Evaluating the Efficacy of Written Versus Video Patient Education Materials for Postmastectomy Breast Reconstruction Patients: Knowledge, Confidence, and Anxiety
| Registry | NCT07602374 |
|---|---|
| Status | Recruiting |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: none, supportive care |
| Enrollment | 100 (Estimated) |
| Sponsor | University of California, San Francisco (Other) |
| Conditions | Breast Surgery |
| Interventions | Questionnaires, Video Health Education Materials, Written Health Education Materials, Medical Chart Review (Other) |
| Dates | start 2026-06-06, primary completion 2028-03-31 (estimated), completion 2029-03-31 (estimated), first posted 2026-05-22, last updated 2026-06-12 |
| Locations | 1 site in United States |
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All trials for Breast Surgery All trials of Questionnaires All trials of Video Health Education Materials
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.
PRIMARY OBJECTIVES:
1. Assess baseline knowledge, procedural confidence, and anxiety in patients presenting for breast reconstruction consultation.
2. Compare post-intervention outcomes between patients receiving written, video, or combined educational materials relative to no supplemental education.
SECONDARY OBJECTIVES
1\. Examine whether the relative efficacy of each modality differs across patient subgroups defined by age, area deprivation index score, and prior health literacy.
OUTLINE:
Participants will be randomized into 1 of 4 groups:
1. Written educational intervention
2. Video educational intervention
3. Combined written and video educational intervention
4. No additional educational intervention
Outcome measures are assessed at a single timepoint following participant review of assigned materials and prior to the clinical consultation. Enrolled participants who do not review their assigned educational materials prior to the clinical consultation will be excluded from primary analysis but will be included in secondary intent-to-treat analysis
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Written Educational Intervention | Experimental | Other: Questionnaires; Other: Written Health Education Materials; Other: Medical Chart Review | On the day of consultation prior to meeting with the plastic surgeon, participants will receive a 20-page illustrated brochure covering the full range of reconstructive options and be asked to complete surveys. Following the appointment, a medical chart review will be conducted. |
| Video Educational Intervention | Experimental | Other: Questionnaires; Other: Video Health Education Materials; Other: Medical Chart Review | On the day of consultation prior to meeting with the plastic surgeon, participants will receive a five-module video series totaling approximately 20 minutes featuring the senior author and will be asked to complete surveys; expected to take no longer than 10 minutes to complete. Following the appointment, a medical chart review will be conducted. |
| Combined Educational Intervention | Experimental | Other: Questionnaires; Other: Video Health Education Materials; Other: Written Health Education Materials; Other: Medical Chart Review | On the day of consultation prior to meeting with the plastic surgeon, participants in the combined arm will receive both written and video materials and will be asked to complete surveys. Following the appointment, a medical chart review will be conducted. |
| No Supplemental Education / Control Arm | Other | Other: Questionnaires; Other: Medical Chart Review | On the day of consultation prior to meeting with the plastic surgeon, participants will be asked to complete surveys. Following the appointment, a medical chart review will be conducted. |
Sex: All, ages: 18 Years to any
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
| Facility | City | Country | Status |
|---|---|---|---|
| University of California, San Francisco | San Francisco, California | United States | Recruiting |