Anxiety Clinical Trial
Official title:
Standardized Yoga & Meditation Program for Stress Reduction for Adolescents With Irritable Bowel Syndrome
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.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | December 15, 2025 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 12 Years to 21 Years |
Eligibility | Inclusion Criteria: - 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 Exclusion Criteria: - Participants under the age of 12 - Participants over the age of 21 |
Country | Name | City | State |
---|---|---|---|
United States | Cooper University Hospital | Camden | New Jersey |
Lead Sponsor | Collaborator |
---|---|
The Cooper Health System |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pediatric Quality of Life | Pediatric Quality of Life Inventory questionnaire will be used | Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks) | |
Primary | Children Somatic Symptoms Inventory | Children Somatic Symptoms Inventory questionnaire will be used | Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks) | |
Primary | Anxiety | Screen for Child Anxiety Related Disorders questionnaire will be used | Change from Pre intervention to 6 weeks after intervention (at completion of intervention which lasts 6 weeks) |
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