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Intervention for Uterine Fibroids

N/A

Waitlist Available

Research Sponsored by University of Illinois at Urbana-Champaign

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

* The inclusion criteria for the proposed study is any menstruating female with dysmenorrhea, endometriosis, or any menstrual disorder. (Ages 12-65)

Timeline

Screening 3 weeks

Treatment Varies

Follow Up baseline, 3 months, 6 months, 9 months, 12 months

Awards & highlights

No Placebo-Only Group

Summary

This trial is testing if yoga classes can help women with painful or irregular periods feel better. The study focuses on women who have significant pain and discomfort from their menstrual disorders. Yoga is believed to help by promoting relaxation and reducing pain through physical exercises and breathing techniques. Yoga has been shown to alleviate menstrual pain and improve quality of life in women with menstrual disorders.

Eligible Conditions

Uterine Fibroids
Menstrual Disorder
Polycystic Ovary Syndrome
Endometriosis
Dysmenorrhea
Menstrual cramps
Menstrual Pain
Menstrual Cramps

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ baseline, 3 months, 6 months, 9 months, 12 months

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~baseline, 3 months, 6 months, 9 months, 12 months

This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 3 months, 6 months, 9 months, 12 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Menstrual Distress Questionnaire

NIH PROMIS Fatigue Survey

NIH PROMIS Global Health Scale

+4 more

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: InterventionExperimental Treatment1 Intervention

Patients in the intervention group will first undergo 3 months of regular care and then 3 months of biweekly yoga classes. Participants will complete surveys at baseline, 3 months (after of control care), 6 months (after 3 months of biweekly yoga classes), and 12 months (after 6 months of observation and optional yoga practice).

Group II: ControlActive Control1 Intervention

The study lasts 12 months for the intervention and 9 months for the control group with an optional 3 month yoga therapy session offered at the end

0 / 1Eligibility criteria met