Efficacy of Written Versus Video Patient Education Materials for Postmastectomy Breast Reconstruction

NCT07602374 — Not applicable, Recruiting, 100 participants, University of California, San Francisco

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Evaluating the Efficacy of Written Versus Video Patient Education Materials for Postmastectomy Breast Reconstruction Patients: Knowledge, Confidence, and Anxiety

RegistryNCT07602374
StatusRecruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, supportive care
Enrollment100 (Estimated)
SponsorUniversity of California, San Francisco (Other)
ConditionsBreast Surgery
InterventionsQuestionnaires, Video Health Education Materials, Written Health Education Materials, Medical Chart Review (Other)
Datesstart 2026-06-06, primary completion 2028-03-31 (estimated), completion 2029-03-31 (estimated), first posted 2026-05-22, last updated 2026-06-12
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Breast Surgery All trials of Questionnaires All trials of Video Health Education Materials

-Summary

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.

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+Detailed description

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

+Arms and interventions

ArmTypeInterventionsDescription
Written Educational InterventionExperimentalOther: Questionnaires; Other: Written Health Education Materials; Other: Medical Chart ReviewOn 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 InterventionExperimentalOther: Questionnaires; Other: Video Health Education Materials; Other: Medical Chart ReviewOn 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 InterventionExperimentalOther: Questionnaires; Other: Video Health Education Materials; Other: Written Health Education Materials; Other: Medical Chart ReviewOn 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 ArmOtherOther: Questionnaires; Other: Medical Chart ReviewOn 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.
  • Questionnaires (Other), also known as Surveys: Participants will complete health related questionnaires.
  • Video Health Education Materials (Other), also known as Health Education Materials: Five-module video series
  • Written Health Education Materials (Other), also known as Health Education Materials: 20-page illustrated brochure
  • Medical Chart Review (Other), also known as Chart Review: Participants may have data collected from the medical record.

+Outcome measures

Primary outcomes

  • Mean scores on the Spielberger State-Trait Anxiety Inventory (STAI), State Form [1 day, during appointment immediately prior to meeting with surgeon]: STAI is a 20 items instrument for assessing trait anxiety and 20 for state anxiety for a total of 40 items. State anxiety items include: "I am tense; I am worried" and "I feel calm; I feel secure." Trait anxiety items include: "I worry too much over something that really doesn't matter" and "I am content; I am a steady person." All items are rated on a 4-point scale (e.g., from "1=Almost Never" to 4="Almost Always") with a maximum score range of 40-160 when all 40 items are administered. Higher scores indicate greater anxiety. Participants will complete STAI at baseline and during clinic visit with surgeon. Means, standard deviation, and group differences of the scores with confidence intervals will be reported.
  • Mean scores on the Preparation for Decision Making (PrepDM) Scale - [1 day, during appointment immediately prior to meeting with surgeon]: The PrepDM is a validated 10-item tool that assesses a patient's perception of how well a decision aid or intervention, such as a decision aid, educational material, or clinical consultation, helps a patient feel prepared to make a health decision and discuss it with their practitioner. It evaluates a patient's perceived readiness across several aspects of decision-making, including understanding available options, recognizing benefits and risks, clarifying personal values, and feeling confident about communicating with healthcare providers. It uses a 5-point Likert scale (1=Not at all, 5=A great deal), with higher score reflecting greater perceived preparation for decision-making. Participants will complete PrepDM at baseline and during clinic visit with surgeon. Means, standard deviation, and group differences of the scores with confidence intervals will be reported.
  • Mean scores on Reconstruction-Specific Knowledge Quiz [1 day, during appointment immediately prior to meeting with surgeon]: Reconstruction-specific knowledge quiz is a 7-item quiz. It is an author-developed instrument assessing knowledge of the reconstructive options covered in the educational materials, including implant-based reconstruction, autologous reconstruction, Goldilocks reconstruction, and the option of going flat. Participants will complete Reconstruction-Specific Knowledge Quiz at baseline and during clinic visit with surgeon. Means, standard deviation, and group differences of the scores with confidence intervals will be reported.

+Eligibility

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

+Locations (1)

FacilityCityCountryStatus
University of California, San FranciscoSan Francisco, CaliforniaUnited StatesRecruiting

+Investigators

  • Merisa Piper, MD, Principal investigator, University of California, San Francisco