Skip to content

Determining the exercise dose required to reduce endometriosis symptoms in regional, rural and remote women.

Determining the exercise dose required to reduce endometriosis symptoms in regional, rural and remote women.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001442493
Enrollment
16
Registered
2025-12-19
Start date
2026-02-16
Completion date
Unknown
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The aim of this study is to examine the critical threshold of differing exercise doses on symptoms, quality of life and biomarkers of endometriosis. It is hypothesized; a larger dose of exercise will result in reductions in symptoms and improvements in quality of life for women with endometriosis in regional, rural and remote Australia,

Interventions

This study will involve a remote 12- week exercise intervention for regional, rural and remote women living with endometriosis. Participants will be allocated into one of four groups: passive control, active control, shorter duration, longer duration. Allocation will be randomized. The intervention is an unsupervised, home-based intervention. Each group will be remotely monitored through their Garmin vivosmart5 watch. Controls: The passive control will involve usual care, the active control gro

This study will involve a remote 12- week exercise intervention for regional, rural and remote women living with endometriosis. Participants will be allocated into one of four groups: passive control, active control, shorter duration, longer duration. Allocation will be randomized. The intervention is an unsupervised, home-based intervention. Each group will be remotely monitored through their Garmin vivosmart5 watch. Controls: The passive control will involve usual care, the active control group will complete 10 minutes of yoga, three times per week for the 12 weeks. The yoga intervention has been designed by the chief investigator, informed by previous research and assessed by three accredited exercise physiologists (AEPs). The chief investigator (Dr Hartmann) is a qualified yoga instructor, and classes will be filmed and made available on an unlisted YouTube channel, Links will be provided upon enrollment into the study. Exercise groups: The shorter and longer duration exercise groups will complete 10 minutes of yoga, three times per week in addition to a walking intervention. The intensity of the walking intervention will be classified as low to moderate (RPE 9-13 on the Borg 6-20) and is self-paced. Adherence will be monitored through the Garmin Vivosmart5 watch. Participants will be encouraged to walk as fast as comfortably possible for 1 minute, every 5 minutes of their sessions. Shorter duration The shorter duration group will commence at 60 minutes total per week (3 x 20-minute sessions), for 6 weeks. After 6 weeks, the duration will be increased to 90 minutes (3 x 30-minutes per week). Longer duration The longer duration group will commence at 120 minutes per week (3 x 40-minute sessions) for 6 weeks. and progress to after 6 week 150 minutes (longer duration group; 3 x 50-minutes per week) respectively, this will be completed for the remaining 6 weeks. Yoga intervention Participants across three groups (active control, shorter and longer duration walking) will complete 10 minutes of yoga, 3 times per week. The yoga classes will involve a series of poses such as child’s pose, cat-cow, gate pose, reclined butterfly, supine twist, low lunge. The yoga intervention incorporates low intensity hatha and yin yoga poses focused on stretching the lower body.

Sponsors

Charles Sturt University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Women (assigned female at birth; AFAB; 18 years and above) with medically diagnosed (imaging/ laparoscopy) endometriosis will be invited to participate. Participants residing in the Modified Monash Model (MMM) areas of MM2-7 will be invited to participate in the study

Exclusion criteria

Participants must not be currently pregnant, breastfeeding or undergoing fertility treatment. Further, participants must not have had pelvic surgery, or an inter-uterine device inserted or removed for the 6 months prior to beginning the study. Moreover, participants who fail the 4-step static balance test, are completing greater than 60 minutes of exercise per week, or are currently using prescription steroids (prednisone or any derivative) will be excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 20, 2026