not receive their ongoing cancer care at MSK.

  • Major psychiatric illness or cognitive impairment that in the judgment of the study investigators or study staff would preclude study participation.

  • Any patients who are unable to comply with the study procedures as determined by the study investigators or study staff.

  • For ovarian cancer patients only: patient insured by a payer that does not provide coverage for multiplex genetic testing as delivered in this protocol (e.g., Cigna, United Health Care, or Oxford, (because these payers require genetic counseling by a genetics professional prior to testing).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Memoral Sloan Kettering Basking Ridge Basking Ridge New Jersey United States
2 Memorial Sloan Kettering Commack Commack New York United States 11725
3 Memorial Sloan Kettering Westchester Harrison New York United States 10604
4 Memorial Sloan Kettering Cancer Center New York New York United States 10065
5 Memorial Sloan Kettering Rockville Centre Rockville Centre New York United States

Sponsors and Collaborators

  • Memorial Sloan Kettering Cancer Center
  • United States Department of Defense

Investigators

  • Principal Investigator: Maria Carlo, MD, Memorial Sloan Kettering Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Memorial Sloan Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT02917798
Other Study ID Numbers:
  • 16-919
First Posted:
Sep 28, 2016
Last Update Posted:
Feb 24, 2022
Last Verified:
Feb 1, 2022
Keywords provided by Memorial Sloan Kettering Cancer Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2022