跳至主要内容
临床试验/ISRCTN12272130
ISRCTN12272130暂停未知

Comprehensive Anaemia Programme and Personalized Therapies (CAPPT): a non-blinded cluster-randomised controlled trial testing the effect upon haemoglobin in pregnancy of participatory learning and action women’s groups with home-counselling and tailored iron supplementation compared with standard care in southern Nepal.

Health Research and Social Development forum (HERD)0 个研究点目标入组 842 人开始时间: 2021年4月22日最近更新:
适应症

试验速览

阶段
未知
状态
暂停
发起方
入组人数
842

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • Cluster inclusion criteria:
  • 1. Cluster does not adjoin the main East-West which crosses the country Prithivi highway
  • 2. Located in the southern part of Kapilbastu district (closer to the Indian border) where there is low population heterogeneity and low forest coverage
  • 3. Rural area with no major market
  • 4. Populated by predominantly Madhesi (plains ethnicity) population since the burden of anaemia is higher in this group
  • 5. Projected population was =1100 and <3200 (although actual populations were found to be higher when the pre-trial census was conducted)
  • 6. Surrounded by a buffer zone of non-study clusters
  • Menstrual monitoring:
  • 1. Married woman
  • 2. Aged between 13 to 49 years
  • 3. Able to respond to questions
  • 4. Resident of study cluster (whether husband’s or parental home)
  • 5. Husband and women have not had permanent family planning (tubal ligation or vasectomy)
  • 6. Intact uterus (not had hysterectomy)
  • 7. Non-menopausal
  • 8. Has not been told by a doctor that they are infertile
  • 9. Consenting to being asked about menstrual status (to detect pregnancy) once every 4 weeks for up to 7 months
  • For trial enrolment and follow up
  • 1. Same inclusion criteria as for menstrual monitoring (above)
  • 2. Tested positive for pregnancy
  • 3. Less than 20 weeks’ gestation estimated from recall of last menstrual period or uterus not clearly visible above the level of the umbilicus if LMP is not recalled/not available
  • 4. Plans to live in the cluster most of pregnancy or is able to return for counselling and/or data collection
  • 5. Consents to participate in interventions (in intervention arm) and data collection

排除标准

  • 1. Woman is unable to become pregnant (is infertile, has had a hysterectomy, post-menopausal, tubal ligation or husband has had a vasectomy) or does not have a positive pregnancy test
  • 2. Aged <=12 years or >=50 years
  • 3. Not-consenting
  • 4. Unable to respond to questions
  • 5. =20 weeks’ gestation as estimated from LMP (or uterus clearly visible above the level of the umbilicus if LMP is not recalled/not available)
  • 6. Not planning to reside in the study cluster for most of her pregnancy

研究者

发起方
Health Research and Social Development forum (HERD)

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