ClinicalTrials.Veeva

Menu

Post-Hysterectomy Nursing Support Program

S

Suleyman Demirel University

Status

Completed

Conditions

Hysterectomy

Treatments

Other: Nursing Support Program

Study type

Interventional

Funder types

Other

Identifiers

NCT05063864
KYilmaz

Details and patient eligibility

About

Objective: This study was conducted to evaluate the effectiveness of the nursing support program developed for women undergoing hysterectomy.

Background: Hysterectomy is an important surgical intervention that affects women physically, sexually and psychosocially.

Method: The study is a single blind, randomized controlled study conducted at the Department of Obstetrics and Gynecology in a university hospital between November 2017 and November 2018. 60 women who had hysterectomy were divided into experimental and control groups and It was evaluated on the 1-2 day, 6-7 day and 2nd month. In the study, the nursing support program was applied only to women in the experimental group.

Full description

Aim: This study was conducted to evaluate the effectiveness of the nursing support program developed for women who had hysterectomy.

Methods: A prospective, randomised controlled study was conducted in the gynaecology clinic of a university hospital between November 2017 and November 2018. It was conducted in a single-blind, randomised controlled trial with a total of 60 women in the experimental and control groups. A nursing support program had been developed for women who have had a hysterectomy. The program developed for the experimental group and the routine program for routine maintenance and control group were applied. The initial evaluation was carried out postoperative on the 1st-2nd day, the second assessment was carried out on the 6th-7th day and the third evaluation was carried out at 2 months. The first interview was carried out in the hospital, and the second and third interviews were carried out with home visits. The sociodemographic data form, postoperative evaluation form, Female Sexual Function Index (FSFI), Epidemiological Studies and Central Depression Scale (EAMDS), Menopausal Symptoms Evaluation Scale (MSDS) and SF-12 quality of life scale were used to collect data.

Enrollment

60 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis benign hysterectomy and bilateral oophorectomy
  • Having no communication problems.

Exclusion criteria

  • Clinical diagnosis vaginal hysterectomy
  • Clinical diagnosis psychiatric disorders and therefore used drugs

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Nursing Support Program
Experimental group
Description:
the group that applied the nursing support program
Treatment:
Other: Nursing Support Program
No Nursing Support Program
No Intervention group
Description:
the group that did not receive a nursing support program

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems