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The effect of guided visualization on fibroid symptoms

Not Applicable
Recruiting
Conditions
terine fibroid.
Leiomyoma of uterus
Registration Number
IRCT20160608028352N10
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
72
Inclusion Criteria

Willingness to participate in the study
Age 24 to 45 years
Having at least third grade of junior high school education
Uterine fibroid diagnosis confirmed by ultrasound
Having complications of fibroids, such as heavy menstrual bleeding and fibroid pain (that have been confirmed by a gynecologist and have not received medical treatment before).
Not having any underlying diseases or major psychiatric disorders.

Exclusion Criteria

Menopause
Lack of cooperation in treatment
Unwillingness to continue participating in the study
The need for surgical interventions during the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before the intervention, immediately after the intervention and two months after the last counseling. Method of measurement: McGill pain questionnaire.;Need to Pain reliever. Timepoint: Before the intervention, immediately after the intervention and three months after the last counseling. Method of measurement: self reporting.
Secondary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: Before the intervention, immediately after the intervention and two months after the last counseling. Method of measurement: Higham chart.
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