Ignite Creation Date:
2024-05-06 @ 7:05 PM
Last Modification Date:
2024-10-26 @ 3:00 PM
Study NCT ID:
NCT05898386
Status:
COMPLETED
Last Update Posted:
2023-06-26
First Post:
2023-03-21
Brief Title:
Education and Counseling Program Based on the Health Promotion Model
Sponsor:
Ankara Yildirim Beyazıt University
Organization:
Ankara Yildirim Beyazıt University
Study Overview
Official Title:
The Effect of Education and Counseling Program Based on the Health Promotion Model on Self-Esteem Sexual Satisfaction and Quality of Life in Women With Urinary Incontinence
Status:
COMPLETED
Status Verified Date:
2023-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The first phase of the study was carried out to determine the prevalence and risk factors of urinary incontinence in non-menopausal women over 18 years of age registered in a Family Health Center
The second phase of the study was carried out to examine the effects of the education and counseling program based on the Penders Health Promotion Model on womens self-esteem sexual satisfaction and quality of life in women with urinary incontinence
Research Questions
What is the prevalence of UI in non-menopausal women over the age of 18 who are registered with the Family Health Center What are the risk factors for urinary incontinence
Research Hypotheses
H1 There is a difference between the urinary incontinence severity levels of women who received and did not receive education and counseling program based on Penders health promotion model
H2 There is a difference between the self-esteem levels of women who received and did not receive a training and counseling program based on Penders health promotion model
H3 There is a difference between the sexual satisfaction levels of women who received and did not receive the training and counseling program based on Penders health promotion model
H4 There is a difference between the quality of life levels of women who received training and counseling programs based on Penders health promotion model and those who did not
In the second stage of the study the Training and Counseling Program Based on Penders Health Promotion Model and Home Monitoring and Counseling Program were applied to the intervention group which was prepared according to Penders Health Promotion Model
During the three-month period the intervention group received 3 home visits one two and three months after the training program and 3 phone calls 15 days after the training program and each home visit
No intervention was made in the control group Data collection forms were applied simultaneously with the intervention group and they were reminded that they were in the research by making a phone call
The second phase of the study was carried out to examine the effects of the education and counseling program based on the Penders Health Promotion Model on womens self-esteem sexual satisfaction and quality of life in women with urinary incontinence
Research Questions
What is the prevalence of UI in non-menopausal women over the age of 18 who are registered with the Family Health Center What are the risk factors for urinary incontinence
Research Hypotheses
H1 There is a difference between the urinary incontinence severity levels of women who received and did not receive education and counseling program based on Penders health promotion model
H2 There is a difference between the self-esteem levels of women who received and did not receive a training and counseling program based on Penders health promotion model
H3 There is a difference between the sexual satisfaction levels of women who received and did not receive the training and counseling program based on Penders health promotion model
H4 There is a difference between the quality of life levels of women who received training and counseling programs based on Penders health promotion model and those who did not
In the second stage of the study the Training and Counseling Program Based on Penders Health Promotion Model and Home Monitoring and Counseling Program were applied to the intervention group which was prepared according to Penders Health Promotion Model
During the three-month period the intervention group received 3 home visits one two and three months after the training program and 3 phone calls 15 days after the training program and each home visit
No intervention was made in the control group Data collection forms were applied simultaneously with the intervention group and they were reminded that they were in the research by making a phone call
Detailed Description:
The research was carried out in two stages
In the first phase of the study in a cross-sectional research design in order to determine the prevalence and risk factors of urinary incontinence in women who are over 18 years old and who are not menopausal registered in a Family Health Center In this study a pretest-posttest randomized controlled experimental research design was conducted to evaluate the effect of education and counseling program based on Penders Health Promotion Model on self-esteem sexual satisfaction and quality of life in women with second-stage urinary incontinence
In the first phase of the study 1042 women over the age of 18 who were registered at the Family Health Center and who did not go through menopause were included
In the first stage the data It was collected between 18 January 2021 and 31 May 2021 using the Questionnaire on Descriptive Characteristics International Incontinence Inquiry Form and Incontinence Severity Index
The second stage of the study continued with 46 women who met the sample selection criteria for the second stage
After the pre-test was completed 46 women were assigned to the intervention and control groups M23 F23 by stratified block randomization and stratified according to urinary incontinence severity mild moderate
In the second stage of the research the data Between September 24 2021 and January 13 2022 International Incontinence Inquiry Form Incontinence Severity Index Information Form Based on Penders Health Promotion Model Self-Esteem Sub-Scale Golombok-Rust Sexual Satisfaction Scale- It was collected using the Female Form Incontinence Quality of Life Scale Self-EfficacyEfficacy Scale
In the second stage of the study the Training and Counseling Program Based on Penders Health Promotion Model and Home Monitoring and Counseling Program were applied to the intervention group which was prepared according to Penders Health Promotion Model
During the three-month period the intervention group received 3 home visits one two and three months after the training program and 3 phone calls 15 days after the training program and each home visit
No intervention was made in the control group Data collection forms were applied simultaneously with the intervention group and they were reminded that they were in the research by making a phone call
In both stages of the study the forms and scales were filled by the women themselves and the women were guided during this period
Frequency percentage and descriptive statistics for data evaluation Shapiro-Wilk Test Independent Samples T-Test Repeated Measurements Anova Test Chi-square Test of Independence Fisher Test Cochran-Q Test Mann-Whitney U Test McNemar Test Friedman Test and Marginal Homogeneity Test were used
In the first phase of the study in a cross-sectional research design in order to determine the prevalence and risk factors of urinary incontinence in women who are over 18 years old and who are not menopausal registered in a Family Health Center In this study a pretest-posttest randomized controlled experimental research design was conducted to evaluate the effect of education and counseling program based on Penders Health Promotion Model on self-esteem sexual satisfaction and quality of life in women with second-stage urinary incontinence
In the first phase of the study 1042 women over the age of 18 who were registered at the Family Health Center and who did not go through menopause were included
In the first stage the data It was collected between 18 January 2021 and 31 May 2021 using the Questionnaire on Descriptive Characteristics International Incontinence Inquiry Form and Incontinence Severity Index
The second stage of the study continued with 46 women who met the sample selection criteria for the second stage
After the pre-test was completed 46 women were assigned to the intervention and control groups M23 F23 by stratified block randomization and stratified according to urinary incontinence severity mild moderate
In the second stage of the research the data Between September 24 2021 and January 13 2022 International Incontinence Inquiry Form Incontinence Severity Index Information Form Based on Penders Health Promotion Model Self-Esteem Sub-Scale Golombok-Rust Sexual Satisfaction Scale- It was collected using the Female Form Incontinence Quality of Life Scale Self-EfficacyEfficacy Scale
In the second stage of the study the Training and Counseling Program Based on Penders Health Promotion Model and Home Monitoring and Counseling Program were applied to the intervention group which was prepared according to Penders Health Promotion Model
During the three-month period the intervention group received 3 home visits one two and three months after the training program and 3 phone calls 15 days after the training program and each home visit
No intervention was made in the control group Data collection forms were applied simultaneously with the intervention group and they were reminded that they were in the research by making a phone call
In both stages of the study the forms and scales were filled by the women themselves and the women were guided during this period
Frequency percentage and descriptive statistics for data evaluation Shapiro-Wilk Test Independent Samples T-Test Repeated Measurements Anova Test Chi-square Test of Independence Fisher Test Cochran-Q Test Mann-Whitney U Test McNemar Test Friedman Test and Marginal Homogeneity Test were used
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None