Psychological Effect of Expectations and Body Image on Outcomes of Breast Reconstruction

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

A breast reconstruction after mastectomy, either due to breast cancer or a high lifetime risk for cancer, is performed to increase the patient's quality of life. However, there are studies that show that some women regret their decision to have breast reconstruction. There are also studies demonstrating similarities in the general patterns of psychosocial adjustment and quality of life among women with breast cancer who have undergone breast-conserving surgery, mastectomy alone, and mastectomy combined with breast reconstruction. Hence, it is unclear which women actually benefit from a breast reconstruction. The concept of quality of life is connected to patient satisfaction and body image/investment. Therefore, the aim of this project is to examine the effects of patient expectations and body image on the patient reported outcomes of breast reconstruction, to improve preoperative information and postoperative care for women considering a breast reconstruction.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Biological women with breast cancer or high risk for breast cancer who want post-mastectomy breast reconstruction

• Age \> 18 years

Locations
Other Locations
Sweden
Sahlgrenska university hospital
RECRUITING
Gothenburg
Contact Information
Primary
Emma Hansson, PhD
emma.em.hansson@vgregion.se
+46313421000
Time Frame
Start Date: 2021-02-01
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 500
Treatments
Immediate breast reconstruction
Women undergoing immediate breast reconstruction due to breast cancer or a high risk for breast cancer
Delayed breast reconstruction
Women undergoing delayed breast reconstruction due to breast cancer or a high risk for breast cancer
Related Therapeutic Areas
Sponsors
Leads: Vastra Gotaland Region

This content was sourced from clinicaltrials.gov