HASCV-R" Health Programme: a RCT

NCT ID: NCT06439680

Last Updated: 2024-06-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-05-15
• Study Completion Date: 2023-11-15

Brief Summary

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.

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.

Conditions

Health Behavior

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

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.

Group Type: EXPERIMENTAL

HASCV-R" Health Programme

Intervention Type: OTHER

HASCV-R program "Healthy nutrition, Active life, Ways to cope with Stress, Cancer and cancer screening, Vaccination - Reproductive health" Training programme

control

control

Group Type: OTHER

HASCV-R" Health Programme

Intervention Type: OTHER

HASCV-R program "Healthy nutrition, Active life, Ways to cope with Stress, Cancer and cancer screening, Vaccination - Reproductive health" Training programme

Interventions

HASCV-R" Health Programme

HASCV-R program "Healthy nutrition, Active life, Ways to cope with Stress, Cancer and cancer screening, Vaccination - Reproductive health" Training programme

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 49 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Bozok University

OTHER

Sponsor Role: lead

Responsible Party

Mehmet KORKMAZ

Phd. Mehmet Korkmaz

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Yozgat Bozok University

Yozgat, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

05/24

Identifier Type: -

Identifier Source: org_study_id