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The Effect of Su Jok on Dysmenorrhea

The Effect of Su Jok on Dysmenorrhea:Randomized Placebo-Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06896851
Enrollment
34
Registered
2025-03-26
Start date
2024-03-01
Completion date
2024-06-30
Last updated
2025-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysmenorrhea

Keywords

dysmenorrhea, pain, su jok

Brief summary

This study aims to determine the effect of Su Jok application in reducing menstrual pain.The main question it aims to answer is -Is Su Jok practice effective in reducing the severity of dysmenorrhea? The researcher will perform a sham application to see the effect of the application. Participants will perform the application on the first day they have pain during their 3 menstrual cycles. They will evaluate and record their pain with VAS.

Interventions

OTHERSu Jok

a type of acupressure includs hand massage

OTHERSham point using

unrelated point using for acupressing

Sponsors

Ankara Medipol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* regular menstrual cycles (21-35 days) * have abdominal pain in the last three cycles * Those who want to participate in the study as a volunteer

Exclusion criteria

* have any health problems that may affect the menstrual cycle (ovarian cysts, etc. * use hormonal medications

Design outcomes

Primary

MeasureTime frameDescription
Pain assesment Every hour until 4 hours after the onset of pain on the first day of the cycle (each cycle is 28-35 days) and it will be for 3 cycle.Pain assessment is made with Visual Analog Scale(0-10 points, high score means pain severity is high) in three menstrual cycles (up to 105 days).

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026