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临床试验/NCT04269720
NCT04269720撤回不适用

Impact of a Biofeedback Intervention on Microbiome, Metabolome, and Clinical Outcomes in Pediatric IBD

Ross Maltz0 个研究点开始时间: 2022年9月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
主要终点
Ulcerative Colitis Mucosal healing

研究概览

简要总结

This prospective, randomized, longitudinal, controlled project will occur in two phases. Phase 1 is the pre-diagnosis data collection for treatment-naïve participants who are referred for a diagnostic endoscopy/colonoscopy due to suspicion of IBD. Phase 2 (RCT) is only for patients who are diagnosed with IBD. These patients will be randomized to receive biofeedback intervention daily for 8 weeks or no biofeedback intervention. All participants will receive physician directed standard of care treatment.

详细描述

The inflammatory bowel diseases (IBD), which include Crohn's disease (CD) and ulcerative colitis (UC), affects 3 million Americans. In approximately 25-30% of patients, onset of these chronic diseases occurs prior to the age of 20. Despite medical advances in new therapies, the clinical remission rate on biologics is less than 50% and a significant number of patients will lose response to anti-TNF therapy over time. In addition, patients that require a change in therapy will have a lower response rate to a different biologic. Additional therapies and mechanisms that affect disease activity need to be investigated to identify complimentary treatments that can further impact remission rates without increasing side effects such as lymphoma.

Environmental factors, such as stressor exposure, can exacerbate mucosal inflammation. Patients with IBD report a lower quality of life, as well as increased anxiety and depression. Psychological interventions may improve disease activity. This study will test, using a randomized clinical trial (RCT) design, whether biofeedback intervention will attenuate disease activity. If efficacious, this study will provide a rationale for establishing biofeedback as a complimentary therapy to standard of care to ameliorate stress-induced increases in chronic inflammation.

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
None

入排标准

年龄范围
8 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •The inclusion criteria for Phase 1 are:
  • •Age 8-17 years
  • •Referred for a diagnostic colonoscopy with strong clinical concern for IBD
  • •Live within a 2 hour drive of NCH
  • •There is one additional inclusion criterion for Phase 2:
  • •Patients have been diagnosed with IBD

排除标准

  • •Participants are excluded if they have a comorbid chronic illness, perianal disease, current corticosteroid treatment, taking antibiotics within the last 3 months, psychological disorders that they are undergoing treatment or taking medication for at that time, or undergoing psychological treatments such as cognitive behavioral therapy, mindfulness, or biofeedback therapy at the time of enrollment.
  • •Age and language are limited by the demands of the study (questionnaire completion)

研究组 & 干预措施

Control

No Intervention

Participants will not receive biofeedback intervention.

Biofeedback

Experimental

Participants will receive a biofeedback intervention daily for 8 weeks. Each biofeedback session lasts approximately 10 minutes.

干预措施: Biofeedback (Behavioral)

结局指标

主要结局

Ulcerative Colitis Mucosal healing

时间窗: pre-diagnosis to 12 month follow up

Mayo endoscopic scores for the degree of ulceration. Scores range from 0-3. Higher scores indicate worse inflammation.

Disease activity( Fecal calprotectin)

时间窗: pre diagnosis to 12 month follow up

Fecal calprotectin levels from stool

Crohn's disease mucosal healing

时间窗: pre-diagnosis to 12 month follow up

Simple endoscopic score for CD (SES-CD) scores ileum, right colon, transverse, left colon, and rectum for the degree of ulceration. Scale ranges from 0-3, total score is calculated from sum of all variables for all 5 locations. Scores range from 0-60. Higher scores indicate worse inflammation.

Disease Activity (Crohn's disease)

时间窗: pre diagnosis to 12 month follow up

Pediatric Crohn's Disease Activity Index total score. A standard measure of disease severity that is comprised of information obtained from patient recall (pain severity, stool frequency, limitation of activities), examination (weight, height, abdominal tenderness, perirectal disease, extra- intestinal manifestations), and laboratory data. The Pediatric Crohn's Disease Activity Index total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up. Higher scores indicate more severe disease. Scores range from 0-100.

Disease Activity ( Ulcerative Colitis)

时间窗: pre diagnosis to 12 month follow up

Pediatric Ulcerative Colitis Activity Index total score. A standard Pediatric Ulcerative Colitis Activity Index. a standard measure of disease severity that is comprised pain severity, stool frequency and consistency, rectal bleeding, nocturnal bowel movements, and limitation of activities. The Pediatric Ulcerative Colitis Activity Index total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up. Higher scores indicate more severe disease. Scores range from 0-85.

Stress

时间窗: pre-diagnosis to 12 month follow up

PROMIS Pediatric Psychological Stress Experiences.Scores range from 0-60, with higher scores indicating higher levels of stress.Total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up.

Anxiety

时间窗: pre-diagnosis to 12 month follow up

PROMIS Pediatric Anxiety Short Form. Scores range from 0-60, with higher scores indicating higher levels of anxiety. Total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up.

Pediatric Quality of life

时间窗: pre-diagnosis to 12 month follow up

PedsQL. Scores range from 0-100 with higher scores indicating higher quality of life. Total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up.

Depression

时间窗: pre-diagnosis to 12 month follow up.

Children's Depression Inventory short form. Scores range from 0-54, with higher scores indicating higher levels of depression. Total score will be used from pre-diagnosis, post-intervention, 4 months post-intervention, and 12 month follow up.

次要结局

  • Stress-related changes in the microbiome(pre diagnosis to 12 month follow up)
  • Stress-related changes in the metabolome.(pre diagnosis to 12 month follow up)

研究者

发起方
Ross Maltz
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ross Maltz

Principal Investigator

Nationwide Children's Hospital

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