Sexual Functıon in Young Women After Breast Cancer Surgery
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: No intervention will be performed as part of this study. However, regardless of the study, all participants will have breast cancer surgery.
- Кому может быть актуально
- Состояния в реестре: Breast Cancer Surgery, Young Adult Females. Базовые параметры: 18 лет — 50 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Turkey (Türkiye)
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Examınatıon of Sexual Functıon in Young Women After Breast Cancer Surgery
Обзор
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.
Подробное описание
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.
Вмешательства
- Другое 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.
Первичные конечные точки
- Sexual function [Срок оценки: It is planned to repeat the measurements 4 times: before, 6 weeks, 6 months and 12 months after breast cancer surgery.]
Вторичные конечные точки (2)
- Quality of life of participants [Срок оценки: It is planned to repeat the measurements 4 times: before, 6 weeks, 6 months and 12 months after breast cancer surgery.]
- Participants' body perception [Срок оценки: It is planned to repeat the measurements 4 times: before, 6 weeks, 6 months and 12 months after breast cancer surgery.]
Критерии участия
Критерии включения
- Individuals scheduled for surgery for breast cancer
- Accepting to participate in the study
- Being sexually active in the last 1 year
- Continuation of menstruation
Критерии исключения
- 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
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Turkey (Türkiye) · 1 центр
- Pamukkale University — Denizli
Идентификаторы
NCT: NCT06966791 · E-60116787-020-631173