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临床试验/NCT06184308
NCT06184308已完成不适用

Pilot Clinical Trial of a Home-based Program of Rehabilitation With Health Coaching to Improve Outcomes in Post-intensive Care Syndrome Patients

Mayo Clinic3 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2024年5月8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
发起方
Mayo Clinic
入组人数
78
试验地点
3
主要终点
Completion of home-based rehabilitation program

研究概览

简要总结

The purpose of this study is to gather information on the effectiveness of a home-based rehabilitation program that also includes health coaching in patients who may suffer from post-intensive care syndrome (PICS). Many patients who are admitted to a hospital ICU suffer from new or worsening symptoms related to their medical condition and ICU care. These new or worsening symptoms may persist for some time and are collectively called post-intensive care syndrome (PICS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Supportive Care
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 (age ≥ 18) with PICS defined as admitted to the ICU for more than 48 hours with any of the following conditions: respiratory failure of any cause requiring mechanical ventilation ≥ three days, any shock requiring vasopressors and/or inotropes, development of delirium during the ICU stay, , and cardiac arrest during the index hospital admission.
  • A HABC-M-SR score > 12 points.

排除标准

  • Any mechanical ventilation in the last two months before the index ICU admission
  • ≥ 5 days in the ICU over the previous month before the index ICU admission
  • Receiving hospice or palliative care
  • Severe uncontrolled psychological or psychiatric disorders, e.g., schizophrenia, bipolar disorder, struggling to cope as a result of their personality disorder, uncontrolled substance abuse (alcoholism, illegal drugs) homelessness would make them unsuitable for the intervention
  • A co-morbidity so severe it would prevent the patient from engaging fully in the intervention/ control, e.g., progressive cancer, anoxic brain injury, severe rheumatoid arthritis or osteoarthritis, multiple sclerosis, chronic widespread pain syndrome, previous cerebral vascular event that the patient would not be able to participate in PR
  • Patients with moderate/severe cognitive impairment per medical records screening
  • Inability to obtain informed consent.

研究组 & 干预措施

Piolt (Aim 1) Group: Home-Based Program of Rehabilitation and Health Coaching

Experimental

5-10 subjects will be assigned to complete 20 minutes of Home-based Physical Rehabilitation and Health Coaching for approximately 12 weeks to test feasibility of the home-based rehabilitation program. This will be the initial phase of the study prior to RCT phase.

干预措施: Health Coaching (Behavioral)

Home-Based Program of Rehabilitation and Health Coaching

Experimental

Subjects will complete 20 minutes of Home-based Physical Rehabilitation and Health Coaching for approximately 12 weeks.

干预措施: Home-based Physical Rehabilitation (Behavioral)

Home-Based Program of Rehabilitation and Health Coaching

Experimental

Subjects will complete 20 minutes of Home-based Physical Rehabilitation and Health Coaching for approximately 12 weeks.

干预措施: Health Coaching (Behavioral)

Usual Care

No Intervention

Subjects will receive clinical standard of care.

结局指标

主要结局

Completion of home-based rehabilitation program

时间窗: 12 weeks

Total number of subjects to complete the home-based rehabilitation program per protocol

Change in health related quality of life

时间窗: Baseline, 3 months

Measured by the European Quality of Life 5 Dimensions 5 Level (EQ-5D-5L) score. Questionnaire assess 5 dimensions of health (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) on a 5 level severity scale of no problems, slight problems, moderate problems, severe problems, and unable to perform or extreme problems.

次要结局

  • Change in Anxiety and Depression(Baseline, 3 months)
  • Change in Post-Traumatic Stress Disorder (PTSD) Symptoms(Baseline, 3 months)
  • Change in cognition(Baseline, 3 months)
  • Change in Daily Steps(Baseline, 3 months)
  • Change in Sedentary Time(Baseline, 3 months)
  • Change in Sleep time(Baseline, 3 months)
  • Change in Physical activity(Baseline, 3 months)
  • Healthcare Utilization(3 months)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rodrigo Cartin-Ceba

Principal Investigator

Mayo Clinic

研究点 (3)

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