- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06439680
HASCV-R" Health Programme: a RCT
The Effect of " HASCV-R" Training Program on Women's Health Promotion and Protective Behaviors: A Randomized Controlled Experimental Study
The goal of this randomized controlled trial: is to determine the effect of " HASCV-R " health programme on the health promoting and protective behaviours of the women. The main question it aims to answer are:
• Does the HASCV-R program, positively affect the health promoting and protective behaviours of women? The health program was given to the women in the experimental group in five sessions of 40 minutes each for five weeks. The program was implemented to 45 women. After obtaining consent from women, Data were gathered with all participants at the available time and places.
The data were collected from the control and experimental groups at two different times, prior to the program was implemented and 3 months after the program was implemented.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Positive health behaviors aimed at improving health refer to individuals' conscious efforts to protect and improve their own health and the health of other individuals. Examples of positive health behaviors include eating adequate and balanced nutrition, paying attention to sleep patterns, doing physical activity, staying away from stress, having regular health checks, and communicating effectively and positively with people. In order for individuals to acquire positive health behaviors, they need to have an idea about all of these behaviors and turn the knowledge they have acquired into behavior. Health professionals undoubtedly have a large share in the formation of this health awareness, as well as in the treatment of diseases, as well as in protecting health and avoiding risky health behaviors.
It is seen that in developed societies, the planning, implementation and evaluation stages of health promotion programs in health services are carried out by professional nurses. The group that will ensure the development of health, informing and guiding healthy behaviors are nurses who provide professional care in health institutions. There are training programs to improve women's health in the literature, but there is no training program that is both health-promoting and health-protective. Considering the impact of nurses on health education and creating behavioral change, their knowledge on this subject and their ability to transfer this to public health is of great importance. In addition, considering that a healthy lifestyle has become so important today, the unique value of the study is that the training program to be developed includes behaviors that promote and protect women's health. This research was planned to evaluate the effect of the "HASCV-R" training program on women's health-promoting and protective behaviors.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Yozgat, Turkey
- Yozgat Bozok University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- volunteering to participate in the study,
- be between the ages of 18 and 49,
- being a women,
- no communication barriers (to communicate with any problem such as hearing problem, speech impediment),
- to be married
Exclusion Criteria:
being younger than 18 or over 49,
- be man,
- ınability to communicate with any problem such as hearing problem, speech impediment,
- living single,
- refusing to participate in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: control
|
HASCV-R program "Healthy nutrition, Active life, Ways to cope with Stress, Cancer and cancer screening, Vaccination - Reproductive health" Training programme
|
|
Experimental: experimental
Experimental: experimental This study was carried out with the women living in Tokat province.
Trainings and measurement tools in the HASCV-R programme was implemented in the Hanımeli culture and art centers.
|
HASCV-R program "Healthy nutrition, Active life, Ways to cope with Stress, Cancer and cancer screening, Vaccination - Reproductive health" Training programme
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Questionnaire form
Time Frame: prior to the program was implemented and 3 months after the program was implemented
|
This form, developed by the researchers based on the literature, includes the socio-demographic characteristics of the women such as age, education status, income status, etc.)
|
prior to the program was implemented and 3 months after the program was implemented
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health Promoting and Protective Behaviours Scale
Time Frame: prior to the program was implemented and 3 months after the program was implemented
|
Evaluates the extent to which the individual keeps himself active in daily life, regular exercise behaviours and behaviours related to meeting physiological needs such as eating and drinking.
|
prior to the program was implemented and 3 months after the program was implemented
|
|
Scale for Determining Reproductive Health Protective Attitudes of Married Women
Time Frame: prior to the program was implemented and 3 months after the program was implemented
|
It was developed to determine the reproductive health protective attitudes and behaviours of married women.
|
prior to the program was implemented and 3 months after the program was implemented
|
Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- 05/24
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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