Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06741059

Effect of TENS on Pain and Symptoms in Primary Dysmenorrhea

Led by Osmaniye Korkut Ata University · Updated on 2025-03-20

93

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The Effect of Transcutaneous Electrical Nerve Stimulation (TENS) on Pain and Menstrual Symptoms in Primary Dysmenorrhea This study aims to investigate the effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) in managing pain and alleviating menstrual symptoms in individuals with primary dysmenorrhea. Primary dysmenorrhea is characterized by severe menstrual pain and accompanying symptoms that negatively impact the quality of life and daily functioning. TENS, a non-invasive and drug-free method, is applied to relieve pain by stimulating nerves through electrical impulses. This research evaluates the impact of TENS on both the intensity of menstrual pain and associated symptoms, offering insights into its potential as an alternative or complementary therapeutic approach.

CONDITIONS

Official Title

Effect of TENS on Pain and Symptoms in Primary Dysmenorrhea

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 and above
  • Have regular menstrual cycles lasting 3 to 8 days, with a cycle length of 21 to 35 days
  • Experience dysmenorrhea pain severity rated 4 or higher on the Visual Analog Scale (VAS)
Not Eligible

You will not qualify if you...

  • Have secondary dysmenorrhea
  • Use oral contraceptives
  • Have impaired tissue integrity in the abdominal area
  • Have previous experience with TENS
  • Have a history of nerve damage or sensory loss
  • Have a pacemaker
  • Have any systemic diseases
  • Are pregnant or in the postpartum period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Esra Ünal

Osmaniye, Turkey (Türkiye), 80010

Actively Recruiting

Loading map...

Research Team

E

Esra U Unal, Doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here