Cancer
Conditions
Keywords
breast cancer
Brief summary
The use of luteinizing hormone-releasing hormone agonists(LHRHa) to suppress ovarian function is a common strategy for treating premenopausal, hormone receptor-positive breast cancer. However, this approach can lead to more severe and prolonged menopausal symptoms, which can further impact intimate relationships and sexual function. Sexual coercion, encompassing both overt and subtle forms of pressure, is a significant global public health concern that threatens individual well-being.
Detailed description
Objective: The use of luteinizing hormone-releasing hormone agonists(LHRHa) to suppress ovarian function is a common strategy for treating premenopausal, hormone receptor-positive breast cancer. However, this approach can lead to more severe and prolonged menopausal symptoms, which can further impact intimate relationships and sexual function. Sexual coercion, encompassing both overt and subtle forms of pressure, is a significant global public health concern that threatens individual well-being. Methods: This study is a randomized controlled study. In this study, the validated Turkish version of the Sexual Coercion in Intimate Relationship Scale was utilized to investigate whether patients receiving LHRHa therapy experienced higher rates of sexual sexual coercion compared to those taking tamoxifen. The study included 40 patients using LHRHa and 39 patients using tamoxifen. The instrument assessed partner sexual coercion across three subdomains: resource manipulation/sexual coercion, commitment manipulation, and defection threat.
Interventions
BEHAVIORALSexual Coercion
This study aimed to investigate whether patients receiving LHRHa treatment experienced sexual coercion at a higher rate than those using tamoxifen. 40 patients using LHRHa and 39 patients using tamoxifen were included in the study.
Sponsors
Canan Kas
Study design
Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
* being over 18 years of age * willingness to participate in this study * having received treatment for breast cancer * having a history of breast cancer surgery * having an active relationship with a spouse or partner.
Exclusion criteria
* having any neuropsychiatric disorder * having any mental illness * having a history of gynecological surgery * currently receiving active chemotherapy or less than 3 months since completing chemotherapy * receiving treatment for metastatic disease * The use of selective serotonin reuptake inhibitors
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| LHRHa | for 10 months | It was examined whether patients receiving LHRHa treatment were exposed to sexual pressure. |
| Tamoxifen | for 10 months | It was examined whether patients receiving tamoxifen treatment were exposed to sexual pressure. |
Countries
Turkey (Türkiye)
Outcome results
None listed