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临床试验/NCT07087821
NCT07087821招募中不适用

Economic Evaluation of Managing Epilepsy Well (MEW) Network Epilepsy Self-Management Programs

NYU Langone Health4 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2025年9月16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
108
试验地点
4
主要终点
Number of Participants with Patient Health Questionnaire-9 (PHQ-9) Score <5

研究概览

简要总结

The investigators will conduct two-arm randomized controlled trials (RCTs) comparing effects of UPLIFT vs. enhanced usual care and PACES vs. enhanced usual care, respectively, on quality of life, depressive symptoms and seizures over 12 months in NYU patients with epilepsy.

详细描述

UPLIFT and PACES are two evidence-based epilepsy self-management programs whose adoption and impact are limited by the lack of sustainable funding models.

The investigators will conduct an economic evaluation of these programs using data from completed and new trials in both healthcare and community settings.

The investigators will conduct two parallel RCTs to compare effects of UPLIFT vs. enhanced usual care, and separately, PACES vs. enhanced usual care.

Outcome data including patient-reported outcomes and costs will be aligned across the two trials and community implementation and collected at baseline and 3-, 6-, and 12-month follow-up visits for use in the economic evaluations.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults (≥18 years)
  • English-speaking (UPLIFT and PACES) or Spanish-speaking (UPLIFT only).
  • Diagnosed with epilepsy for at least one year
  • Able to understand the informed consent and provide consent
  • Elevated depressive symptoms - Patient Health Questionnaire-9 (PHQ-9) score ≥10; applies to UPLIFT only

排除标准

  • Severe depressive symptoms (score of ≥20 on PHQ-9)
  • Active suicidal ideation (score of ≥1 on PHQ-9 item #9 or otherwise reported during screening)
  • Active psychotic disorder (psychiatric diagnosis and/or antipsychotic medications in the electronic health records (EHR)
  • Significant cognitive impairment (indicated in the EHR or evident during screening)

研究组 & 干预措施

RCT 1: Enhanced Usual Care

Active Comparator

Participants in RCT 1 assigned to the enhanced usual care arm.

干预措施: Enhanced Usual Care (Behavioral)

RCT 1: UPLIFT

Experimental

Participants in RCT 1 assigned to the UPLIFT arm.

干预措施: UPLIFT (Behavioral)

RCT 2: PACES

Experimental

Participants in RCT 2 assigned to the PACES arm.

干预措施: PACES (Behavioral)

RCT 2: Enhanced Usual Care

Active Comparator

Participants in RCT 2 assigned to the enhanced usual care arm.

干预措施: Enhanced Usual Care (Behavioral)

结局指标

主要结局

Number of Participants with Patient Health Questionnaire-9 (PHQ-9) Score <5

时间窗: Baseline

RCT 1 participants only. The PHQ-9 is a 9-item assessment of depression; each item is rated on a scale from 0-3. The total score is the sum of item responses and ranges from 0-27; higher scores indicate greater levels of depression. The primary outcome is the count of participants who score less than 5 on the PHQ-9 (i.e., absence of clinically significant depressive symptoms).

Number of Participants with PHQ-9 Score <5

时间窗: Post-Intervention Month 12 Follow-up (Approximately Month 14)

RCT 1 participants only. The PHQ-9 is a 9-item assessment of depression; each item is rated on a scale from 0-3. The total score is the sum of item responses and ranges from 0-27; higher scores indicate greater levels of depression. The primary outcome is the count of participants who score less than 5 on the PHQ-9 (i.e., absence of clinically significant depressive symptoms).

Composite PHQ-9 and Quality of Life in Epilepsy Inventory-31 (QOLIE-31) Score

时间窗: Post-Intervention Month 3 Follow-up (Approximately Month 5)

RCT 2 participants only. The QOLIE-31 is a 31-item questionnaire evaluating an epilepsy patient's quality of life (QOL) perception. The overall score is derived by weighing and then summing the 7 domain scores, which correspond with the item responses. The overall score is converted to a final, 0-100 point score, where higher converted scores reflect better QOL. The PHQ-9 is a 9-item assessment of depression; each item is rated on a scale from 0-3. The total score is the sum of item responses and ranges from 0-27; higher scores indicate greater levels of depression. The scores from both the PHQ-9 and QOLIE-3 are re-scaled into a combined, Composite PHQ+QOLIE Score ranging from 0-100; higher values indicate more favorable outcomes.

Composite PHQ-9 and QOLIE-31 Score

时间窗: Post-Intervention Month 12 Follow-up (Approximately Month 14)

RCT 2 participants only. The QOLIE-31 is a 31-item questionnaire evaluating an epilepsy patient's quality of life (QOL) perception. The overall score is derived by weighing and then summing the 7 domain scores, which correspond with the item responses. The overall score is converted to a final, 0-100 point score, where higher converted scores reflect better QOL. The PHQ-9 is a 9-item assessment of depression; each item is rated on a scale from 0-3. The total score is the sum of item responses and ranges from 0-27; higher scores indicate greater levels of depression. The scores from both the PHQ-9 and QOLIE-3 are re-scaled into a combined, Composite PHQ+QOLIE Score ranging from 0-100; higher values indicate more favorable outcomes.

5-level EQ-5D version (EQ-5D-5L) Score

时间窗: Baseline

The EQ-5D-5L is a standardized questionnaire used to measure health-related quality of life (HRQoL). It consists of two parts: a descriptive system and a visual analogue scale (EQ VAS). The descriptive system assesses health across five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each with five levels of severity. The EQ VAS provides a self-assessment of overall health on a scale of 0 to 100, where higher scores indicate better health. The EQ-5D-5L will be used to derive utility values to estimate quality-adjusted life years (QALYs) for cost-utility analyses.

EQ-5D-5L Score

时间窗: Post-Intervention Month 12 Follow-up (Approximately Month 14)

The EQ-5D-5L is a standardized questionnaire used to measure health-related quality of life (HRQoL). It consists of two parts: a descriptive system and a visual analogue scale (EQ VAS). The descriptive system assesses health across five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each with five levels of severity. The EQ VAS provides a self-assessment of overall health on a scale of 0 to 100, where higher scores indicate better health. The EQ-5D-5L will be used to derive utility values to estimate quality-adjusted life years (QALYs) for cost-utility analyses.

次要结局

  • Change from Baseline in PHQ-9 Score(Baseline, Post-Intervention Month 12 Follow-up (Approximately Month 14))
  • Change from Baseline in QOLIE-31(Baseline, Post-Intervention Month 12 Follow-up (Approximately Month 14))
  • Change from Baseline in Seizure Frequency(Baseline, Post-Intervention Month 12 Follow-up (Approximately Month 14))
  • Healthcare Utilization(Post-Intervention Month 12 Follow-up (Approximately Month 14))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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