跳至主要内容
临床试验/NCT07209917
NCT07209917招募中不适用

Secondary Cervical Cancer Prevention of Vulnerable Women With Human Papillomavirus (HPV) and Human Immunodeficiency Virus (HIV) Co-infection in India

University of California, Irvine5 个研究点 分布在 1 个国家目标入组 348 人开始时间: 2026年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
348
试验地点
5
主要终点
HR-HPV Detection

研究概览

简要总结

Cervical cancer (CC) remains one of the most common malignancies among women in India, with nearly 100,000 women diagnosed annually and over 60,000 preventable deaths annually. With high-risk human papillomavirus (HR-HPV) as the causative agent for CC, one risk factor that places women at high risk for CC is human immunodeficiency virus (HIV), as impaired immune response against Human papillomavirus (HPV) may result in persistent HR-HPV infection, a critical risk factor for progression of HPV-related cervical oncogenesis. Progression of precancerous lesions among women living with HIV (WLH) is also associated with: 1) lack of HPV screening; 2) high levels of depressive symptoms and stigma; and 3) malnutrition, which negatively impacts the activation and proliferation of immune cells. Yet programs that offer WLH with comprehensive services focused on HPV screening and psychological and nutritional support are almost non-existent, and the gap is critical. Nutrition plays an integral role in relationship to HPV/HIV co-infection, as demonstrated by an increased risk of HR-HPV associated with poor nutrition; nutritional deficiencies are likewise linked to cervical intra-epithelial neoplasia. The immunological effect of malnutrition may also be exacerbated among WLH due to elevated energy demands of chronic immune activation; worsened with HPV/HIV co-infection. Further, depressive symptoms (aka depression for brevity) partially mediate the effect of food insecurity on HIV viral suppression. In our completed ASHA-Nutrition R01 study of antiretroviral (ART) adherence, the investigators trained lay community health peer counselors, named Accredited Social Health Activist (ASHA), to improve the health of 600 rural WLH by providing emotional support, skill-building, nutrition education, and/or protein-enriched food supplements. In that study, our intervention, co-delivered by our trained peer counselors, and guided by nurses, led to increased CD4+ T cell recovery and improved anthropometric and psychosocial outcomes. The investigators found that peer counselors support plus protein supplements and nutritional education were significantly associated with improved CD4 counts and increased lean mass at 18 months (P < 0.001), as well as significant improvements in depression, ART adherence, social support and internalized stigma. In our sub study, CC screening of 598 of these WLH revealed that 13% were found to have abnormal cervical lesions and 4 (1%) had squamous CC. Preliminary evidence also revealed that nutritional supplements may be associated with a 40% reduction in the risk of abnormal cervical lesions (adjusted odds ratio [aOR] = 0.60), with an association between serum albumin and reduced risk of abnormal lesions (aOR= 0.39).

With a focus on secondary prevention of CC, the investigators hope to mitigate the link between HR-HPV persistence and risk of CC as well as improve the health of women co-infected with HPV/HIV (W-Co-V). Our stellar team plans to build upon our prior ASHA-Nutrition intervention, using formative research to refine a nurse-led, peer counselors co-delivered, nutrition-enhanced SAKHI HPV intervention, adapted for W-Co-V. This will be followed by a randomized controlled trial (RCT), assessing the efficacy of our refined comprehensive, multifaceted SAKHI HPV intervention, as compared with an enhanced Standard of Care (SOC+) (usual care + 3 sessions [wellness, basic nutrition and HPV/HIV health promotion]) among 348 high-risk co-infected women to prevent CC while remaining engaged in the HIV treatment cascade, and managing nutritional health. Recruited participants will be individually randomized in a 1:1 ratio to one of the two study arms. Our Primary outcome is HR-HPV persistence (2 positive tests for the same HR-HPV type, separated by 12-18 months). The two aims incorporating RCT interventions are as follows:

Aim 2. To evaluate the efficacy of SAKHI HPV intervention among 348 W-Co-V on the primary outcome (HR-HPV persistence) as compared to the Enhanced Standard of Care (SOC+) program. H2: Compared to the SOC+ participants, SAKHI participants will have lower rates of HR-HPV persistence.

Aim 3. Assess the impact of the SAKHI program secondarily on: 1) HIV indices (HIV viral load; CD4 count); 2) Nutritional index (serum albumin) at 6-, 12-, and 18-months.

