PRECEDE-PROCEED Model-based Program on Genital Hygiene Behaviors

Sponsor
Ataturk University (Other)
Overall Status
Completed
CT.gov ID
NCT04780633
Collaborator
(none)
120
1
2
4
29.9

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Precede-Proceed based Training Program on Genital Hygiene Behaviors
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effects of a PRECEDE-PROCEED Model-based Program on Genital Hygiene Behaviors: A Randomized Controlled Trial
Actual Study Start Date :
Jun 15, 2017
Actual Primary Completion Date :
Sep 30, 2017
Actual Study Completion Date :
Oct 15, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Precede-Proceed based Training Program

The experimental group is the group in which five training sessions interventions are applied.

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.

No Intervention: Control group

The control group is the group in which have no educational intervention.

Outcome Measures

Primary Outcome Measures

  1. H1 hypothesis: PRECEDE-PROCEED training-based program affects on improving genital hygiene behavior. [5 weeks]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 49 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Manolya Parlas Izmir None Selected Turkey 35210

Sponsors and Collaborators

  • Ataturk University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Manolya Parlas, Principal Investigator, Ataturk University
ClinicalTrials.gov Identifier:
NCT04780633
Other Study ID Numbers:
  • Approval No: 2017-3/20
First Posted:
Mar 3, 2021
Last Update Posted:
Mar 3, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Manolya Parlas, Principal Investigator, Ataturk University

Study Results

No Results Posted as of Mar 3, 2021