RCT of Strategies to Improve Screening Rates Among a Cohort of Cirrhotic Patients at High Risk for Developing HCC in a Safety-net Health System
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,800
- 试验地点
- 2
- 主要终点
- One-time Screening
研究概览
简要总结
Hepatocellular carcinoma (HCC) is the 9th leading cause of cancer-related death in the US and one of the leading causes of death in patients with cirrhosis. Fewer than 1 in 5 high-risk patients undergo HCC screening, with lower rates in non-Caucasian and low socioeconomic status patients receiving care through safety-net health systems. Screening and follow-up failures lead to more advanced cancers, when curative therapies are not available and survival is significantly worse. Over 60% of HCC are diagnosed at advanced stages, due to poor recognition of high-risk patients, underuse of screening among these patients, and poor follow-up of abnormal screening tests. To address these barriers, the investigators propose to conduct a comparative effectiveness research randomized controlled trial of three screening strategies among a socioeconomically disadvantaged and racially diverse cohort of cirrhotic patients at high risk for developing HCC.
Overall, 1800 patients attending Parkland, the Dallas safety-net health system, will be randomized to:
- Group 1: Usual care, with visit-based HCC screening per discretion of individual providers
- Group 2: Mailed HCC screening invitation outreach to eligible patients (low resource intensity)
- Group 3: Mailed HCC screening invitation outreach to eligible patients combined with centralized patient navigation to promote screening completion and follow-up (high resource intensity)
Through three specific aims, this effectiveness research randomized controlled trial will:
- Aim 1: Engage stakeholders in design and implementation of HCC screening outreach interventions.
- Aim 2: Compare the clinical effectiveness and patient acceptability of the intervention strategies to increase completion of one-time and repeat HCC screening.
- Aim 3: Evaluate whether intervention effects are moderated by patient sex, race, ethnicity, English proficiency, and connectedness to primary care.
The screening intervention strategies combine EMR-enabled case identification, system-level screening outreach, and patient navigation to improve identification of previously unrecognized cirrhotic patients, promote HCC screening completion, and facilitate follow-up of abnormal screening tests. This study will engage stakeholders throughout the research process, evaluate the effectiveness and acceptability of HCC screening strategies, and determine which patient subgroups benefit the most.
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
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- 21 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Parkland patients ≥ 21 years of age
- •Diagnosis of cirrhosis or meets criteria for suspected cirrhosis
- •≥ 1 outpatient visit during 12 months prior to randomization
- •Contact information on file
- •English or Spanish speaking
排除标准
- •HCC or suspicious mass on imaging
- •Any malignancy except malignant neoplasm of skin
- •Metastatic solid tumor
- •Palliative care referral
- •Liver transplant
- •Child Pugh C
研究组 & 干预措施
Group 1
Individuals randomized to Group 1 will receive usual medical care and will not be directly contacted at any point of the trial. Study data and outcomes will be abstracted from the EMR.
Group 2
Individuals randomized to Group 2 will receive mailed outreach invitation.
干预措施: Mailed Outreach Invitation (Other)
Group 3
Individuals randomized to Group 3 will receive mailed outreach invitation and patient navigation.
干预措施: Mailed Outreach Invitation and Patient Navigation (Other)
结局指标
主要结局
One-time Screening
时间窗: Outcomes will be adjudicated 6 months after randomization.
Defined as the proportion of patients completing HCC screening within 6 months of randomization.
Repeat Screening (Every 6 Months)
时间窗: Outcomes will be adjudicated 18 months after randomization.
Defined as the proportion of patients completing HCC screening every 6 months within 18 months of randomization.
次要结局
- Repeat Screening (Every 7 Months)(Outcomes will be adjudicated 21 months after randomization.)
- HCC and Early HCC(Outcomes will be adjudicated 18 and 21 months after randomization.)
- Any HCC Screening(Outcomes will be adjudicated 18 and 21 months after randomization.)
- Predictors of HCC Screening Completion(Outcomes will be adjudicated 18 and 21 months after randomization.)
- Intervention Cost(Outcomes will be adjudicated 18 and 21 months after randomization.)
- Proportion of Time Covered(Outcomes will be adjudicated 18 and 21 months after randomization.)
- Suspicious Lesion(Outcomes will be adjudicated 18 and 21 months after randomization.)
研究者
Amit Singal
Professor
University of Texas Southwestern Medical Center
