Efficacy of Written Versus Video Patient Education Materials for Postmastectomy Breast Reconstruction
Recruiting · NCT07602374 · Interventional (participants receive a specific treatment) · Lead sponsor: University of California, San Francisco
View the official record on ClinicalTrials.gov →Interventions studied
Medical Chart ReviewQuestionnairesVideo Health Education MaterialsWritten Health Education Materials
What this trial is about
This is a prospective, randomized controlled trial evaluating the comparative efficacy of written, video, and combined written and video patient education materials relative to no supplemental education for University of California, San Francisco (UCSF) patients presenting for post-mastectomy breast reconstruction consultation.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Adults aged 18 or older
- Presenting as a new patient to the UCSF plastic surgery breast reconstruction clinic
- Considering mastectomy, including:
- \- Therapeutic mastectomy in the setting of a breast cancer diagnosis
- \- Prophylactic mastectomy in the setting of a confirmed high-risk genetic variant
- \- Staged procedures, including delayed mastectomy with initial reduction
- Participants who are undecided between lumpectomy and mastectomy
Exclusion criteria
- Established patients returning for follow-up, in order to minimize confounding variables of individual surgeon education style on outcome measures
- Participants who are primarily considering lumpectomy or oncoplastic reduction at the time of their visit
- Non-English speakers, as educational materials are currently available in English only
Where it is running
1 location listed across 1 US state.
- University of California, San Francisco - San Francisco, California, United States