The Effect of Hysterectomy Education and Counseling on Stress, Quality of Life, and Dyadic Adjustment
13 juni 2026 uppdaterad av: Merve Keser, Hasan Kalyoncu University
The Effect of Counseling and Education Given to Women Undergoing Hysterectomy on Dyadic Adjustment, Perceived Stress, and Quality of Life: A Randomized Controlled Trial
The aim of this study was to evaluate the effects of postoperative education and counseling provided to women undergoing hysterectomy on dyadic adjustment, perceived stress, and quality of life.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This randomized controlled trial was designed to evaluate the effects of postoperative education and counseling on perceived stress, quality of life, and dyadic adjustment among women undergoing hysterectomy.
The study was conducted in the gynecology ward of Çukurova University Balcalı Hospital between September 2024 and February 2025.
A total of 60 women were randomly assigned to either an intervention group (n=30) or a control group (n=30) using a simple randomization method.
Data were collected using the Sociodemographic Data Questionnaire, the Perceived Stress Scale (PSS), the SF-12 Quality of Life Scale (SF-12 QoL), and the Revised Dyadic Adjustment Scale (RDAS).
Women in the intervention group received structured hysterectomy education on the first postoperative day and weekly counseling sessions for four weeks after discharge.
Women in the control group received routine postoperative care.
Outcome assessments were performed at baseline and five weeks after enrollment.
Studietyp
Interventionell
Inskrivning (Faktisk)
60
Fas
- Inte tillämpbar
Kontakter och platser
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Studieorter
-
-
Şahinbey/gaziantep
-
Gaziantep, Şahinbey/gaziantep, Turkiet (Türkiye), 27410
- Hasan Kalyoncu University, Graduate Education Institute, Department of Nursing
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Ja
Beskrivning
Inclusion Criteria:
Women undergoing hysterectomy Aged 18 years and older Married and living with their spouse Able to communicate in Turkish
Exclusion Criteria:
Women with diagnosed psychiatric disorders Women with severe postoperative complications requiring intensive care
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Hysterectomy Education and Counseling
Women in this group received structured hysterectomy education on the first postoperative day and weekly counseling sessions for four weeks following discharge, in addition to routine postoperative care.
|
Participants received structured hysterectomy education on the first postoperative day and weekly counseling sessions for four weeks after discharge.
Education and counseling focused on postoperative recovery, complication prevention, physical activity, sexual health, emotional support, healthy lifestyle behaviors, and adaptation following hysterectomy.
|
|
Experimentell: control group
Women in this group received routine postoperative care.
No structured education or counseling was provided during the study period.
Follow-up assessments were conducted five weeks after the pre-test, and an educational booklet was provided after completion of the post-test.
|
Participants received structured hysterectomy education on the first postoperative day and weekly counseling sessions for four weeks after discharge.
Education and counseling focused on postoperative recovery, complication prevention, physical activity, sexual health, emotional support, healthy lifestyle behaviors, and adaptation following hysterectomy.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Perceived Stress Scale (PSS)
Tidsram: Baseline and 5 weeks after intervention
|
Change in perceived stress levels measured using the Perceived Stress Scale.
|
Baseline and 5 weeks after intervention
|
|
SF-12 Quality of Life Scale
Tidsram: Baseline and 5 weeks after intervention
|
Change in physical and mental quality of life measured using the SF-12 Quality of Life Scale.
|
Baseline and 5 weeks after intervention
|
|
Revised Dyadic Adjustment Scale (RDAS)
Tidsram: Baseline and 5 weeks after intervention
|
Change in dyadic adjustment measured using the Revised Dyadic Adjustment Scale.
|
Baseline and 5 weeks after intervention
|
Samarbetspartners och utredare
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Sponsor
Utredare
- Huvudutredare: merve keser, Hasan Kalyoncu University, Graduate Education Institute, Department of Nursing
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
1 september 2024
Primärt slutförande (Faktisk)
1 februari 2025
Avslutad studie (Faktisk)
1 mars 2026
Studieregistreringsdatum
Först inskickad
10 juni 2026
Först inskickad som uppfyllde QC-kriterierna
13 juni 2026
Första postat (Faktisk)
16 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
16 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
13 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- 2024/98
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