The Effect of Distraction Techniques Used in Intramuscular (IM) Injections on Pain in Adolescents Presenting to the Emergency Department With Dysmenorrhea: A Randomized Controlled Study
Recruiting now · Not applicable
Conditions studied: Dysmenorrhea, Pain, Distraction Methods
In brief
Brief Summary: This study investigates the effectiveness of non-pharmacological techniques for managing dysmenorrhea (menstrual pain) in adolescents. The study focuses on methods such as Helfer Skin Tap Technique (HSTT) and ShotBlocker, which aim to reduce pain without medication. The goal is to determine how these techniques can help adolescents manage their pain more effectively. The study targets adolescents aged 12-18 who experience menstrual pain. Participants will be monitored over several months to assess the impact of these techniques on their pain levels, emotional well-being, and daily activities. Participation in the study poses minimal risks. However, the effectiveness of these pain management techniques may vary from person to person. By the end of the study, the aim is to improve pain management strategies for adolescents and gain a better understanding of the effectiveness of non-pharmacological treatments for dysmenorrhea.
Key facts
- Study ID
- NCT06842329
- Run by
- Duygu MEZDE
- People needed
- 90
- Starts
- 2024-10-01
- Expected to finish
- 2025-04-01
- Last updated by the study team
- 2025-02-24
Who can join
Age: 12 and older, up to 18. Sex: female. Healthy volunteers: not accepted.
You may not qualify if…
- Individuals with severe cardiovascular, neurological, or other serious medical conditions.
- Pregnant individuals.
- Individuals undergoing regular hormonal therapy or using birth control methods.
- Individuals with significant psychological or physiological conditions related to pain sensitivity (e.g., hyperalgesia).
- Individuals receiving other pharmacological treatments or pain management medications during the study.
Where it is running
- Ladik Devlet Hastanesi — Samsun, Turkey (Türkiye) (enrolling)
Full record on ClinicalTrials.gov
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