Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04780633
Other study ID # Approval No: 2017-3/20
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 15, 2017
Est. completion date October 15, 2017

Study information

Verified date February 2021
Source Ataturk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study was conducted to investigate the effect of a training program based on the PRECEDE-PROCEED Model on improving genital hygiene behaviors.It was carried out using experimental research design with pre-test and post-test, randomized and a control group. The study was conducted at Erzurum Saltuklu Family Health Center between June 2017 and January 2018. Of the women with genital infections, 120 women were included in the study, of which 60 were in the experimental group and 60 were in the control group. The data were collected by "Personal Information Form," "Genital Hygiene Knowledge, Attitude and Beliefs, Questionnaire" and "Genital Hygiene Behavior Inventory". In study, genital hygiene training intervention prepared according to the Precede-Proceed model was applied to the women in the experimental group. The women in the experimental group were measured at three different times: pre-test before training, post-test through training completition, and follow-up test after 4 weeks. The women in the control group did not receive any training intervention, the pre-test at the first encounter in the family health center and the post-test 5 weeks later.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date October 15, 2017
Est. primary completion date September 30, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria: - Between the ages of 18-49, - married, - At least primary school graduate, - No mental and communication problems, - No chronic disease, - Non-pregnant. Exclusion Criteria: - Women who have entered menopause, - Women who had received any training on genital hygiene before

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Precede-Proceed based Training Program on Genital Hygiene Behaviors
A Training Program for Genital Hygiene Behaviors prepared in line with the Precede-Proceed model was presented to the women in the experimental group. The trainings started one week after the pre-test data were collected and were conducted in a total of 5 sessions, each lasting an average of 40 minutes, once a week. At the end of the five-week training, a post-test was applied. In order to determine the behavior changes of the women in the experimental group, a follow-up test was applied 4 weeks after the training ended. At the end of the training, women were given a training booklet prepared by the researcher.

Locations

Country Name City State
Turkey Manolya Parlas Izmir None Selected

Sponsors (1)

Lead Sponsor Collaborator
Ataturk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary H1 hypothesis: PRECEDE-PROCEED training-based program affects on improving genital hygiene behavior. Linear regression analysis was performed to determine the factors that are independently effective in determining the Genital Hygiene Behavior Inventory (GHBI) score differences between the pre-test and post-test measurements of the women in the experimental group. 5 weeks