The Effect of Structured Education on Sexual Function and Sexual Quality of Life
NCT ID: NCT05808959
Last Updated: 2024-04-30
Study Results
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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COMPLETED
NA
34 participants
INTERVENTIONAL
2023-04-27
2024-04-05
Brief Summary
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Detailed Description
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Method This single-center, randomized controlled trial Participants and Sample The population of the study will be female patients who underwent TKA in the clinic where the study will be conducted. G\*Power (version 3.1.9.4) analysis was performed to determine sample size. it was planned to include 34 patients in total, 17 patients in each group.
Education Group; Their spouses will also participate in the structured sexual health education to be given to the women included in the training group and they will give their consent. Within the scope of the training, the definition of total hip replacement, the importance of sexual health, the definition of sexual intimacy, the ways of sexual intimacy, the general precautions that the patient should pay attention to in sexual life after TKA, the positions that should not be used during sexual intercourse in the early and late postoperative period, in the early postoperative period and In the late period, positions that can be used during sexual intercourse will be trained. It is thought that the training will take approximately 45-60 minutes in total.
Control Group; The participants in the control group will be given routine care of the clinic. Data Collection The data of the patient will be collected by the researchers face-to-face and through telephone interviews, using the Patient Sociodemographic and Medical Data Form, Female Sexual Function Questionnaire Index, Sexual Life Quality Scale-Female (CYQQ-F), Visual Analogue Scale (VAS).
Evaluation of Research Data SPSS 22.0 (IBM Corp., Armonk, NY) package program will be used in the evaluation of the data obtained from the research. Descriptive statistics will be presented as numbers, percentages, mean±standard deviation (SD), and median (min-max) values. Fisher's Exact Test or Pearson chi-square test will be used in the analysis of relationships between categorical variables. In the normality test, Shapiro Wilks test will be used when the number of samples in the group is less than 50, and Kolmogorov-Smirnov test will be used when it is large. In the analysis of the changes in the scores over time, the Kruskal Wallis test will be used if the measurements do not comply with the normal distribution, and the ANOVA test will be used if the measurements comply with the normal distribution. In the analysis of the difference between the scores of the two groups, the Mann-Whitney U test will be used if it does not fit the normal distribution, and the Student's t test will be used if it does. The reliability coefficient of the scales used in the study will be determined by calculating the Cronbach alpha coefficient. P values less than 0.05 will be considered statistically significant.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Education group
Structured training on sexual health will be given to patients in this group. After the discharge training given at the clinic in the postoperative period, the participants will be given structured training on sexual health. It is anticipated that the training will take approximately 30 minutes. Immediately after the training, feedback will be received from the patient through a question-answer activity, and areas that are not understood will be repeated. It is thought that the training will take approximately 45-60 minutes in total.
Education group
After the discharge training given at the clinic in the postoperative period, the participants will be given structured training on sexual health.
Control group
The clinic's routine discharge training will be applied to the participants in the control group.
No interventions assigned to this group
Interventions
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Education group
After the discharge training given at the clinic in the postoperative period, the participants will be given structured training on sexual health.
Eligibility Criteria
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Inclusion Criteria
* have no barriers to communicating,
* able to understand and speak Turkish,
* sexually active before and after TKA,
* with her husband,
* patients without sexual dysfunction will be included.
Exclusion Criteria
* having cancer,
* developing surgical site infection after TKA,
* do not complete the study,
* developing any complications during the working process,
* patients who lost their lives during the study will be excluded.
18 Years
65 Years
FEMALE
No
Sponsors
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Ankara University
OTHER
Responsible Party
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Hatice ÖNER CENGİZ
Assist. Prof.
Principal Investigators
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Hatice ÖNER CENGİZ
Role: STUDY_DIRECTOR
Ankara University
Locations
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Hatice ÖNER CENGİZ
Altındağ, Ankara, Turkey (Türkiye)
Countries
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Other Identifiers
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HONERCENGIZ
Identifier Type: -
Identifier Source: org_study_id
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