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The Effect of Sexual Counselling Based on PLISSIT and BETTER Model After Hysterectomy

NCT06609096 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2025-09-03

No results posted yet for this study

Summary

Sexuality is affected by several physiological, cultural, social, and psychological factors. Hysterectomy is one of the factors that affects sexuality. Evidence suggests that hysterectomy, affects the sexual function of women. Therefore, this study aimed to evaluate the effect of sexual counseling based on the PLISSIT and BETTER models on sexual function and quality of sexual life of women after hysterectomy. This study is a randomized controlled trial with a three-arm parallel design. One of the experimental groups will receive sexual counseling based on the PLISSIT model and the other will receive sexual counseling based on the BETTER model. The control group will not receive any intervention. The difference between the intervention groups and the control group will be evaluated.

Conditions

  • Hysterectomy
  • PLISSIT Model
  • Sexual Health Quality of Life
  • Sexual Function
  • Sexual Health

Interventions

BEHAVIORAL

Sexual counseling based on the PLISSIT model

Four sessions of sexual counseling based on the PLISSIT model will be provided. The intervention consisted of four consecutive sessions, with one session per week. Each session is 30 minutes on average.

BEHAVIORAL

Sexual counseling based on the BETTER model

A total of four sessions of sexual counseling based on the BETTER model will be provided. The intervention consists of four consecutive sessions, one session per week. Each session is 30 minutes on average.

Sponsors & Collaborators

  • Gazi University

    collaborator OTHER

  • Kutahya Health Sciences University

    lead OTHER

Principal Investigators

  • Sevil Çiçek Özdemir, Asst. Prof. · Kütahya Health Sciences University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-23
Primary Completion
2025-01-01
Completion
2025-03-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06609096 on ClinicalTrials.gov