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临床试验/NCT06270875
NCT06270875已完成不适用

Addressing Pain Through Navigator-Led Palliative Care Optimized for Heart Failure

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年10月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
2
主要终点
Feasibility of Intervention Measure

研究概览

简要总结

Using the MOST framework, factorial pilot design, and an iterative, community-based process, the purpose of this study is to pilot test to further develop and refine a palliative care (PC) intervention addressing pain of Black adults (age > 18) with advanced HF. Thirty-six persons with advancing heart failure (HF) will be randomized to receive one of 16 conditions (different combinations of navigator coach-delivered PC pain intervention components).

详细描述

Developing culturally-responsive, effective, efficient, and scalable and unpacking mechanisms of action of heart failure palliative care interventions have been identified a key research priorities by NIH, AHA, and others. To begin to answer questions of mechanism and efficiency, the study team explored the dose effect of ENABLE CHF-PC, a large phase III RCT that demonstrated small improvements in secondary outcomes of pain intensity and interference. These additional exploratory analyses showed that those with poor baseline QOL and high pain intensity who received a full intervention dose had improved outcomes.

However ENABLE CHF-PC and other HF PC studies included interventions designed to be delivered as a "bundled" package where all intervention participants received the same intervention at set times and dose, making it hard to assess which content or dose led to outcome change. To efficiently test multiple intervention components, doses, and intensity simultaneously requires innovative methods and frameworks, like the Multiphase Optimization Strategy (MOST). Guided by the Total Pain Theory and ENABLE CHF-PC and other HF PC and pain interventions, the project team identified 4 intervention components (HF pain and PC education, relaxation training, COPE attitude and other coping skills, health-related communication) and spirituality and meaning making to be modified, adapted, and evaluated for inclusion in a new, lay navigator-led early palliative care pain telehealth intervention, ADAPT HF (ADdressing pain through A navigator led Palliative care opTimized for Heart Failure).

Aim 1: Using the innovative MOST framework, determine ADAPT HF components feasibility, acceptability, enrollment, retention, and completion rates in advanced HF patients (n=36) for 12 weeks. Feasibility: ≥80% of participants will adhere to and complete assigned intervention components and study-related assessments. Acceptability: Through post-intervention qualitative interviews and acceptability outcomes (acceptability of intervention measure and intervention appropriateness measure), the project team will elicit feedback on intervention components, experiences, and clinical trial procedures.

Aim 2: Explore the preliminary efficacy of ADAPT HF intervention components on outcomes at 12- and 24- weeks after baseline including a) pain interference & pain intensity (primary outcome) using PROMIS measures b) symptom burden using the Edmonton Symptom Assessment Scale and c) mood using the Hospital Anxiety and Depression Scale and d) QOL using the Kansas City Cardiomyopathy Scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Data collectors and principal investigator will be blind to participant condition; participants will be instructed NOT to discuss their assignment with data collectors. Trials participants will know their intervention condition as will the palliative care coach involved in delivering the intervention.

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

  • African American
  • Diagnosis of advanced heart failure (New York Heart Association Class II-IV or American College of Cardiology/American Heart Association Stage C-D)
  • English speaking
  • Willing to participate
  • Primary residence in CAPC East South Central or West South Central regions* (Alabama, Mississippi, Tennessee, Kentucky, Arkansas, Louisiana, Oklahoma, Texas)
  • Self-endorses pain in the last month
  • Willing to participate in intervention and data collection

排除标准

  • Not African American
  • Ineligible HF classification
  • Self-reported, untreated severe mental illness
  • Active Suicidal Ideation
  • Active substance abuse
  • Uncorrected hearing loss
  • Unable to respond in English

研究组 & 干预措施

Coached: Basic pain education + self-care + basic communication & Self-led: spirituality

Experimental

1 telephone weekly session on pain psychoeducation, lay coach-led self-care and relaxation tips, 1 session on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + self-care + basic communication + spirituality

Experimental

1 telephone weekly session on pain psychoeducation, lay coach-led self-care and relaxation tips, 1 session on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + self-care + advanced communication & Self-led: spirituality

Experimental

1 telephone weekly session on pain psychoeducation, lay coach-led self-care and relaxation tips, 2 sessions on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + self-care + advanced communication + spirituality

Experimental

1 telephone weekly session on pain psychoeducation, lay coach-led self-care and relaxation tips, 2 sessions on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + basic communication & Self-led: self-care + spirituality

Experimental

1 telephone weekly session on pain psychoeducation, self-guided self-care and relaxation tips, 1 session on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + basic communication + spirituality & Self-led: self-care

