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Active, not recruiting Not applicable

Music and Puzzle Use in Dysmenorrhea Relief

NCT07081789 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-01
Last updated
2025-07-23

Condition(s) studied

Dysmenorrhea

Investigational drug(s) / intervention(s)

Music ListeningPuzzle Activity

Music Listening: Participants will listen to a 24 min 54 sec music track for 4 days (starting 3 days before menstruation).

Puzzle Activity: Participants will do puzzles for the same duration and timing.

Study summary

The aim of this clinical trial is to evaluate whether interventions such as listening to music and doing puzzles are effective in reducing menstrual pain, menstrual symptoms, and perceived stress in young women with dysmenorrhea, ages 18-25.

The main questions it aims to answer are:

Do listening to music and doing puzzles reduce dysmenorrhea pain? Do these interventions affect menstrual symptoms and perceived stress? The researchers will compare music, puzzle, and control groups to assess the effects on pain intensity, menstrual symptoms, and perceived stress levels.

Participants:

Participants will be followed for three menstrual cycles, In the first cycle, pain, symptoms, and stress levels will be measured,

In the next two cycles:

Music group: Listen to a specific song with headphones for four days, Puzzle group: Do puzzles for the same amount of time, Control group: Measurements only, without intervention.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria * Female students studying at a university health college * Female students between the ages of 18 and 25 * Female students with a Visual Analog Scale (100 mmVAS) pain intensity of 5 or higher * Female students with regular menstrual cycles (28 ± 7 days) within the past year * Female students without endocrine, neurological, or chronic diseases such as pelvic pathology, hearing loss, diabetes, and heart disease * Female students without psychiatric illnesses or mental health problems that would interfere with evaluation and cooperation * Female students who are not using oral contraceptives or antidepressants * Female students who have not had pelvic surgery * Female students who have not had malignant diseases * Female students who are not obese * Female students who have not previously been pregnant * Female students who have not received advanced musical training * Female students who are not taking vitamin supplements Exclusion Criteria * Female students who do not meet the inclusion criteria * Female students who use medication, non-drug practices (acupressure, Reiki, reflexology, meditation), or any nutritional supplements to reduce pain

Primary outcome measure(s)

  • Menstrual Pain Severity — Through study completion, an average of 3 mounts
    Menstrual pain intensity will be assessed using the 100 mm Visual Analog Scale (VAS). Participants will rate their pain by marking a point on a 10 cm horizontal line ranging from 0 ("no pain") to 10 ("worst imaginable pain"). Higher scores indicate more severe pain.

Trial sites (1)

FacilityCityRegionStatus
Bucak Health School Burdur Bucak
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07081789 on ClinicalTrials.gov ↗ ← All trials in Turkey