- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04970420
Health Responsibility and Family Planning ın Immigrant Women (Ahıska Turks). (HeRFAPIW)
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.
연구 개요
상태
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Ezgi DEMİRTÜRK SELÇUK, MSc
- 전화번호: 05448502161
- 이메일: demirturkezgi@gmail.com
연구 연락처 백업
- 이름: Birsel Canan DEMİRBAĞ, PhD
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
---|---|
활성 비교기: 대조군
|
Individual training, mobile application and telephone counseling will be given to the control group after the study data is collected.
|
실험적: HeRFAPIW
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.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Healthy Lifestyle Behaviors Scale II-Health Responsibility Sub-Dimension
기간: 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
기간: 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
기간: 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.
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Family Planning Program Evaluation Form
기간: 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
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (예상)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
- 0061
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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