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NCT07387263Recruiting

Mainstreaming Genetics: Evaluation of a Digital Application to Scale and Spread Oncologist-initiated Genetic Testing

Source: ClinicalTrials.gov · Last updated 30 Oct 2026

Brief summary (registry, in English)

Genetic testing can alter therapy and surgical management for cancer patients and is therefore indicated as a first-line test for many newly diagnosed patients, including breast, ovarian, pancreatic, prostate and colon/GI patients. To reduce pressure on already constrained genetics clinics across Canada, some cancer centres are 'mainstreaming' genetic testing - whereby genetic testing is initiated and mediated by oncologists without traditional pre-test genetic counseling (GC) often using some form of paper-based patient pamphlets or videos. There is no standard, evidence-based approach to mainstreaming, leading to significant practice variation, a lack of coordinated care and ultimately, negative psychological impacts on patients. Digital solutions can address these gaps by providing a standardized, coordinated and patient-centered approach to deliver cancer genetic education. However, digital solutions for providing cancer genetics services are uncommon and clinical-effectiveness and service delivery outcomes have not been well-assessed. This study will test a digital mainstreaming platform called the Genetics Adviser for Mainstream care to assess its effectiveness in improving psychological outcomes and patient-centred care for mainstream cancer patients compared to standard of care.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
180 (estimated)
First submitted
17 Dec 2025
Start date
30 Apr 2026
Primary completion date
31 Dec 2027
Lead sponsor
Unity Health Toronto
NCT number
NCT07387263

What you commit to

  • Study type: Interventional
  • Planned participants: 180
  • From 30 Apr 2026 to the primary completion date, 31 Dec 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receiving genetic testing information via a referral to a genetics clinic

Age

  • Under 18 years of age

Other

  • Do not speak or read English
  • Determined to have diminished, marginal and or fluctuating decisional capacity
  • Lack access to internet or an electronic device

Who the study is looking for

  • Receiving mainstream cancer germline testing related to primary cancer condition (ie. ovarian, pancreas, breast, prostate, or GI cancers) initiated by an oncologist.
  • 18 years old or older.
  • Speak and read English

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sunnybrook Hospital
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
Mount Sinai Hospital
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.