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EndometriosisNCT06559852

The Impact of Yoga on Endometriosis-Related Pain

A study testing Yoga in people with Endometriosis, run by Milton S. Hershey Medical Center at 1 site in United States.

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Sites and contacts
Official record

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Trial summary

The central hypothesis of the investigators is that the practice of yoga will result in an improvement of endometriosis related pain symptoms for women with endometriosis. Read more about this study

Who is it for?
Ages 18 to 45 years
Conditions the study is for
Endometriosis
What is being tested?
Yoga
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
15 Oct 2026to 30 Apr 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Reproductive aged women 18-45
  • Self-reported prior surgery with pathology confirming a diagnosis of endometriosis
  • No current use of yoga
  • Baseline moderate pain, score greater than or equal to 5 on VAS scoring
  • Access to internet with wifi capability for zoom platform and completion of weekly surveys
  • Access to items required for yoga session participation (2 blankets or towels, firm pillow, stable chair, wall space, comfortable clothing, water)
  • Ability to commit to duration of 12-week yoga course

Who cannot join

  • Pregnant patients
  • Established yoga participation or moderate exercise regimen
  • Physical trauma or disability
  • Planned surgery or hormonal medication change during study
  • Non-English speaking patients

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site, 1 recruiting
  • Penn State Health

    Hershey, Pennsylvania, 17033

    Ashlie Carter, MD, 7175313503, acarter8@pennstatehealth.psu.edu

    Recruiting

Other trials in United States

About this study

The central hypothesis of the investigators is that the practice of yoga will result in an improvement of endometriosis related pain symptoms for women with endometriosis.

Read the detailed description

Yoga has been demonstrated to improve menstrual pain associated with primary dysmenorrhea through use of physical exercises, mental meditation, and breathing techniques. Still, there has been limited studies assessing potential benefits of yoga on pain symptoms of endometriosis. It is important to further assess yoga as a complementary therapy for women with endometriosis.

Conditions
Endometriosis
Being tested
Yoga
Keywords
Pelvic Pain
Medical subject headings
Endometriosis, Pelvic Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • YogaBehavioural

    Participants will engage in a 12-week virtual yoga course to assess impact on endometriosis-related pain

Study groups in NCT06559852
Study groupRoleWhat they receive
Yoga InterventionExperimentalNot described
Receives: Behavioral: Yoga

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Endometriosis Health Profile-30 Pain Score

    Identify the impact of yoga on endometriosis related pain based on the Endometriosis Health Profile-30, with specific focus on the domain of pain. The EHP-30 questionnaire consists of five scales which includes pain, control and powerlessness, emotional well-being, social support, and self-image and a total of 30 questions. Each scale is translated into a score ranging from 0, or the best health status, to 100, the worst health status.

    Measured: Baseline to completion at 12-weeks

Secondary outcomes (1)
  1. Change in Visual Analog Scale scores

    Comparison of visual analog scale scores from start to the end of the study. The visual analog scale is a validated scale for measuring acute and chronic pain. Scores are recorded on a scale between 0 or "no pain" and 10, the "worst pain".

    Measured: Baseline to completion at 12-weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Aug 2024
  2. Study start15 Oct 2026 (estimated)
  3. Primary completion30 Mar 2027 (estimated)
  4. Study completion30 Apr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06559852
Sponsor's protocol ID
STUDY00025723
Status last verified
Oct 2026
First submitted
15 Aug 2024
Last updated
6 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Plan to publish in an ICMJE journal upon completion of study.

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