The Effect of Digital Technology-Supported Education on Patients Undergoing Breast Reconstruction After Mastectomy: A Randomized Controlled Study
Recruiting · NCT06166953 · Interventional (participants receive a specific treatment) · Lead sponsor: Baskent University
View the official record on ClinicalTrials.gov →Interventions studied
digital technology-supported education
What this trial is about
The goal of this randomized, controlled study is to test the effectiveness of digital technology-supported education on patients undergoing breast reconstruction after mastectomy.
Who can take part
Age range
18 Years to 75 Years
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
- Being diagnosed with stage 1, 2, or 3 breast cancer
- Planned to undergo immediate breast reconstruction after mastectomy for the first time
- Being between 18 to 75 years old
- Able to use smart phone
- Having smart phone with Android v5.0 or iOS v9.0 and above software, Bluetooth and internet connection
- Having no hearing or visual impairment
- Having no physical limitation
- Turkish speaking volunteers
Exclusion criteria
- Patients planned to undergo total abdominal hysterectomy and bilateral salpingo oophorectomy with immediate reconstruction after mastectomy
Where it is running
1 location listed.
- Başkent University Hospital - Ankara, Çankaya, Turkey (Türkiye)