Ashtangayoga for irritable bowel syndrome in a primary care setting: A feasibility study

Author:

Kern Dorian12ORCID,Lindfors Embla3,Lalér Lisa4,Lindfors Airene5,Ljótsson Brjánn1,Lindfors Perjohan13

Affiliation:

1. Department of Clinical Neuroscience, Division of Psychology Karolinska Institutet Stockholm Sweden

2. Centre for Psychiatry Research Stockholm County Health Care Provision Stockholm Sweden

3. Department of Gastroenterology Akademiska sjukhuset Uppsala Sweden

4. Yogashala Stockholm Sweden

5. Sjöstadsdoktorn Stockholm Sweden

Abstract

AbstractBackgroundIrritable bowel syndrome (IBS) is a common gastrointestinal disorder characterized by diarrhea or constipation and other symptoms such as pain, bloating, and flatulence. The disease often has a negative effect on quality of life and is also associated with symptoms of anxiety and depression. Pharmacological treatments are not always effective, and complementary and alternative treatments are common.MethodsWe conducted a study on a group intervention based on the Ashtanga school of yoga. Fourteen participants (three men, 11 women; average age 51.4, SD = 16) were recruited from primary care, and 10 completed treatment. At pre‐measurement, 4 participants had severe, 9 moderate, and 1 mild IBS, according to the IBS‐SSS scale.Key ResultsThe intervention was regarded as credible (CEQ M = 39.2 SD = 8.8), and no serious adverse events were reported. The intervention showed significant effects on all measurements at post, as follows: IBS‐SSS PRE (M = 272.0 SD = 75.5); IBS‐SSS POST (M = 177.0 SD = 103.5); GSRS‐IBS PRE (M = 48.4 SD = 15.9); GSRS‐IBS POST (M = 37.4 SD = 12.4); VSI PRE (M = 38.8 SD = 10.0) VSI POST (M = 25.9 SD = 10.1); PHQ12 PRE (M = 10.0 SD = 4.3); PHQ12 POST (M = 6.9 SD = 4.3); HADS anxiety PRE (M = 8.9 SD = 5.0) HADS anxiety POST (M = 5.7 SD = 3.3) HADS depression PRE (M = 5.6 SD = 3.2) HADS depression POST (M = 3.8 SD = 2.9) IBS‐QOL PRE (M = 64.5 SD = 12.5) IBS‐QOL POST (M = 72.3 SD = 10.0). The effects were maintained at follow‐up, except for general anxiety and depression. Preliminary effects at 3‐month follow‐up were in the moderate to large range for main outcomes.Conclusion & InferencesA 10‐week group Ashtanga intervention was a feasible intervention for participants with IBS. Preliminary effects were promising and should be explored further in a randomized trial.

Publisher

Wiley

Subject

Gastroenterology,Endocrine and Autonomic Systems,Physiology

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