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临床试验/NCT07177170
NCT07177170招募中不适用

Optimizing Cervical Cancer Screening Strategies With HPV Testing Among Women Living With HIV in Cameroon: Feasibility, Acceptability, and Impact of a Single-visit Test and Treat Approach in a Hospital Center With an HPV Testing Platform

Institut de Recherche pour le Developpement1 个研究点 分布在 1 个国家目标入组 1,422 人开始时间: 2024年12月12日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
1,422
试验地点
1
主要终点
Screening completeness

研究概览

简要总结

Context. Cervical cancer (CC) is a leading cause of death among women living with HIV (WLHIV) in resource-limited settings. Yet, effective methods for screening and preventing CC are available. The recommanded approach for CC screening is based on multiple steps, including initial test to detect human papillomavirus (HPV) infection, visual inspection to identify women with HPV at risk for precancerous lesion and treatment when required.

Dropout may occur at these different steps, compromising the success of the CC elimination strategy. Performing the all screening and treatment sequence in a single visit has been recommanded based on the results of a large South African trial. Yet, in many contexts, including those with limited resources, the screening and treatment activities are performed in multiple visites for logistical reasons, resulting in many dropouts. Strategies based on the differentiated prestation approaches, which propose a simplified management centered on the patients preferences, could guide the adaptation of the single-visit approach to account for contextual constraints while maintaining high effectiveness.

The OptiTri-GC study aims to design and assess the impact of a differentiated CC screen and treat strategy in a district hospital; It will assess both its implementation and its effectiveness based on the completeness at each stage of the screening cascade. In addition, it will also include three sub-studies designed to evaluate :

  • The performance of urinary HPV testing.
  • The performance of different methods to identify women requiring a treatment.
  • The risk of post-treatment cervical disease.

This study has two periods. During the first period, a single visit approach will be used while differentiated approach will be prepared using participatory research. During the second period, the differentiated approach will be implemented. The screening overall completeness will be compared between the two periods to assess the differentiated approach effectiveness.

The study will also assess the implementation of each screening strategy in terms of :

  • Success through the measure of fidelity, reach and completeness
  • Identification of adaptation, barriers and facilitating/leverage factors
  • Perception, feasibility and acceptability of the screening strategies (by patients and health care workers) It will assess the participants' stress levels during the screening process and to identify potential psychosocial support strategies and document the experience of WLHIV and health workers during the screening process and the post-treatment follow-up.

Other study objectives include :

  • To assess the performance of different methods to identify women requiring a treatment
  • To assess the performance of HPV testing on a urine sample compared with vaginal self-collected or cervical (clinician-collected) samples
  • To assess the efficacy of treatment in terms of post-treatment cervical lesions

Methodology. Participants will be WLHIV aged 25 to 49 and eligible for CC screening. Health care workers will also be invited to participate to the implementation research. The data collected will be quantitative and qualitative.

详细描述

Context. Cervical cancer (CC) is a leading cause of death among women living with HIV (WLHIV) in resource-limited settings. There is compelling evidence that screening for human papillomavirus (HPV) infection by testing is a very sensitive method for identifying women at risk for precancerous lesions of the cervix. But since HPV infections are very common among WLHIV, it is necessary to have secondary triage to identify women who need to be treated.

The HPV-based screening approach includes multiple steps, and dropout may occur at these different steps, compromising the success of the CC elimination strategy. A single-visit screen and treat approach has been recommanded based on the results of a large South African trial. Yet, in many contexts, including those with limited resources, the screening and treatment activities are often performed in multiple visites for logistical reasons, resulting in many dropouts. Strategies based on the differentiated prestation approach, which propose a simplified management centered on the patients preferences, could guide the adaptation of the single-visit approach to account for contextual constraints while maintaining high effectiveness.

The OptiTri-GC study aims to design and assess the impact of a differentiated CC screen and treat strategy in a district hospital; It will assess both its implementation and its effectiveness based on the completeness at each stage of the screening cascade. In addition, it will also include three sub-studies designed to evaluate :

  • the performance of urinary HPV testing.
  • the performance of different post-HPV test triage options (partial genotyping, simple or Artifical Intelligence assisted visual inspection, methylation markers)
  • the risk of post-treatment cervical disease and the performance of different cure markers.

This will be a type 2 hybrid study that combines intervention research and implementation research. A quasi-experimental design ("before - after") combined with case study will be used for the effectiveness component of the research. During the first period, a single visit approach will be used while differentiated approach will be prepared using participatory research. During the second period, the differentiated approach will be implemented.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Screening
盲法
None

入排标准

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

入选标准

  • HIV infection
  • receiving antiretroviral therapy
  • living in the department of the study hospital

排除标准

  • ongoing pregnancy
  • hysterectomy
  • treatment of cervical lesion in the past 12 months
  • Expected follow-up difficulties: planned absence that could interfere with the participation in the study (e.g., travel abroad, relocation, imminent transfer, etc.);
  • Any pathology or concomitant treatment which, in the opinion of the investigators, contraindicates participation or prevents satisfactory participation in the study Inclusion deferred if
  • menstrual bleeding
  • post-partum (<12 weeks after delivery)
  • clinicla signs of cervical or pelvic infection

结局指标

主要结局

Screening completeness

时间窗: 60 days post screening initiation

Proportion of HPV+ participants completing all screening steps within 60 days of inclusion.

次要结局

  • Screening completeness 2(120 days post screening initiation)
  • Acceptability of the screening delivery strategy(Baseline (screening))
  • Triage performance(Baseline (screening))
  • Performance of urinary HPV test(Baseline (screeening))
  • Post treatment cervical lesion(12 months)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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