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Not Yet RecruitingNCT06383312

Magnetic Reflexologic Insoles for Primary Dysmenorrhea

Investigation of the Effectiveness of Reflexologic Magnetic Insoles on Dysmenorrhea Symptoms in Primary Dysmenorrhea

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Istanbul Medipol University Hospital · Academic / Other
Sex
Female
Age
18 Years – 30 Years
Healthy volunteers
Not accepted

Summary

In the study, easy-to-access and easy-to-use reflexologic magnetic insoles were used in women with primary dysmenorrhea who did not want to receive medical treatment; In addition to reducing symptoms such as pain, nausea, dizziness, fainting, vomiting, weakness, constipation/acute gastroenteritis, it is aimed to increase individuals' participation in daily life activities and increase their quality of life by increasing their emotional state.

Detailed description

60 women diagnosed with primary dysmenorrhea through examination by a gynecologist will be included in the study. 60 women will be randomly divided into 2 groups. These groups; Reflexologic Magnetic Insoles Sham Group: They will use orthopedic insoles.

Conditions

Interventions

TypeNameDescription
DEVICEReflexologic Magnetic Insole GroupReflexologic magnetic insole will be used for at least 7 hours a day, every day, for 12 weeks in participants diagnosed with primary dysmenorrhea. Then the effectiveness of the insoles will be compared.
DEVICEOrthopedic Insole GroupOrthopedic insole (sham) will be used for at least 7 hours a day, every day, for 12 weeks in participants diagnosed with primary dysmenorrhea. Then the effectiveness of the insoles will be compared.

Timeline

Start date
2024-05-01
Primary completion
2024-08-01
Completion
2024-09-01
First posted
2024-04-25
Last updated
2024-04-25

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06383312. Inclusion in this directory is not an endorsement.