- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01115361
Postpartum Family Planning Service Through Enhanced Family Planning in Immunization Services (PPFP-IZ)
Improving Access to and Uptake of Postpartum Family Planning Service Through Enhanced Family Planning in Immunization Services
연구 개요
상세 설명
Study Goal:
To determine the effectiveness of an intervention, which is designed to increase contraceptive prevalence among postpartum women attending vaccination services who desire to either space or limit their pregnancies, thus reducing unmet contraceptive need in this population.
The Intervention:
A. Brief, concise messages conveyed to women during group education sessions regarding pregnancy risk, benefits of FP, and family planning options during the postpartum period.
B.IEC materials such as posters and brochures that deliver messages about the benefits of spacing pregnancies by at least 2 years, LAM, return to fecundity and pregnancy risk during the postpartum period and contraceptive options for postpartum women.
C.Use of a screening tool (Appendix A) to assess pregnancy risk for postpartum women coupled with a brief counseling message depending upon risk classification which includes referral to FP services for those currently or soon-to-be at-risk of pregnancy.
D.Convenient offer of FP services to women attending vaccination services for their infants either concurrently with vaccination services, or at the same facility and on the same day, but at a different time from vaccination services.
Study Design:
Experimental, two-group (intervention/control) pretest (pre-intervention) /posttest (post-intervention) design 12 month intervention period. A mid-course collection of process data will also be conducted at 6 months to assess the degree to which the intervention is being implemented as intended and to provide an opportunity for corrective action if needed.
Participants: Women attending vaccination services for their infants, and vaccination and FP providers
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Kigali, 르완다
- Rwanda health care facilities
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
Clients:
- adult women, aged 21 years and older, or married women ages 18 to 20 who have achieved legal majority status by emancipation due to marriage,
- bring their infants between the ages 6-12 months to immunization services at study sites
Providers:
- all health care providers who currently provide immunization services to infants and/or family planning services within the selected facilities.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 건강 서비스 연구
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: PPFP in child immunization
Women attending immunization services for their infant will receive educational brochures, group education and individual counseling on the benefits of the health timing and spacing of births,, pregnancy risk and return to fertility during the extended postpartum period (12 months), and referral to family planning services for those who are interested.
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A.Group education sessions regarding pregnancy risk, benefits of FP, and family planning options during the postpartum period. B. IEC materials that deliver messages about the benefits of spacing pregnancies by at least 2 years, LAM, return to fecundity and pregnancy risk during the postpartum period and contraceptive options for postpartum women. C. Use of a screening tool to assess pregnancy risk for postpartum women coupled with a brief counseling message and referral to FP services. D.Convenient offer of FP services to women attending vaccination services for their infants. |
간섭 없음: Control - Standard of care
The control arm will receive standard of care infant immunization services.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Use of a modern contraceptive method among postpartum women
기간: 1 year
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The outcome variable is a dichotomous variable - use of modern FP method: yes/no
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1 year
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공동 작업자 및 조사자
스폰서
수사관
- 수석 연구원: Lisa S Dulli, PhD, MHS, FHI 360
- 연구 책임자: Steve Sortijas, MPH, FHI 360
- 수석 연구원: Fidèle Ngabo, MD, MPH, Ministry of Health, Rwanda
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 890028
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. .
Family planning for postpartum women에 대한 임상 시험
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Maureen LyonNational Institute of Mental Health (NIMH)완전한
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Florida State UniversityUniversity of North Carolina, Chapel Hill; University of Georgia초대로 등록
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University of California, Los Angeles모집하지 않고 적극적으로우울증 | 스트레스, 심리적 | 스트레스 장애, 외상성 | 불안 | 부모-자녀 관계 | 육아 | 정서적 스트레스 | 대처 기술 | 감정 조절 | 트라우마, 심리적 | 행동, 어린이미국