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Holistic Medicine Treatment of Uterine Fibroids-Adults

NCT07219381 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2026-02-04

No results posted yet for this study

Summary

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.

Conditions

  • Uterine Fibroids - 1St Diagnosis
  • Uterine Fibroids Affecting Pregnancy
  • Uterine Fibroid Degenerated

Interventions

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).

Sponsors & Collaborators

  • Virtual Tribunal Monastery

    lead OTHER

Principal Investigators

  • Jones · Humanitarian Veterans Association

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-26
Primary Completion
2029-01-19
Completion
2029-01-19

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07219381 on ClinicalTrials.gov