Skip to main content
. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Am J Obstet Gynecol. 2018 Oct 26;220(1):87.e1–87.e13. doi: 10.1016/j.ajog.2018.10.031

Table 3.

Adverse Events, by Intervention Group

Yoga Group N=28 Control Group N=28 P-valuea
Total number of adverse eventsb reported 23 25 0.77
Number of participants with at least one adverse eventb 17 14 0.59
Total number of adverse events by body/organ system
 Gastrointestinal adverse events 0 2 0.16
 Genitourinary adverse events 1 0 0.32
 Musculoskeletal adverse events 9 8 0.80
 Neurological or psychological adverse events 4 4 1.00
 Ophthalmologic adverse events 1 3 0.32
 Respiratory or sinus adverse events 8 9 0.80
Number of participants with an adverse event by body system
 Gastrointestinal adverse events 0 2 0.16
 Genitourinary adverse events 1 0 0.32
 Musculoskeletal adverse events 8 7 0.80
 Neurological or psychological adverse events 4 4 1.00
 Ophthalmologic adverse events 1 3 0.32
 Respiratory or sinus adverse events 8 9 0.80
Total number of serious adverse eventsc 0 0 1.00
Number of participants with serious adverse eventsc 0 0 1.00
a

P-values for between-group differences in adverse events were calculated from chi-square goodness-of-fit tests.

b

Adverse events were assessed at each study visit or phone call by asking participants to report any negative changes in health since their last visit or call, regardless of relationship to study participation.

c

Serious adverse events were defined by the standard definition of death, life-threatening event, hospitalization, or permanent disability