跳至主要内容
临床试验/NCT05605574
NCT05605574招募中不适用

Longitudinal Early Advance Care Planning Discussions and Documentation (LEADD) Program: An Exploratory Study in Adolescents and Young Adults (AYAs) Receiving Hematopoietic Stem Cell Transplant

National Cancer Institute (NCI)2 个研究点 分布在 1 个国家目标入组 222 人开始时间: 2022年11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
222
试验地点
2
主要终点
Acceptability, Timing of intervention

研究概览

简要总结

Background:

For adolescent and young adults (AYAs) with certain life-threatening illnesses, hematopoietic stem cell transplant (HSCT) provides the best chance for cure and survival. HSCT is a life-saving therapy, but this treatment also comes with significant risks. Given these risks, it is imperative that patients and their families have the opportunity to share their values, priorities, and goals through advance care planning (ACP) to ensure that the care they receive through the transplant process remains patient-centered. Despite the benefits of ACP discussions, many barriers, including provider discomfort, may prevent these conversations with AYAs.

Objective:

To see if AYAs who undergo HSCT and their caregivers benefit from discussing ACP topics.

Eligibility:

People aged 18 to 39 years enrolled in an NIH study with a planned HSCT. One caregiver aged 18 years or older will also be invited to participate.

Design:

Participants will complete a 20-minute questionnaire. They will be asked about the priorities they have related to their care and their prior experiences with ACP.

Participants will have 3 conversations with a study team member over 4 to 9 weeks. Each talk will last 45 to 60 minutes.

First, participants will talk about their upcoming transplant and their expectations. They will also be asked about their fears and worries and will discuss what is most important to them in terms of support, comfort, their values, and their goals.

Next, they will learn about Voicing My CHOiCES . This guide gives people a place to say what kind of care they want to receive during their treatment and includes a place to document how they would want to be cared for if they can no longer make decisions on their own. Participants will be guided as they fill in a few pages from this guide.

The third conversation will review the first talks. Participants may ask questions and review any topic. They will complete follow-up questionnaires and be provided with a summary of their care priorities revealed in the discussions. They will be asked about their experience participating in this study, and their comfort with ACP discussions. They will be asked what they think of the meaningfulness, timing, and cultural sensitivity of these talks....

详细描述

Background:

  • Allogeneic hematopoietic stem cell transplantation (HSCT) carries a significant risk of morbidity and mortality with adolescent and young adult (AYA) patients at inherently high cumulative risk of a myriad of late effects.
  • Participation in advance care planning (ACP) is crucial to promoting patient-centered care and has been shown to have positive impacts on patients, caregivers, and providers. Many barriers exist in the engagement of AYAs and HSCT recipients in ACP conversations, including provider discomfort.
  • A recent retrospective review of AYA patients that received an HSCT at the NIH Clinical Center (CC) in the past 5 years identified patterns of documented ACP discussions. The study revealed that very few patients engaged in ACP discussions beyond completion of an advance directive or physician completion of a medical order. Moreover, the majority of all ACP occurred in patients that ultimately died post-HSCT with most conversations occurring in the last days and weeks of life. Documentation of conversations was scattered throughout many different note types within the electronic medical record.

Objective:

-Assess the feasibility and acceptability of a series of longitudinal conversations about ACP topics with AYA HSCT recipients and their caregivers presenting for HSCT.

Eligibility:

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •INCLUSION CRITERIA:
  • •AYA Participants:
  • •Age >= 18 to <= 39 years.
  • •Planned allogeneic HSCT at a participating site.
  • •Participants must be English speaking.
  • •Ability to understand and the willingness to sign a written informed consent document.
  • •Caregiver Participants:
  • •Age: >= 18 years.
  • •Identified as caregiver by participating AYA participant. Only a single caregiver will be allowed to participate.
  • •Physically present at the participating site.
  • •Participants must be English speaking.
  • •Ability to understand and the willingness to sign a written informed consent document.
  • •Provider participants:
  • •Healthcare providers at the participating site who are part of the AYA participant's HSCT team and provided direct clinical care to AYA participants during period of study enrollment between completion of conversation #1 and conversation #3.

排除标准

  • 未提供

研究组 & 干预措施

1 / Assessments and Conversation

Experimental

Baseline and follow-up assessments and conversations at three timepoints

干预措施: Advance Care Planning conversations (Behavioral)

2 / Survey

No Intervention

Following each AYA/caregiver dyad s completion of timepoint 3, a one-time survey will be sent to a primary clinical attending and APPs who cared for the AYA during the study period

结局指标

主要结局

Acceptability, Timing of intervention

时间窗: Follow-up (Week 4-9)

AYA and caregiver responses to items 2-3 on the ACP Experiences and Comfort Questionnaire; follow-up timepoint ratings of 1-2 on Likert scale (corresponding to agreement that ACP discussions are moderately or extremely important and should occur prior to transplant) reflect acceptability of the timing of the intervention.

Feasibility, Retention

时间窗: Week 9

Target retention rate of 80% of participants for the 8 weeks of the study period (excluding those taken off study due to incapacitation or death).

Acceptability, Emotional impact of intervention

时间窗: Baseline (Week 0), Follow-up (Week 4-9)

AYA and caregiver responses to ACP Experiences and Comfort Questionnaire; mean scores on items (7) and (8) will be compared between baseline and follow up, using paired samples t-tests. Separate chi square analyses will be conducted for sub-items in item (8) to assess if more participants agree (either agree or strongly agree ) or do not agree with the statement at follow-up compared to baseline.

Acceptability, qualitative interview

时间窗: Week 10

Using a grounded theory approach, semi-structured interviews with AYAs and caregivers will be coded and analyzed to explore perceptions of the timing, appropriateness, and meaningfulness of the intervention.

次要结局

  • Concordance of ratings(Baseline (Week 0), Follow-up (Week 4-9))
  • Communication quality(Baseline (Week 0), Follow-up (Week 4-9))
  • Concordance of rankings(Baseline (Week 0), Follow-up (Week 4-9))

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (2)

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