Experimental

1 telephone weekly session on pain psychoeducation, self-guided self-care and relaxation tips, 1 session on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + advanced communication & Self-led: self-care + spirituality

Experimental

1 telephone weekly session on pain psychoeducation, self-guided self-care and relaxation tips, 2 sessions on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: Basic pain education + advanced communication + spirituality & Self-led: self-care

Experimental

1 telephone weekly session on pain psychoeducation, self-guided self-care and relaxation tips, 2 sessions on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + self-care + basic communication & Self-led: spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, lay coach-led self-care and relaxation tips, 1 session on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + self-care + basic communication + spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, lay coach-led self-care and relaxation tips, 1 session on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + self-care + advanced communication & Self-led: spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, lay coach-led self-care and relaxation tips, 2 sessions on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + self-care + advanced communication + spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, lay coach-led self-care and relaxation tips, 2 sessions on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + basic communication & Self-led: self-care+ spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, self-guided self-care and relaxation tips, 1 session on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + basic communication + spirituality & Self-led: self-care

Experimental

2 telephone weekly sessions on pain psychoeducation, self-guided self-care and relaxation tips, 1 session on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + advanced communication & Self-led: self-care+ spirituality

Experimental

2 telephone weekly sessions on pain psychoeducation, self-guided self-care and relaxation tips, 2 sessions on social support and communication coaching, self-guided spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

Coached: advanced pain education + advanced communication + spirituality & Self-led: self-care

Experimental

2 telephone weekly sessions on pain psychoeducation, self-guided self-care and relaxation tips, 2 sessions on social support and communication coaching, coach-led spirituality and meaning coping

干预措施: ADAPT HF (Behavioral)

结局指标

主要结局

Feasibility of Intervention Measure

时间窗: 12 weeks

A 4-items scale that measures implementation outcomes that are often considered "leading indicators" of implementation success. Minimum score is 4 and maximum score is 20. Higher scores indicated higher feasibility and lower scores indicate less feasibility.

PROMIS Pain Intensity Scale

时间窗: Baseline and 12 weeks

Through PROMIS measures, we will explore reports on pain intensity. This includes a 3-item questionnaire on pain intensity and a 6-item question on pain interference over a week. Minimum score is 3 and the maximum score is 15. Higher values indicate higher pain intensity. Lower values indicate lower pain intensity.

Acceptability of Intervention Measure (AIM)

时间窗: 12 weeks

A 4-item measure of perceived intervention acceptability. Items are measured on a 5-point Likert scale (Completely Disagree-Completely Agree). Minimum score is 4 and maximum is 20. Higher scores indicate a higher chance of acceptability. Lower scores indicate a lower chance of acceptability.

Pain Interference Scale Short Form 6b

时间窗: Baseline and 12 weeks

A 6-item self-reported measure of the consequences of pain on relevant aspects of a person's life and may include the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. Minimum score is 6 and maximum score is 30. Higher scores indicate higher pain interference. Lower scores indicate lower pain interference.

Feasibility of Intervention Delivery and Data Collection

时间窗: Baseline and 12 weeks

Proportion of participants who complete assigned intervention components and study-related assessments.

次要结局

  • PROMIS General Self-efficacy(Baseline & 12 weeks)
  • Self-care of Heart Failure Index(Baseline & 12 weeks)
  • Hospital Anxiety and Depression Scale (HADS)(Baseline and 12 weeks)
  • Multidimensional Scale of Perceived Social Support (MSPSS)(Baseline & 12 weeks)
  • SF Global Health Scale(Baseline & 12 weeks)
  • Edmonton Symptom Assessment Scale (ESES-r)(Baseline and 12 weeks)
  • Kansas City Cardiomyopathy Questionnaire- Short Form(Baseline and 12 weeks)
  • Patient Activation Measure (PAM) Short Form(Baseline & 12 weeks)
  • Connor-Davidson Resilience Scale (CD-RISC-10)(Baseline & 12 weeks)
  • Cost/Resource Utilization Form(Baseline & 12 weeks)
  • Brief Multidimensional Measure of Religiousness / Spirituality (BMMRS) - 6-item subscale for Religious/Spiritual Coping + 1 overall Q(Baseline & 12 weeks)
  • Discrimination in Medical Settings Scale Scale(Baseline & 12 weeks)

研究者

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

Rachel Wells

Assistant Professor

University of Alabama at Birmingham

研究点 (2)

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