详细描述

In this 5-year parallel-group RCT, the investigators will conduct a RCT to assess the efficacy of our six-month SAKHI HPV intervention, featuring: 1) eight in-depth group education sessions by nurses, OB/GYN and HIV physicians, psychologists, and nutrition experts on HPV/HIV, CC, and nutrition; 2) peer counselor supported 1:1 sessions and community referrals; and 3) selected life skills training by expert artisans as compared to an Enhanced Standard of Care (SOC+) program, featuring 3 group sessions: wellness, basic nutrition and HIV/HPV information and referrals. The primary outcome is HR-HPV persistence (consecutive positivity for same HR-HPV type, separated by 12-18 months).

Secondary outcomes include improved: 1) HIV-related indices (HIV viral load and CD4 count); 2) Nutritional indices (serum albumin) measured at 6, 12, and 18 mos.

The investigators will conduct a two-arm parallel-group RCT among 348 W-Co-V who are cared for at the Belgaum District ART centers. Participants recruited in Karnataka will be individually randomized in a 1:1 ratio to the SAKHI and SOC+ study arms prior to enrollment. A cohort of 16 women (8 per group) will be enrolled every month. Primary outcome, HR-HPV persistence (positivity for same HR-HPV type, separated by 12-18 months), will be compared to enhanced standard of care (SOC+) control group that is above and beyond what is typically offered to WLH treated in the health facility. Persistent HR-HPV is a widely used outcome for HPV vaccine and other CC prevention interventions, due to its critical role in HPV-related cervical oncogenesis. Secondary outcomes will focus on improvement in: 1) HIV related indices (HIV viral load and CD4 count); and 2) Nutritional index, serum albumin levels - a marker for protein consumption).

Setting: Karnataka is selected as our key site for the study as rates of HPV have remained second highest in the country. The W-Co-V are being recruited from underserved ART centers in the Bangalore and its surrounding districts. In the next several months, the team will be in Districts outside Bangalore including Tumkur, and Kolar, while additional sites will be conducted in Northern Karnataka to include Belgaum, Athani, Chikooi, Gokak, Raibagh and Saudatti.

The KSAPS (Karnataka State acquired immunodeficiency syndrome (AIDS) Program Society) has approved these sites to participate in our study. To enroll 348 W-Co-V, a total of 3480 WLH will be screened; thus, ongoing screening of our staff will be conducted in all ART centers. First-line ART is offered free by the government to all eligible PLWH and all newly diagnosed are referred to the ART centers. Thus, the investigators anticipate the 6 ART Centers will provide a sufficient number of eligible women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Care Provider, Outcomes Assessor)

入排标准

年龄范围
25 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • WLH, 25 - 50 years of age; based on HIV-based guidelines;
  • Receiving ART for > 12 months to ensure medication stabilization, and ensure any impact on the cervical cancer outcomes will not be attributed solely to recent ART initiation, as validated by an ART card given to all ART patients;
  • Screened as HPV positive by RT-PCR (Reverse Transcription Polymerase Chain Reaction) for oncogenic genes; and assessed to be VIA negative;
  • Have not participated in Phase I Formative Study.

排除标准

  • Pregnant or lactating women due to hormonal and dietary guideline differences;
  • Women older than age 50 These women will be immediately referred to a gynecology specialist.

研究组 & 干预措施

SAKHI HPV Intervention

Experimental

The SAKHI program will include: 1) 8 group sessions, led by the nurse, and inclusive of other experts (such as HPV/HIV physician, nutritionist, psychologist) to provide the group classes for each cohort of 8 W-Co-V in the program, covering content about staying healthy, taking care of self/family, skills building, and eating healthy; 2) Individual 1:1 weekly peer counselor support; and 3) referral to grant-supported life skills classes taught by experts.

干预措施: SAKHI HPV Intervention (Behavioral)

SOC+

Other

The investigators will offer an enhanced standard of care to include usual care + three (1.5 hour) group sessions on wellness, basic nutrition, coping with mental health issues, importance of HPV screening and treatment as needed, and ART adherence (similar to Modules for SAKHI), and similarly delivered by the nurse and content experts over the six-month intervention.

干预措施: Enhanced Standard of Care (SOC+) (Behavioral)

结局指标

主要结局

HR-HPV Detection

时间窗: Baseline and month 6, 12 and 18 month follow-ups

HR- HPV test will detect 14 oncogenic HR-HPV genotypes (HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68). HR-HPV persistence is defined as the presence of the same genotype over at least 12 months.

次要结局

  • CD4 Count(Baseline and month 6, 12, and 18)
  • Serum-based Albumin(Baseline and month 6, 12, and 18)
  • HIV Viral Load(Baseline and month 6, 12, and 18)
  • HIV Viral Load(Baseline and month 6, 12, and 18)
  • CD4 Count(Baseline and month 6, 12, and 18)
  • Serum-based Albumin(Baseline and month 6, 12, and 18)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adeline Nyamathi

Distinguished Professor

University of California, Irvine

研究点 (5)

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