- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07341035
Genital Hygiene Education on Women's Self-Care Agency and Genital Hygiene Behaviors
The Effect of Video-Assisted Genital Hygiene Education on Women's Self-Care Agency and Genital Hygiene Behaviors
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Çankırı, Turkey (Türkiye)
- Çankırı Karatekin University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
- Inclusion Criteria: Patients who were diagnosed with urinary tract infection by a physician, who had no hearing difficulties and visual loss, and who could communicate were included in the study.
- Exclusion Criteria: Patients who were not diagnosed with urinary tract infection, who were hard of hearing, visually impaired, unable to communicate, unable to maintain genital hygiene and who refused to participate in the study were excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Groups
Experimental Group; the women in the experimental group were provided with the relevant forms and asked to complete the Data Collection Form for Women, Self-Care Agency Scale, and Genital Hygiene Behaviors Scale for the pretest. Afterward, they received information about the importance of genital hygiene, key points to consider during genital hygiene, and watched a training video developed by the researchers. This video demonstrated genital hygiene practices on a human model, with the researcher explaining and demonstrating the steps in a practical manner. Following the video training, participants completed the same forms again (Data Collection Form for Women, Self-Care Agency Scale, and Genital Hygiene Behaviors Scale) for the midterm test. To assess the long-term effects of the training, the participants were asked to complete the same forms 8 weeks after the training. |
The women in the experimental group were provided with the relevant forms and asked to complete the Data Collection Form for Women, Self-Care Agency Scale, and Genital Hygiene Behaviors Scale for the pretest. Afterward, they received information about the importance of genital hygiene, key points to consider during genital hygiene, and watched a training video developed by the researchers. This video demonstrated genital hygiene practices on a human model, with the researcher explaining and demonstrating the steps in a practical manner. Following the video training, participants completed the same forms again (Data Collection Form for Women, Self-Care Agency Scale, and Genital Hygiene Behaviors Scale) for the midterm test. To assess the long-term effects of the training, the participants were asked to complete the same forms 8 weeks after the training. |
|
No Intervention: Control Groups
Control Group; the women in the control group were informed about the forms and asked to complete the Data Collection Form for Women, Self-Care Agency Scale, and Genital Hygiene Behaviors Scale for the pretest.
They were also informed about the importance of genital hygiene and key points to consider, but no video-assisted training was provided.
The control group filled out the same forms for the midterm and posttest assessments, at the same times as the experimental group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-Care Agency Level
Time Frame: Baseline (Pretest, Week 1), immediately after the intervention (Posttest, Week 2), and 3-month follow-up
|
Self-care agency will be assessed using the Self-Care Agency Scale, developed by Kearney and Fleischer (1979) and validated in Turkish by Nahcivan (2004). The scale consists of 35 items rated on a 5-point Likert scale (0-4), with a total score range of 0 to 140. Higher scores indicate higher levels of self-care agency. |
Baseline (Pretest, Week 1), immediately after the intervention (Posttest, Week 2), and 3-month follow-up
|
|
Genital Hygiene Behaviors
Time Frame: Baseline (Pretest, Week 1), immediately after the intervention (Posttest, Week 2), and 3-month follow-up
|
Genital hygiene behaviors will be measured using the Genital Hygiene Behaviors Scale, validated by Karahan (2017). The scale includes 23 items rated on a 5-point Likert scale (1-5), with total scores ranging from 23 to 115. Higher scores indicate more positive genital hygiene behaviors. |
Baseline (Pretest, Week 1), immediately after the intervention (Posttest, Week 2), and 3-month follow-up
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Dahodwala M, Geransar R, Babion J, de Grood J, Sargious P. The impact of the use of video-based educational interventions on patient outcomes in hospital settings: A scoping review. Patient Educ Couns. 2018 Dec;101(12):2116-2124. doi: 10.1016/j.pec.2018.06.018. Epub 2018 Jun 30.
- Massimi A, De Vito C, Brufola I, Corsaro A, Marzuillo C, Migliara G, Rega ML, Ricciardi W, Villari P, Damiani G. Are community-based nurse-led self-management support interventions effective in chronic patients? Results of a systematic review and meta-analysis. PLoS One. 2017 Mar 10;12(3):e0173617. doi: 10.1371/journal.pone.0173617. eCollection 2017.
- Mancuso G, Midiri A, Gerace E, Marra M, Zummo S, Biondo C. Urinary Tract Infections: The Current Scenario and Future Prospects. Pathogens. 2023 Apr 20;12(4):623. doi: 10.3390/pathogens12040623.
- Cox S, Vleeming M, Giorgi W, Dinant GJ, Cals J, de Bont E. Patients' Experiences, Expectations, Motivations, and Perspectives around Urinary Tract Infection Care in General Practice: A Qualitative Interview Study. Antibiotics (Basel). 2023 Jan 24;12(2):241. doi: 10.3390/antibiotics12020241.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 06-07-2023/8
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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