Digital education for patients having breast reconstruction after mastectomy
The Effect of Digital Technology-Supported Education and Monitoring on Anxiety, Pain, Sleep and Quality of Life in Patients Undergoing Immediate Breast Reconstruction After Mastectomy: A Randomized Controlled Study
This study tests whether using digital education tools can help women feel less anxious and better understand their options after having breast reconstruction surgery following a mastectomy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 38 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Baskent University Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Ankara, Çankaya) |
| Trial ID | NCT06166953 on ClinicalTrials.gov |
What this trial studies
This randomized controlled study aims to evaluate the effectiveness of digital technology-supported education for patients undergoing breast reconstruction following mastectomy due to breast cancer. The study focuses on providing comprehensive educational resources through mobile applications to help patients manage preoperative anxiety and postoperative complications. By utilizing various digital tools, the study seeks to enhance patients' understanding of their treatment options and improve their overall quality of life. Participants will be monitored for psychological and physical outcomes related to their surgery.
Who should consider this trial
Good fit: Ideal candidates are Turkish-speaking individuals aged 18 to 75 diagnosed with stage 1, 2, or 3 breast cancer who are planning to undergo immediate breast reconstruction after mastectomy.
Not a fit: Patients who are undergoing total abdominal hysterectomy and bilateral salpingo oophorectomy with immediate reconstruction after mastectomy may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the psychological well-being and recovery outcomes for patients undergoing breast reconstruction.
How similar studies have performed: Other studies have shown promising results with digital education approaches in various medical fields, indicating potential success for this novel application in breast cancer care.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Ankara, Çankaya
- Başkent University Hospital — Ankara, Çankaya, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Aylin Günay, MSc,RN
- Email: aylingunay@baskent.edu.tr
- Phone: +905330888921
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.