HASCV-R" Health Programme: a RCT

NCT06439680 | Completed

• 1 other identifier: 05/24
• Study Type: interventional
• Target: 90
• Locations: 1 country
• Sites: 1

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.

Conditions

Health Behavior

Keywords

Health behaviors; health promotion; Women's health

Outcome Measures

Primary Outcomes (1)

• Questionnaire form

  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 Outcomes (2)

• Health Promoting and Protective Behaviours Scale

  prior to the program was implemented and 3 months after the program was implemented

• Scale for Determining Reproductive Health Protective Attitudes of Married Women

  prior to the program was implemented and 3 months after the program was implemented

Study Arms (2)

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.

Other: HASCV-R" Health Programme

control

OTHER

control

Other: HASCV-R" Health Programme

Interventions

HASCV-R" Health Programme OTHER

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

control; experimental

Eligibility Criteria

• Age: 18 Years - 49 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• 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

You may not qualify if:

• 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

Sponsors & Collaborators

• Bozok University: lead

Study Sites (1)

Yozgat Bozok University

Yozgat, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Health Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SEQUENTIAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Phd. Mehmet Korkmaz

Model Details: double-blind randomised controlled pretest-posttest experimental research

Study Record Dates

• First Submitted: May 28, 2024
• First Posted: June 3, 2024
• Study Start: May 15, 2023
• Primary Completion: September 15, 2023
• Study Completion: November 15, 2023
• Last Updated: June 3, 2024

Record last verified: 2023-09

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)