Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07602374 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
100
Enrollment target

NCT07602374: Recruiting NA study, sponsored by University of California, San Francisco.

NCT07602374 is a NA study that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07602374, a NA study, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
100 participants
Enrollment target

Study 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.

Primary Outcome

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

Interventions

  • OTHER Medical Chart Review
  • OTHER Questionnaires
  • OTHER Video Health Education Materials
  • OTHER Written Health Education Materials

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-06-06
Est. Completion 2029-03-31
Phase NA

What NCT07602374 shows while recruiting

NCT07602374 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 4 interventions - of which Medical Chart Review is the first listed.

NCT07602374 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07602374 about?

NCT07602374 is a clinical study titled "Efficacy of Written Versus Video Patient Education Materials for Postmastectomy Breast Reconstruction". 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...

What is the current status of trial NCT07602374?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2026-06-06. Estimated completion is 2029-03-31.

What interventions are being tested in trial NCT07602374?

The interventions under investigation include: Medical Chart Review (OTHER), Questionnaires (OTHER), Video Health Education Materials (OTHER), Written Health Education Materials (OTHER).

Who is sponsoring clinical trial NCT07602374?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07602374's enrollment target sits among peer trials

100 840th of 2000 higher than 1,081 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07602374, the US trial registry maintained by the National Library of Medicine. NCT07602374 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.