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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04970420
Other study ID # 0061
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2021
Est. completion date May 2022

Study information

Verified date July 2021
Source Karadeniz Technical University
Contact Ezgi DEMIRTÜRK SELÇUK, MSc
Phone 05448502161
Email demirturkezgi@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: The aims of the research are to determine the effects of individual trainings on family planning given to migrant women (Ahıska Turks), repetitive trainings via mobile applications, telephone counseling initiatives on women's health responsibility levels, family planning knowledge and attitudes. Design: This pretest-posttest is an interventional quasi-experimental research. Method: Standard protocol Items: Recommendations for Interventional Trials (SPIRIT) Statement 2013 checklist is used in this study. The CONSORT (Consolidated Standards of Reporting Trials) flowchart is used in this protocol. This study will be carried out with immigrant (Ahıska Turks) women between the ages of 15-49 who are registered in Üzümlü Family Health Center in Üzümlü district of Erzincan province. In this study, individual training on family planning and health responsibility, repetitive training via mobile application and telephone counseling initiatives will be made. The same applications will be applied to the control group after the study data is collected. Hypotheses: H1: Mobile applications for family planning, telephone counseling and individual training have an impact on the family planning attitudes of immigrant women. H1: Mobile applications for family planning, telephone counseling and individual trainings have an impact on the family planning knowledge level of immigrant women. H1: Mobile applications, telephone counseling and individual trainings for health responsibility have an impact on the level of health responsibility of migrant women.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 86
Est. completion date May 2022
Est. primary completion date October 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 49 Years
Eligibility Inclusion Criteria: - To be registered at the family health center - Being literate - Ability to communicate verbally - Volunteering to participate in the research - Owning a smartphone or a phone belonging to any member of the family that can also be used by the participant - Having internet access at home or at work - Internet use - Able to speak and write Turkish - Being a migrant woman in the age group of 15-49 Exclusion Criteria: - Having a physical or mental health problem - Menopausal, tubal ligation or spouse vasectomy - Inability to reach by phone/visit - Relocation of women to another place - Illness and death of the sampled woman - To have received training on effective family planning

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Health Responsibility and Family Planning in Immigrant Women (Ahiska Turks).
In this study, individual training, training via mobile application and telephone counseling will be given to the experimental group. During the meetings, attention will be paid to the pandemic rules.
Control group
Individual training, mobile application and telephone counseling will be given to the control group after the study data is collected.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Karadeniz Technical University

Outcome

Type Measure Description Time frame Safety issue
Primary Healthy Lifestyle Behaviors Scale II-Health Responsibility Sub-Dimension The lowest score in the Health Responsibility Sub-Dimension was determined as 9 and the highest as 36 points. As the score obtained from the Sub-Dimension of the Scale increases, the health responsibility increases. Health Responsibility sub-dimension Cronbach Alpha coefficient is 0.77. Change in health responsibility at baseline and after 12 weeks.
Primary Family Planning Attitude Scale A minimum of 34 and a maximum of 170 points can be obtained from the scale. The scale has 3 sub-dimensions: "Attitude of the Society towards Family Planning", "Attitude towards Family Planning Methods" and "Attitude towards Birth". Evaluation of the scale is done as individuals with higher scores have more positive family planning attitudes. The internal consistency and homogeneity coefficients determined by the alpha correlations of the scale were found to be 0.90 in total. Change in health responsibility at baseline and after 12 weeks.
Primary Family Planning Information Form This form, which was developed by the researcher based on the literature, consists of questions that include mobile application and telephone counseling comprehensive initiatives. A minimum of 0 and a maximum of 75 points are taken from the form. Evaluation of the form is made as individuals with high scores have knowledge about family planning. Change in health responsibility at baseline and after 12 weeks.
Secondary Family Planning Program Evaluation Form In the form developed by the researchers, it is related to the benefits of the family planning training program for the participants, their satisfaction with the training program, the perception of the knowledge level of women on family planning after the training, suggestions for the development of the training program and the family planning method used after the training. There are 7 questions. Level of satisfaction with the programs implemented after 12 weeks
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