跳至主要内容
临床试验/NCT06512597
NCT06512597招募中不适用

Combination Therapy of Resilience Intervention With Biologics in Crohn's Disease (CATHARSIS Trial)

Icahn School of Medicine at Mount Sinai3 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2024年11月1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
170
试验地点
3
主要终点
The PROMIS Global Health Scale

研究概览

简要总结

People living with Crohn's disease (CD) experience psychological and emotional symptoms, in addition to known chronic and disabling physical symptoms, which prevent them from living their life to the fullest (flourishing). Depression and anxiety are experienced by 30% of people living with CD and 60% of inflammatory bowel disease (IBD) patients continue to report chronic pain, stress, sleeplessness, and fatigue, even when they are "objectively" in remission. Psychological stress has been endorsed by 70% of patients with IBD as a key trigger for disease activity which is not surprising given the significance of the gut-brain-microbiome axis, the close communication between the enteric and autonomic nervous systems, and the role of the hypothalamic-pituitary axis and its neuroendocrine and immune functions in the expression of GI symptoms. Interestingly, up to 85% of patients with CD also endorse the positive impact of effective coping skills on disease course. The PI's prior work has suggested that early provision of effective coping strategies, offered at the time of diagnosis or more precisely, immediately prior to biologic medication initiation, could potentially result in faster healing and improved well-being, likely through the combination of 1) physiological mitigation of the stress response and optimization of the gut-brain-microbiome axis; and 2) promotion of effective coping and disease self-management behaviors that promote psychological flourishing despite disease. Unfortunately, to date, early effective psychosocial care has been limited by concerns over reimbursement for psychological services, access to qualified IBD mental health professionals, and the lack of a standardized methodology focused on the brain-gut stress response and how to assess, monitor, communicate and maintain tight control over both physical and emotional well-being. CATHARSIS is a rigorous, placebo-controlled, randomized controlled trial of coping strategies plus medication for 170 people living with Crohn's for less than 5 years who are about to start a new biologic medication due to active disease. Outcomes include improvements in emotional well-being as well as clinical and endoscopic remission over a 12-month period. The overall goal of the study is to demonstrate that it is essential to combine biologic therapy and psychosocial care to ensure optimal and long-term positive outcomes in CD.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults (18-65 years old) of any sex, gender, and racial/ethnic background with an endoscopically and histologically confirmed CD diagnosis will be eligible.
  • •Participants must have active CD symptoms as defined by a Crohn's Disease Activity Index (CDAI) of at least 220 and
  • •Active endoscopic inflammation defined as a Simple Endoscopic Score for CD (SES-CD) > 6 (or ≥4 for isolated ileal disease) on most recent colonoscopy OR active disease on imaging study OR elevated calprotectin/CRP levels
  • •Must be planning to start an anti-TNF (adalimumab, certolizumab, or infliximab) or anti-IL-23 (risankizumab, guselkumab, mirikizumab) within the prior 2 weeks or in the next 6 weeks.
  • •Participants will need to live in one of Dr Keefer's 30+ PSYPACT licensed states.

排除标准

  • •Endoscopically inactive Crohn's disease at baseline.
  • •Unable to consent to participation.
  • •Pregnant or planning to become pregnant in next 12 months.
  • •Severe psychiatric symptoms.
  • •Surgical history for CD.

研究组 & 干预措施

Time and Attention Control Group - IBD Support Program (Standard Therapy)

Sham Comparator

This 7-session condition will serve as a Time and Attention Control to the Coping Strategies Program. The therapist will follow Dr. Keefer's previously validated control condition manual focused on supportive listening, disease education and self-reflection.

干预措施: Time and Attention Control - IBD Support Program (Behavioral)

Primary Intervention for Combination Therapy - IBD Coping Strategies Program

Experimental

This 7-session protocol is based on Dr. Keefer's validated Project Management for Crohn's disease treatment manual. The program specifically focuses on reducing stress, building resilience, fostering self-confidence and disease acceptance, all of which have been associated with improved adjustment to disease and better self-management outcomes in CD.

干预措施: Primary Intervention for Combination Therapy - IBD Coping Strategies Program (Behavioral)

结局指标

主要结局

The PROMIS Global Health Scale

时间窗: at week 24

Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health Scale A series of person-centered measures that evaluate and monitor physical, mental, and social health in adults and children. 10-item patient-reported questionnaire. standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.

次要结局

  • Simple Endoscopic Score for Crohn's Disease (SES-CD)(at 24 weeks)
  • Patient-Reported Outcomes (PRO2)(at weeks 12, 24, 36, and 52)
  • Psychological Well-Being Scale(at weeks 12, 24, 36 and 52)
  • Inflammatory Bowel Disease Self-Efficacy Scale (IBD-SES)(at weeks 12, 24, 36 and 52)
  • Inflammatory Bowel Disease Questionnaire (IBDQ)(at weeks 12, 24, 36, and 52)
  • UCLA GI Symptom Severity Score(at weeks 12, 24, 36, and 52)
  • Crohn's Disease Activity Index (CDAI)(at weeks 12, 36, and 52)
  • NIH PROMIS-29(at weeks 12, 24, 36 and 52)
  • C-reactive protein level(up to 24 weeks)
  • fecal calprotectin level(up to 24 weeks)

研究者

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

Laurie Keefer

Professor

Icahn School of Medicine at Mount Sinai

研究点 (3)

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