Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
ID06600230

The Effect of Pelvic Floor-Based Training on Young Women With Dysmenorrhea

Led by Uskudar University · Updated on 2024-09-19

70

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to study the impact of patient education on knowledge and symptoms in young women with primary dysmenorrhea, a common type of menstrual pain without underlying pelvic disease. The study looks at whether education can improve symptoms and how knowledge levels relate to pain. It is a randomized, single-blind trial sponsored by Uskudar University involving women aged 18 to 35 who have regular menstrual cycles and primary dysmenorrhea. Participants are divided into two groups: one receives pelvic floor education and exercise training from physiotherapists over two sessions, while the control group uses conventional self-methods such as rest and heat application when symptoms occur. The education group is asked to perform the exercises taught, and assessments happen before training and after the first menstrual cycle. During the study, participants’ pain levels and pelvic floor knowledge are measured using a visual analog scale and a pelvic floor health knowledge test, respectively. Additionally, the dysmenorrhea affect scale is used to assess symptom impact. Data analysis will examine changes over time and relationships between knowledge and symptoms. The study lasts through one menstrual cycle following education, with careful monitoring of outcomes and symptom changes.

CONDITIONS

Brief Title

Effect of Pelvic Floor-Based Training on Dysmenorrhea

Who Can Participate

Age: 18Years - 35Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Being diagnosed with primary dysmenorrhea
  • Being between the ages of 18-35
  • Having a regular menstrual cycle
  • Volunteering to participate in the study
Not Eligible

You will not qualify if you...

  • Having a history of endometriosis or gynecological pathology
  • Having a history of gynecological disease or surgery
  • Having a neurological or musculoskeletal problem

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 1 menstrual cycle

Participants receive pelvic floor and exercise training or classical self-methods such as rest and heat application to manage dysmenorrhea symptoms.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 1 location

1

Uskudar University

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

T

Tuba Kolaylı, PhD(c)

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Effect of pelvic floor-centered patient education programme in young women with primary dysmenorrhea: A randomized controlled trial.

Tuba Kolaylı Çerezci, Esra Demir, Semanur Eniş...

https://pubmed.ncbi.nlm.nih.gov/41927202