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aturopathic Medicine for Endometriosis (NatME) Program: a pilot feasibility trial

Not Applicable
Active, not recruiting
Conditions
Endometriosis
Reproductive Health and Childbirth - Menstruation and menopause
Registration Number
ACTRN12622000222741
Lead Sponsor
Southern Cross University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Active, not recruiting
Sex
Female
Target Recruitment
30
Inclusion Criteria

Patient participants:

1.Aged 18 years or over
2.Female sex
3.Diagnosis of endometriosis made by a medical doctor
4.Intending to seek naturopathic care for the primary purpose of managing endometriosis-related symptoms
5.Speaks fluent English
6.Willing to commit to attending group visits (i.e. cannot foresee a reason for missing two or more sessions)

Practitioner participants:

1.Minimum of 5 years experience in naturopathic clinical practice
2.Currently working as a naturopath in part-time or full-time clinical practice (including casual or locum naturopaths who work at least one day per week).
3.Identify as experienced and having a clinical focus in the area of women’s health and/or endometriosis.
4.Member of an Australian professional association covering naturopaths
5.Holds a Bachelor degree or higher in naturopathy or an Advanced Diploma in Naturopathy completed prior to 2016, as their minimum qualification.
6.Holds professional indemnity insurance that covers the practice of naturopathy
7.Speaks fluent English
8.Must be female

Exclusion Criteria

Patient participants:

1.Seeking naturopathic services solely or primarily for fertility issues, preconception care or pregnancy
2.Women who are pregnant
3.Currently under the care of a naturopath and/or taking herbal or naturopathic medicines
4.Medical diagnosis of serious mental illness (a clinically diagnosed disorder that significantly interferes with an individual’s cognitive, emotional and social abilities, e.g. bipolar disorder or schizophrenia)
5.Active medically diagnosed substance abuse disorder (i.e. alcohol, prescribed or illicit drugs)

Practitioner participants:

1.Male practitioners

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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