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NCT06949397

The Effect of the Menstrual Belt Stress Ball on Pain in Women With Dysmenorrhea

Completed NA Last updated 29 April 2025
What this trial tests

NA trial testing Change in VAS voice performance score following the characteristics of the menstrual cycle of two women in Education in 105 participants. Completed in 1 September 2024.

Timeline
30 April 2024
Primary endpoint
1 September 2024
1 September 2024

Quick facts

Lead sponsorIstanbul Gedik University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment105
Start date30 April 2024
Primary completion1 September 2024
Estimated completion1 September 2024
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Istanbul Gedik University

Who can join

Adults 18 to 45, female only, with Education. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will be conducted as a randomized controlled quasi-experimental study to determine the effect of hot massage menstrual belt and stress relief ball application on pain intensity in women with dysmenorrhea. The study will include 105 women with dysmenorrhea (midwife, nurse, doctor, cleaning staff, secretary) who meet the inclusion criteria. Female participants between the ages of 18-45 will be randomly divided into three groups as experimental group 1 (n=35), experimental group 2 (n=35) and control group (n=35) by envelope method. Data will be collected using Informed Consent Form, Descriptive Information Form, Visual Pain Scale (VAS), Dysmenorrhea Impact Scale-Revised Short Form (DIS-R) and Menstrual Symptoms Scale. Descriptive Information Form, Visual Pain Scale (VAS), Dysmenorrhea Impact Scale-Revised Short Form (DIS-R) and Menstrual Symptom Scale will be applied to the three groups before the application. During the application, experimental group 1 will be given a menstrual belt with electric waist heating and vibration for 20 minutes. Experimental group 2 will be given a stress-relieving squeezing ball to feel its soft structure for the same period of time.The third group was determined as the control group and no application will be made. After the application, the participants will be asked to rate their pain intensity using the Visual Pain Scale (VAS) and record their pain scores.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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