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临床试验/NCT03255941
NCT03255941已完成早期 1 期

'A Randomized Controlled Trial of Safety and Effectiveness of Depo Provera Intramuscular and Subcutaneous Administration Comparing Lay Lady Health Workers With Clinically-trained Family Welfare Workers in Pakistan

FHI 3601 个研究点 分布在 1 个国家目标入组 460 人开始时间: 2018年3月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
FHI 360
入组人数
460
试验地点
1
主要终点
Number of Participants That Were Appropriately Screened for Contraceptive Use

研究概览

简要总结

This is a randomized controlled trial comparing lay Lady Health Workers (Lay Health Workers) with Family Welfare Workers (Clinically- trained Health Workers) on quantitative measures of safety and effectiveness of Depo Provera and Sayana Press provision in a clinic setting. This comparative trial will test the non-inferiority hypothesis that Lady Health Workers are just as competent as clinically-trained Family Welfare Workers in screening and counseling first-time injectable users. These first time users will also be randomly assigned to receive intramuscular or subcutaneous injections of DMPA.

详细描述

FHI 360 and Jhpiego in collaboration with USAID, Aga Khan University (AKU) and the Government of Sindh province propose a randomized controlled trial (RCT) to provide evidence that could change current policies in Pakistan that forbid initiation of DMPA by Lady Health Workers (LHWs). Positive findings on the safety and effectiveness of LHW-initiation of DMPA may also prompt the WHO to consider modifying the recommendation for targeted M&E for lay health worker provision of intramuscular injectable contraceptives. The trial will compare the screening and counseling of (LHWs)-the main lay health worker cadre--with that of Family Welfare Workers (FWWs) who are clinically-trained. The Government of Sindh province also expressed interest in introducing Pfizer's subcutaneous form of Depo Provera, Sayana Press® (SP) in Pakistan, which could simplify administration of injectable contraceptives. As such, an SP arm will be included in the trial, which will be facilitated by relevant training of LHWs and FWWs by Jhpiego and stocks provided by a special USAID procurement, since the registration process for SP in Pakistan is ongoing. A successful RCT demonstrating the non-inferiority of LHWs vis á vis FWWs on first-dose initiation of Depo Provera IM (DMPA IM) and (SP) would facilitate efforts to expand CBA2I in Pakistan, and in turn improve access to family planning services for a potentially large number of underserved women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
15 Years 至 49 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Women who voluntarily accept DMPA

排除标准

  • Women unable to provide informed consent
  • Women with contraindications to DMPA
  • Women who are pregnant

研究组 & 干预措施

Clinic Provider - Urban

Active Comparator

Urban Clinic Provider providing DMPA or Sayana Press

干预措施: DMPA (Drug)

Clinic Provider - Urban

Active Comparator

Urban Clinic Provider providing DMPA or Sayana Press

干预措施: Sayana Press (Drug)

Lay Provider - Urban

Active Comparator

Urban Lay Provider providing DMPA or Sayana Press

干预措施: DMPA (Drug)

Lay Provider - Urban

Active Comparator

Urban Lay Provider providing DMPA or Sayana Press

干预措施: Sayana Press (Drug)

Clinic Provider- Rural

Active Comparator

Rural Clinic Provider providing DMPA or Sayana Press

干预措施: DMPA (Drug)

Clinic Provider- Rural

Active Comparator

Rural Clinic Provider providing DMPA or Sayana Press

干预措施: Sayana Press (Drug)

Lay Provider- Rural

Active Comparator

Rural Lay Provider providing DMPA or Sayana Press

干预措施: DMPA (Drug)

Lay Provider- Rural

Active Comparator

Rural Lay Provider providing DMPA or Sayana Press

干预措施: Sayana Press (Drug)

结局指标

主要结局

Number of Participants That Were Appropriately Screened for Contraceptive Use

时间窗: 3 months from randomization

Number of participants that were appropriately screened for injectable contraceptive use in both rural and urban settings in Pakistan.

Number of Participants That Were Appropriately Counseled for DMPA Use.

时间窗: 3 months from randomization

Number of participants that were appropriately counseled by both types of providers in both urban and rural settings.

次要结局

  • Proportion of Clients Who Report Satisfaction With Provider Services(3 months from randomization)
  • Proportion of Clients Providers Who Report Satisfaction With the DMPA Method Received From the Provider(3 months from randomization)

研究者

发起方
FHI 360
申办方类型
Other
责任方
Sponsor

研究点 (1)

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