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The Effect of Music on Pain, Anxiety and Satisfaction During Intrauterine Device Application

The Effect of Music on Pain, Anxiety and Satisfaction During Intrauterine Device Application

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06215183
Enrollment
70
Registered
2024-01-22
Start date
2023-06-01
Completion date
2024-02-01
Last updated
2026-07-15

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

Conditions

Pain, Reproductive Health, Women Health

Keywords

Intrauterine device, Pain, Anxiety, Satisfaction

Brief summary

This study was planned to determine the effect of music listened to during intrauterine device application on pain,anxiety and satisfaction.

Detailed description

The randomized controlled and experimental study will be conducted with 70 women who apply to a Maternal and Child Health and Family Planning Center to have an Intrauterine Device (IUD). Women in the experimental group (n=35) will listen to music before, during and after the IUD application process, and the control group (n=35) will undergo routine IUD application. Information Form containing sociodemographic information, Situational Anxiety

Interventions

OTHERMusic therapy

Women applying for IUD application will receive music therapy for 5 minutes before the procedure, during the IUD application, and for 5 minutes after the procedure.

Sponsors

Sümeyye Köse
Lead SponsorOTHER

Study design

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

Masking description

The evaluation was made by the participants in the study.

Intervention model description

The study is a randomized controlled trial.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Knowing how to read and write, * Not having had an IUD inserted before, * Being between the ages of 18-49, * No hearing-related problems, * Not having used analgesic or anesthetic medication within 24 hours before or during the procedure, * Voluntarily participating in the study,

Exclusion criteria

* The woman has a cognitive and auditory problem * Having a history of cervical surgery

Design outcomes

Primary

MeasureTime frameDescription
Anxiety30 minütesData will be collected using the State Anxiety Inventory. The answer options collected in four classes on the State Anxiety Inventory scale are: (1) Not at all, (2) A little, (3) A lot and (4) Completely; The options on the trait anxiety scale are (1) Rarel, (2) Sometimes, (3) A lot of the time, and (4) Almost always. The higher the score obtained from the scales, the higher the person's anxiety is. The total score obtained from the scale varies between 20-80, and 20-39 indicates a mild anxiety level, 40-59 indicates a medium anxiety level, 60-79 indicates a high anxiety level, and 80 points indicates a panic anxiety level.
Pain Level30 minütesData will be collected using the Visual Analogue Scale. Pain can be given a score between 0 and 10 on the scale.The higher the scale score, the greater the pain.

Secondary

MeasureTime frameDescription
Satisfaction Level30 minütesData will be collected using the Visual Analog Scale. Satisfaction can be given a score between 0 and 10 on the scale. The higher the scale score, the higher the satisfaction level.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026