Holistic Medicine Treatment of Uterine Fibroids-Adults (HMTXUFAdult)

January 31, 2026 updated by: Virtual Tribunal Monastery

The Impact of Holistic Medicine Treatment for Bachelorettes Residing on Tribal Lands or in the State of Alaska Living With Uterine Fibroids-1St Diagnosis, Uterine Fibroids Affecting Pregnancy, or Uterine Fibroid Degenerated

This clinical trial aims to evaluate the efficacy of holistic medicine treatments for unmarried women ("Bachelorettes") residing on U.S. Tribal Lands or in the State of Alaska who have been clinically diagnosed with uterine fibroids. The study will assess both primary and secondary outcomes, while accounting for socioeconomic and cultural factors that may influence treatment efficacy and data validity. The research acknowledges the unique sociocultural and economic contexts of Tribal communities and aims to contribute to equitable healthcare research practices, with particular attention to urban poverty, unmarried status, and substance-free lifestyle factors.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Detailed Description

OBJECTIVES:

To evaluate the clinical efficacy of holistic medicine treatments for uterine fibroids among unmarried women on Tribal Lands or in the State of Alaska, with focus on urban and economically disadvantaged populations.

To assess the influence of socioeconomic factors including urban poverty, marital status, and substance-free lifestyle choices on treatment outcomes.

To identify barriers to participation and data validity arising from systemic inequities affecting Tribal communities and urban populations experiencing poverty.

Study Type

Interventional

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Alaska
      • Anchorage, Alaska, United States, 99501
        • Virtual Tribunal Monastery

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria: To join this study, you must meet these simple requirements:

  • Be a Bachelorette Alaska Medicaid recipient age 21 years old and older.
  • Have been told by a doctor that you have uterine fibroids (non-cancerous growths in your uterus).
  • Live on Tribal Lands or anywhere in the State of Alaska,
  • Be willing to try natural, nonclinical holistic treatments alongside regular clinical medical care.
  • Acknowledge smoke-free, drug-free, and alcohol-free church policy
  • Must have access to the internet, Holy Bible (KJV) and a portable fetal Doppler to listen to and monitor uterine fibroid heart rate in spiritual mysteries.
  • Religious or spiritual belief in prayer meditation for faith-based healing.
  • Must agree to medical ethical standards in Greek text pertaining to the Hippocratic Oath.
  • Due to a new tool in the Toolkit: DOGS HELP TO DETECT COVID-19, a negative COVID-19 test may be required at any time whenever COVID-19 is suspected without remedy.

You May Still Qualify Even If:

  • You haven't tried other treatments yet.
  • You're currently receiving other fibroid treatments.
  • You live in a remote area with limited healthcare access.
  • You prefer natural or traditional healing approaches.
  • You have concerns about surgery or medications.

Exclusion Criteria:

  • Noncompliance to Inclusion Criteria.
  • Married relationship status
  • Gender conversion
  • Repeat Offenders
  • Ineligible for Alaska Medicaid
  • Smokers, vapors, alcoholics, drug abusers.
  • Non-Believers in Christian religious practices or prayer.
  • Immobility
  • Diseases without clinical diagnosis, medical treatment, and remedy.
  • Uterine Fibroids premature removal by invasive/noninvasive surgery or Birth Control before climacteric.
  • Unreported violence or abuse can inadvertently influence the validity of this study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Resource Utilization Group (RUG)
nonclinical variables
Behavioral: Holistic Medicine (HM)
With informed consent the participant act as a partner to their health and acknowledges responsibility for self-help or self-care directed activities in a non-clinical setting. Transcendence in research involves actively exploring the best possible options or resources for a resolution or self-determination or hypotheses. To reinforce healthy activities, periodic forecast consist of one or more of the following variables: pastoral counseling, lectures, group discussions, sound therapy, team building exercises, faith-based initiatives, outdoor exercise, walking group, support group, supportive care, cooking class, critical thinking questioning and self-assessment tests. Adult content variables are classified under gender-specific care Respite ( i.e. watch party, gaming, music therapy, interactive Spiritual story, clothing model therapy, portable foot spa and portable foot massage) TO (Time-Out).
Other Names:
  • Holistic Education
  • Transcendence Research
  • Adult Education

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Holistic Medicine Qualitative Method
Time Frame: 1 year
Qualitative data are not expressed numerically. Qualitative evaluation method summarize evidence from instructed methods of data collection relevant to socioeconomic factors, naturalistic observation, and existing records. Hierarchy scales of evaluation determine client wellness stages and identify areas requiring additional nonclinical variables for optimum wellness.
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Holistic Medicine Quantitative Method
Time Frame: 1 year
Based on an average score total 1-100 point scale questionnaire, self-assessment, and/or critique forms will be used to measure socioeconomic factors as well as behaviors, impact, reaction, coping, etc...
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Virtual Tribunal Monastery

Investigators

  • Study Chair: Jones, Humanitarian Veterans Association

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Jones G. Transcendence Research: Counterterrorism to Prevent Victimization. Transcendence Research: Holistic Healthcare for At-Risk Homelessness Pursuant to Chronic Health Conditions. 2025 December; 1(2).
  • Jones G. Transcendence Research: Holistic Healthcare for At-Risk Homelessness Pursuant to Chronic Health Conditions. Transcendence Research. 2025 December; 1(1).
  • Jones G. Transcendence Research: Holistic Healthcare for Social-Welfare Inequities Pursuant to Chronic Health Conditions. Transcendence Research: Holistic Healthcare for At-Risk Homelessness Pursuant to Chronic Health Conditions. 2026 January; 2(1).

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 26, 2026

Primary Completion (Estimated)

January 19, 2029

Study Completion (Estimated)

January 19, 2029

Study Registration Dates

First Submitted

October 8, 2025

First Submitted That Met QC Criteria

October 18, 2025

First Posted (Actual)

October 21, 2025

Study Record Updates

Last Update Posted (Actual)

February 4, 2026

Last Update Submitted That Met QC Criteria

January 31, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RYXWWMJUDPM6-Bachelorettes

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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