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Health Responsibility and Family Planning ın Immigrant Women (Ahıska Turks). (HeRFAPIW)

11. juli 2021 opdateret af: Ezgi Demirtürk Selçuk, Karadeniz Technical University

Evaluation of Nursing Interventions Given to Immigrant Women (Ahıska Turks) Towards Health Responsibility, Family Planning Knowledge and Attitude

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.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

86

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

  • Navn: Birsel Canan DEMİRBAĞ, PhD

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

15 år til 49 år (Barn, Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Kontrolgruppe
Andet: Control group
Individual training, mobile application and telephone counseling will be given to the control group after the study data is collected.
Eksperimentel: HeRFAPIW
Health Responsibility and Family Planning ın Immigrant Women (Ahıska Turks).
Andet: Health Responsibility and Family Planning ın Immigrant Women (Ahıska 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Healthy Lifestyle Behaviors Scale II-Health Responsibility Sub-Dimension
Tidsramme: Change in health responsibility at baseline and after 12 weeks.
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.
Family Planning Attitude Scale
Tidsramme: Change in health responsibility at baseline and after 12 weeks.
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.
Family Planning Information Form
Tidsramme: Change in health responsibility at baseline and after 12 weeks.
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.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Family Planning Program Evaluation Form
Tidsramme: Level of satisfaction with the programs implemented after 12 weeks
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

Samarbejdspartnere og efterforskere

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Sponsor

Karadeniz Technical University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Forventet)

1. juli 2021

Primær færdiggørelse (Forventet)

1. oktober 2021

Studieafslutning (Forventet)

1. maj 2022

Datoer for studieregistrering

Først indsendt

30. juni 2021

Først indsendt, der opfyldte QC-kriterier

11. juli 2021

Først opslået (Faktiske)

21. juli 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

21. juli 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

11. juli 2021

Sidst verificeret

1. juli 2021

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • 0061

Plan for individuelle deltagerdata (IPD)

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