Affiliation:
1. McLean Hospital/Harvard Medical School, Belmont, Massachusetts
2. Department of Medicine Statistics Core, David Geffen School of Medicine at UCLA, Los Angeles, California, USA
Abstract
Abstract
Objective
To evaluate the feasibility, acceptability, and preliminary efficacy of a mind–body intervention for moderate to severe primary dysmenorrhea (PD).
Design
Open trial (single arm).
Setting
Academic medical school.
Subjects
A total of 20 young adult women with moderate to severe primary dysmenorrhea were included across four separate intervention groups.
Methods
All participants received five 90-minute sessions of a mind–body intervention and completed self-report measures of menstrual pain, depression, anxiety, somatization, and pain catastrophizing at baseline, post-treatment, and at one-, two-, three-, and 12-month follow-up. Self-report of medication use and use of skills learned during the intervention were also collected at all follow-up points.
Results
Participants reported significantly lower menstrual pain over time compared with baseline. No changes in anxiety, depression, or somatization were observed, although pain catastrophizing improved over time. Changes in menstrual pain were not associated with changes in medication use or reported use of skills.
Conclusions
A mind–body intervention is a promising nondrug intervention for primary dysmenorrhea, and future research should focus on testing the intervention further as part of a randomized clinical trial.
Funder
National Institute of Child Health and Human Development
UCLA Children’s Discovery and Innovation Institute
National Center for Advancing Translational Sciences UCLA Clinical
Translational Science Institute
Publisher
Oxford University Press (OUP)
Subject
Anesthesiology and Pain Medicine,Clinical Neurology,General Medicine
Cited by
15 articles.
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