Hybrıd Educatıon Based on Psychodynamıc Nursıng Theory of Women Undergoıng Mastectomy (Mastectomy)
The Effect of Hybrıd Educatıon Based on Psychodynamıc Nursıng Theory on Body Value, Socıal Appearance Anxıety and Sexual Qualıty of Lıfe of Women Undergoıng Mastectomy
Our study aims to investigate the effects of planned hybrid (web-based and face-to-face) group training to be given to women with mastectomies based on Psychodynamic nursing theory, on women's body value, social appearance anxiety and sexual life quality.
Power analysis was performed for the study group of the study and intervention and control groups were created by randomization method (intervention group n = 30, control group n = 30). The study will be applied as a pretest-posttest experimental intervention method. In order to make an evaluation before and after the planned hybrid training, the situations that are most affected by women after mastectomy were analyzed in line with the literature and the data were collected from the Sociodemographic Characteristics Form, Body Value Scale-2, Social Appearance Anxiety Scale (SAAS), Sexual Quality of Life Scale-Female (SQOL-W). will be collected using. A standard information brochure containing information about mastectomy will be given to the intervention and control groups after the pre-test. Then, hybrid group training based on Psychodynamic Nursing Theory will be given to the intervention group by the researcher. A Whatsapp group will also be established to enable patients to communicate and ask questions. During the process, 9 web-based and 3 face-to-face group trainings will be held. A posttest will be administered to both groups at the end of the last group training, and a permanence test will be administered 1 month later via Google surveys on the Whatsapp group. SPPS program and Pearson Chi-square test, Independent Samples Test, McNemar, Pearson Chi-square test, ANOVA (Repeated Measures ANOVA) will be used to analyze the data. As a result of the study, in line with the research findings, the effect of hybrid group training based on Psychodynamic Nursing Theory on the body value, social appearance anxiety and sexual life quality of women who have undergone mastectomy will be evaluated.
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
Ortahisar
-
Trabzon, Ortahisar, Turkije (Türkiye), 61500
- Karadeniz Technıcal Unıversity
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Ages 18-55, no communication problems,
- Proficiency in Turkish,
- Internet access via mobile phone or computer,
- At least 6 months must have passed since mastectomy surgery (mourning period),
- Active sexual life,
- Agreement to participate in the study.
Exclusion Criteria:
- Having hearing, vision, or comprehension problems,
- Having undergone breast reconstruction,
- Receiving any psychiatric diagnosis during the research process,
- Participating in any training, research, or social activity group that may affect the outcome variables during the research process.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ondersteunende zorg
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: initiative
First, preliminary test data was collected.
The researcher provided hybrid group training based on Psychodynamic Nursing Theory to the intervention group.
Throughout the process, 9 web-based and 3 in-person group training sessions were conducted.
A post-test was administered after the last group training session, and a retention test was administered one month later.
|
The intervention group received hybrid group education sessions based on Psychodynamic Nursing Theory.
A total of 12 sessions were conducted, including 9 web-based sessions and 3 face-to-face group sessions.
|
|
Geen tussenkomst: control
First, preliminary test data was collected.
A standard information brochure was provided.
Simultaneously with the intervention group, a post-test and retention test were administered.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Body Value Scale Score
Tijdsspanne: 12 weeks
|
Body esteem was assessed using the Body Esteem Scale (BES).
Scores were compared between intervention and control groups.
|
12 weeks
|
|
Social Appearance Anxiety Scale Score
Tijdsspanne: 12 weeks
|
Social appearance anxiety was measured using the Social Appearance Anxiety Scale (SAAS).
Scores were compared between groups.
|
12 weeks
|
|
Sexual Quality of Life Scale Score
Tijdsspanne: 12 weeks
|
Sexual quality of life was assessed using the Sexual Quality of Life-Female (SQOL-F) Scale.
Scores were compared between groups
|
12 weeks
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- E-13562490-050.01.04-562578
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .