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NCT04320641 Clinical Trial

The Effect of Acupressure and Yoga on Premenstrual Symptoms and Quality of Life

Nursing Caries Clinical Trial

Official title:
The Effect of Acupressure and Yoga on Premenstrual Symptoms and Quality of Life in Coping With PMS

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04320641
Other study ID # Inonu Universty
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2019
Est. completion date January 10, 2020

Study information
Verified date March 2020
Source Adiyaman University Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research was carried out to determine the effect of acupressure and yoga applied to cope with PMS on premenstrual symptoms and quality of life.

Recruitment information / eligibility
Status Completed
Enrollment 153
Est. completion date January 10, 2020
Est. primary completion date July 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 19 Years and older
Eligibility Inclusion Criteria:

- have regular menstrual cycle

Exclusion Criteria:

- Has a psychiatric diagnosis,

- Having any gynecological disease (anornal uterine bleeding, fibroids, ovarian cyst etc.)

- Using contraceptive drugs,

- With tissue deformity in its extremities, Any health problems that may prevent physical exercise

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• ACUPRESSURE
Acupressure points were determined in a certain order considering the direction of the meridian. The order of application was in the form of Spleen 6th point (SP 6) and 4 point of the Large Intestine (Li 4). In total, 4 points in the upper / lower extremities and 6 acupressure points along with parallel points were studied in each attempt.

Locations
Country Name City State
Turkey Didem Simsek Kucukkelepce Adi?yaman

Sponsors (1)
Lead Sponsor Collaborator
Adiyaman University Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary premenstrual syndrome scale 12 weeks
Primary WHOQOL-BREF-TR 12 weeks
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