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临床试验/NCT05719246
NCT05719246招募中不适用

Standardized Yoga & Meditation Program for Stress Reduction for Adolescents With Irritable Bowel Syndrome

The Cooper Health System1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2020年12月30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
10
试验地点
1
主要终点
Pediatric Quality of Life

研究概览

简要总结

Irritable Bowel Syndrome (IBS) is the most common cause of recurrent abdominal pain in children. IBS is a functional gastrointestinal disorder that is linked to motor and sensory physiology, as well as the central nervous system, that presents as abdominal pain with abnormal defecation patterns. This discomfort leads to emotional stress, decreased quality of life, and anxiety. The study proposes that yoga and mindfulness will decrease anxiety and increase quality of life for patients with IBS. The aim of this study is to measure the impact of a brief, at-home, 6-week twice per week Standardized Yoga & Meditation Program for Stress Reduction program on anxiety, IBS symptoms, and quality of life in children ages 12-21 diagnosed with IBS.

详细描述

Background: Irritable Bowel Syndrome (IBS), is the most common cause of general recurrent abdominal pain (RAP) in children. IBS is a functional gastrointestinal disorder that is linked to motor and sensory physiology, as well as the central nervous system, that presents as abdominal pain with abnormal defecation patterns. This discomfort often significantly impacts the patient's life, leading to emotional stress, decreased quality of life due to necessary changes in daily living to accommodate bathroom patterns, as well as anxiety and depression. Since IBS is often accompanied by anxiety, along with other psychological and quality of life issues, it will be evaluated whether practicing yoga and mindfulness will decrease anxiety and increase quality of life for patients with IBS

Objective

To measure the impact of a brief, at-home, 6-week twice per week Standardized Yoga & Meditation Program for Stress Reduction (SYMPro-SR) program on anxiety, IBS symptoms, and quality of life in children ages 12-21 years old diagnosed with Irritable Bowel Syndrome.

Methods: This is a pilot, IRB approved, prospective study. Children ages 12-21 who suffer from any of the four types of Irritable Bowel Syndromes will be identified. Each subject will be asked to fill out the Screen for Child Anxiety Related Disorders, Children Somatic Symptoms Inventory and Pediatric Quality of Life Inventory questionnaires before and after an online, 6- week yoga course. Anxiety will be measured using the Screen for Child Anxiety Related Disorders and quality of life will be measured using Pediatric Quality of Life Inventory and Children Somatic Symptoms Inventory tests. Results of the questionnaires total scores and sub-scales will be analyzed as continuous variables using paired t-tests or the Wilcoxon signed rank tests for the pre-post results and ANCOVA for repeated measures incorporating age, sex, baseline scores, etc. as covariates. Comparisons within the group will be done using Student paired t-test for continuous data. The difference will be considered significant at p<0.05.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
12 Years 至 21 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients of Cooper Pediatric Gastroenterology practice in Camden, NJ or Voorhees, NJ
  • •Patients of Cooper Pediatric Gastroenterology practice in Voorhees, NJ
  • •Participants 12 to 21 years old with any type of IBS diagnosis
  • •Subjects must be able to access the internet to be able to watch the yoga videos on Youtube
  • •Patients must complete 4 out of 6 modules to stay in the study

排除标准

  • •Participants under the age of 12
  • •Participants over the age of 21

研究组 & 干预措施

IBS Patients Doing Yoga

Experimental

All patients will fall under the arm of "IBS Patients Doing Yoga" and will follow the yoga videos that are assigned to them during the study. The participants are their own controls and their symptom changes will be recorded pre- and post-video watching and participation.

干预措施: Yoga (Behavioral)

结局指标

主要结局

Pediatric Quality of Life

时间窗: Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks)

Pediatric Quality of Life Inventory questionnaire will be used

Children Somatic Symptoms Inventory

时间窗: Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks)

Children Somatic Symptoms Inventory questionnaire will be used

Anxiety

时间窗: Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks)

Screen for Child Anxiety Related Disorders questionnaire will be used

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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