Skip to main content
Clinical Trials/NCT04508764
NCT04508764TerminatedNot Applicable

Implementation of the Families Accelerating Cascade Testing Toolkit (FACTT) for Hereditary Breast and Ovarian Cancer and Lynch Syndrome

Washington University School of Medicine1 site in 1 country96 target enrollmentStarted: April 9, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
96
Locations
1
Primary Endpoint
Proband-reported cascade testing rates of first-degree relatives

Study Overview

Brief Summary

The purpose of this research study is to learn how cancer care providers can help their patients communicate the need for genetic testing in families with inherited cancer syndromes.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Documentation of HBOC or Lynch-associated "pathogenic/ likely pathogenic" mutation per American College of Medical Genetics and Genomics criteria (1)
  • •Diagnosis of one or more invasive cancers: epithelial ovarian, fallopian tube, primary peritoneal, breast, colorectal, endometrial
  • •Mutation listed in NCCN guidelines with at least Category 2A evidence for intervention
  • •Over the age of 18
  • •Psychological ability and general health that permits completion of study requirements and follow-up
  • •Willingness to complete follow-up surveys in person, electronically, or by telephone for up to 6 months

Exclusion Criteria

  • •"Variant of undetermined significance," "likely benign" or "benign" variant per ACMGG criteria

Arms & Interventions

Usual Care

No Intervention
  • For approximately the first 6 months of the study, or until 75 patient with cancer who is initially approached in clinic (probands) are enrolled, the investigators will be enrolling probands into the "Usual Care" group. During this time, the investigators will clarify usual care regarding cascade genetic testing for each participating clinic and proband participant. The investigators will do this by proband participant surveys, as well as initial provider semi-structured interviews.
  • Proband: Complete Cascade Genetic Testing survey. The survey will also contain questions regarding willingness or not to invite each eligible 1st degree family member to participate in the family study. At 6 months, there will be a follow-up survey
  • Family Member: Complete survey at study entry and at 6 month follow-up

FACT Toolkit (FACTT)

Experimental
  • Proband: Introduced to FACTT and will complete Cascade Genetic Testing survey. The survey will contain questions regarding willingness or not to invite each eligible 1st degree family member to participate in the family study. The probands will also fill out assessments of each FACTT component. At 6 months, there will be a follow-up survey.
  • Family Member: Introduced to FACTT and will complete surveys at study entry and 6 month follow-up. They will also fill out assessments of each FACTT component

Intervention: Families Accelerating Cascade Testing Toolkit (Other)

Outcomes

Primary Outcomes

Proband-reported cascade testing rates of first-degree relatives

Time Frame: From start of study through completion of 6 month follow-up (estimated to be 18 months)

-For each proband, this testing rate is defined as the number of first-degree relatives tested divided by the number of living first-degree relatives age-appropriate for testing, as determined by family surveys done by the proband. The investigators will calculate mean cascade genetic testing rates for both conditions (Usual Care and FACTT intervention).

Family member-reported cascade testing rates

Time Frame: From start of study through completion of 6 month follow-up (estimated to be 18 months)

-This testing rate is defined by the number of family members tested divided by the number of living family members age-appropriate for testing

Number of primary barriers to genetic testing for family members

Time Frame: From start of study through completion of 6 month follow-up (estimated to be 18 months)

-The Family Member survey will assess experience with considering testing themselves, decisional regret regarding genetic testing, and if they have tested positive

Number of primary barriers to genetic testing for first-degree relatives

Time Frame: From start of study through completion of 6 month follow-up (estimated to be 18 months)

-The Cascade Genetic Testing survey will assess knowledge, perception, and personal experience with sharing germline mutation information with first-degree relatives

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials