WashU DIEP Flap Video and Patient Understanding Improvement
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: Questionnaires
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Patients will complete a survey before and after watching the WashU DIEP Flap Video at their pre-operative standard of care visit, and a third survey at their post-operative standard of care visit."
- "These surveys will use questions from SILS, APAIS, PEMAT, and AIM/IAM to assess the patient's health literacy, demographics questions, and questions concerning patient understanding and anxiety surrounding the procedure."
- "The purpose of the post-op survey will be to assess how well the video set expectations of the procedure and recovery process and will repeat questions asked pre-operatively."
- "Primary Objective: The primary aim of the study is to determine if our animated video affects understanding and anxiety survey scores in patients undergoing DIEP breast reconstruction."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests whether an animated video helps patients understand DIEP-flap breast reconstruction and feel less worried about it. This surgery uses tissue from the belly to rebuild a breast. Adults scheduled for this surgery at Barnes Jewish Hospital will take surveys before and after watching the video, and again after surgery.
Patients will complete a survey before and after watching the WashU DIEP Flap Video at their pre-operative standard of care visit, and a third survey at their post-operative standard of care visit. These surveys will use questions from SILS, APAIS, PEMAT, and AIM/IAM to assess the patient's health literacy, demographics questions, and questions concerning patient understanding and anxiety surrounding the procedure. The purpose of the post-op survey will be to assess how well the video set expectations of the procedure and recovery process and will repeat questions asked pre-operatively. Survey responses will be analyzed to determine if there are beneficial trends and improvement in patient understanding and anxiety due to adjunct video usage. Primary Objective: The primary aim of the study is to determine if our animated video affects understanding and anxiety survey scores in patients undergoing DIEP breast reconstruction.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Scheduled for DIEP-flap breast reconstruction at Barnes Jewish Hospital.
- Speak English.
- Are 18 years old or older.
Who can't join
- Do not speak English, because the consent form, surveys, and video are only in English.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Scheduled to have DIEP-flap breast reconstruction at Barnes Jewish Hospital * Speak English * ≥ 18 years of age Exclusion Criteria: * Non-English speaking are excluded as the consent, questionnaires, and video are only available in English.
Study sites (1)
MO
- Washington University School of Medicine · St Louis, MO 63110Justin M Sacks, M.D., MBA, FACS · Study contact · 314-362-7388 · jmsacks@wustl.eduJustin M Sacks, M.D., MBA, FACS · Principal investigatorMore trials in St Louis