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Clinical Trials/NCT04910529
NCT04910529
Completed
Not Applicable

The Effect of Yoga Practice on Pain Intensity, Menstruation Symptoms and Quality of Life in Nursing Students With Primary Dysmenorrhea

Mersin University1 site in 1 country60 target enrollmentStarted: May 20, 2021Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Pain will evaluate using The The Short Form of the McGill Pain Questionnaire

Overview

Brief Summary

The aim of this randomized controlled study is to evaluate the effect of yoga practice on pain intensity, menstruation symptoms and quality of life in nursing students with primary dysmenorrhea. The hypothesis of this study is that yoga reduces pain and menstrual symptom severity and improves quality of life.

Detailed Description

In the study, 52 students will be randomly assigned to intervention (yoga) and control groups. The researcher will provide information about the purpose of the study and the study process by interviewing all the students in the sample online. All students participating in the study, who are in the yoga or control group of the study, will be given a data collection form as a pre-test by the researcher.

Hatha yoga will be applied to the students (n = 26) in the yoga group in the study. Considering the studies conducted with these students, it is planned to practice Hatha yoga for 60 minutes twice a week for three menstrual cycles (12 weeks). Yoga practice will be done online by the researcher Aslıhan Aksu (A.A.), who has a Yoga Alliance-approved yoga instructor certificate, on the determined days and times using appropriate platforms. In the control group (n=26), no intervention will be made for 12 weeks. The results will be collected through data collection forms before the yoga practice and after the 12-week yoga practice is completed. The data collection forms applied to all students in the yoga and control groups at the beginning of the study will be applied to the control group again at the end of 12 weeks. The primary expected result of the study is the effect of yoga on students' menstrual pain intensity. The secondary expected results of the study are to determine the effect of yoga on students' menstrual symptoms and quality of life.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Masking Description

Participants and the researcher who carried out the application Aslıhan Aksu (A.A.) cannot be blinded due to the nature of the study. When the study is completed, the control and experimental groups will be coded as A and B and the data will be transferred to the computer environment by an independent researcher. The data coded as A and B will be analyzed by a statistician and the findings will be reported.

Eligibility Criteria

Ages
18 Years to 24 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Accepting voluntarily to participate in the study.
  • Studying in 1st and 2nd grade between 18 October 2021-16 September 2022 at Mersin University Faculty of Nursing in the Academic Year of 2021-2022,
  • Between the ages of 18-24 years,
  • Willing to participate in the study,
  • Having the facilities (computer, internet, etc.) to participate in the online training,
  • Having female gender and a regular menstruation period (occurring at intervals of 21-35 days and lasting 3-8 days),
  • Having menstrual pain intensity at least 4 points according to the Visual Pain Scale,
  • Having a score of 60 or more according to the Menstruation Symptom Scale,
  • Not using hormonal contraception and intrauterine equipment,
  • Not pregnant and have not experienced pregnancy before,

Exclusion Criteria

  • Not accepting voluntarily to participate in the study.
  • Studying in Mersin University Nursing Faculty in the 1st and 2nd grade except 18 October 2021-16 September 2022 in the Academic Year of 2021-2022,
  • Younger than 18 years old or over 24 years old,
  • Not having the facilities (computer, internet, etc.) to participate in the online training,
  • Not having female gender and a regular menstruation period,
  • Menstrual pain intensity less than 4 points according to the Visual Pain Scale,
  • Having a score of 59 or less according to the Menstruation Symptom Scale,
  • Using hormonal contraception and intrauterine device,
  • Pregnant and have experienced pregnancy before,
  • Having a systemic and chronic disease,

Outcomes

Primary Outcomes

Pain will evaluate using The The Short Form of the McGill Pain Questionnaire

Time Frame: Change from before implementation and 12th week of practice

The main component of the The Short Form of the McGill Pain Questionnaire (SF-MPQ) consists of 15 descriptors (11 sensory; 4 affective) which are rated on an intensity scale as 0=none, 1=mild, 2=moderate or 3=severe. In this section, sensory (0-33 points), affective (0-12 points) and total (0-45 points) pain quality scores are obtained. The increase in the total pain scores indicates an increase in the perception of pain. The SF-MPQ also includes the Present Pain Intensity (PPI) Index of the Standard MPQ and a Visual Analogue Scale (VAS).

Secondary Outcomes

  • Menstrual symptoms will evaluate using the Menstrual Symptom Questionnaire(Change from before implementation and 12th week of practice.)
  • Quality of life will evaluate using SF-36 Quality of Life Questionnaire(Change from before implementation and 12th week of practice)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aslıhan Aksu

Research Assistant

Mersin University

Study Sites (1)

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