Sexual Functıon in Young Women After Breast Cancer Surgery

NCT ID: NCT06966791

Last Updated: 2025-05-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

52 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-30

Study Completion Date

2026-06-30

Brief Summary

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The aim of this observational study was to analyse sexual function in young women after breast cancer surgery. The main question it aims to answer is Sexual function in young women after breast cancer surgery changes during the one-year follow-up period. Participants will answer demographic information, Female Sexual Function Scale, Breast-Q and Body Perception Scale about their sexual function, quality of life and body perception. These will be recorded before surgery and repeated 6 weeks, 6 months and 1 year after surgery.

Detailed Description

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As a result of the power analysis of the preliminary study conducted with the participation of 9 cases; it was calculated that 80% power could be obtained at 95% confidence level when at least 47 people were included in the study. However, considering that the results of the preliminary study will not be conclusive, it is planned to complete the study with at least 52 people by taking 10% more participants. The data will be analysed with SPSS 25.0 package programme. Continuous variables will be given as mean ± standard deviation and categorical variables as number and percentage. Repeated measures ANOVA test, Kruskal-Wallis test or Friedman test will be used according to the parametric test assumptions.

Conditions

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Breast Cancer Surgery Young Adult Females

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Young women with breast cancer

Sexually active young women scheduled for breast cancer surgery

No intervention will be performed as part of this study. However, regardless of the study, all participants will have breast cancer surgery

Intervention Type OTHER

No intervention will be performed as part of this study. However, regardless of the study, all participants will have breast cancer surgery and other breast cancer treatments.

Interventions

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No intervention will be performed as part of this study. However, regardless of the study, all participants will have breast cancer surgery

No intervention will be performed as part of this study. However, regardless of the study, all participants will have breast cancer surgery and other breast cancer treatments.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals scheduled for surgery for breast cancer
* Accepting to participate in the study
* Being sexually active in the last 1 year
* Continuation of menstruation

Exclusion Criteria

* Previous breast cancer surgery
* Previous history of breast cancer
* History of any other cancer
* Refusal to participate in the study
* Refusal to continue working
* Problems in her relationship with her partner
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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ATİYE KAŞ ÖZDEMİR

OTHER

Sponsor Role lead

Responsible Party

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ATİYE KAŞ ÖZDEMİR

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Pamukkale University

Denizli, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Atiye KAŞ ÖZDEMİR, Lecturer PhD

Role: CONTACT

+902584151515

Facility Contacts

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Atiye KAŞ ÖZDEMİR, Lecturer, PhD

Role: primary

+902584151515

Other Identifiers

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E-60116787-020-631173

Identifier Type: -

Identifier Source: org_study_id

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