Status:

COMPLETED

The Effect of Acupressure on Pain, Menstrual Symptoms, and General Comfort in Adolescents with Primary Dysmenorrhea

Lead Sponsor:

Mersin University

Conditions:

Pain

Dysmenorrhea Primary

Eligibility:

FEMALE

14-17 years

Phase:

NA

Brief Summary

In this study, it is planned to determine the effect of acupressure applied to adolescents with primary dysmenorrhea on pain, menstrual symptoms and general comfort. The research questions of the rese...

Detailed Description

Methods: Adolescents aged 14-17 years with primary dysmenorrhea will be randomly assigned to the acupressure and control groups. The study group (n=26) and placebo group (n=26) will be applied to the...

Eligibility Criteria

Inclusion

  • Those between the ages of 14-17,
  • Willing to participate in the research,
  • Open to communication,
  • Having a regular menstrual period (occurring at intervals of 21-35 days and lasting 3-8 days),
  • Menstrual pain severity is at least 4 according to the Visual Pain Scale,
  • A score of 60 or more on the Menstruation Symptom Scale,
  • Not using hormonal contraception and intrauterine device,
  • Not pregnant and not experiencing pregnancy before,
  • Does not have a systemic and chronic disease,
  • Have not had a gynecological disorder or surgery before,
  • Not using analgesics 6 hours before and during the study period,
  • Body mass index \<30 kg/m2
  • No physical/mental health problems that would prevent/limit acupressure and exercise,
  • Not doing regular acupressure,
  • No psychiatric problems
  • Adolescents without active COVID-19 infection.

Exclusion

  • Not between the ages of 14-17,
  • Not willing to participate in the research,
  • Closed to communication,
  • Not having a regular menstrual period (not occurring at intervals of 21-35 days and lasting more or less than 3-8 days),
  • Menstrual pain severity is less than 4 according to the Visual Pain Scale,
  • A score below 60 on the Menstruation Symptom Scale,
  • Using hormonal contraception and intrauterine device,
  • Pregnant and experienced pregnancy before,
  • Having a systemic and chronic disease,
  • Have had a previous gynecological disorder or surgery,
  • Using analgesics 6 hours before and during the study period,
  • Body mass index ≥30 kg/m2
  • Having physical/mental health problems that will prevent/limit acupressure and exercise,
  • Regular acupressure
  • Having a psychiatric problem
  • Adolescents with active COVID-19 infection.

Key Trial Info

Start Date :

April 17 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 15 2023

Estimated Enrollment :

56 Patients enrolled

Trial Details

Trial ID

NCT05408611

Start Date

April 17 2023

End Date

November 15 2023

Last Update

January 9 2025

Active Locations (1)

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Mersin University

Yenişehir, Mersin, Turkey (Türkiye), 33140