Using distraction techniques to reduce pain during injections in adolescents with menstrual pain
Official title: "The Effectiveness of Helfer Skin Tap Technique and ShotBlocker in Reducing Pain Severity During Intramuscular Injections in Adolescent Dysmenorrhea: A Randomized Controlled Trial"
Run by Ondokuz Mayıs University · NCT06842329 · Data updated 2026-11-12
This study tests if distraction techniques like the Helfer Skin Tap Technique and ShotBlocker can help reduce pain during injections for teenagers who have menstrual pain.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 18 Years |
| Sex | Women only |
| Enrollment | 90 (estimated) |
| Sponsor | Ondokuz Mayıs University Academic / other |
| Locations | 1 site (Samsun) |
| Status | Recruiting |
| Started | October 1, 2024 |
| Main results expected | April 1, 2025 |
| Study ends | April 1, 2025 |
| Registry record updated | February 24, 2025 |
| Trial ID | NCT06842329 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adolescent girls aged 12-18 who experience dysmenorrhea and present to the emergency department.
✕Probably not a fit
Patients with severe medical conditions, pregnant individuals, or those undergoing hormonal therapy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of non-pharmacological techniques, specifically the Helfer Skin Tap Technique (HSTT) and ShotBlocker, in managing dysmenorrhea pain during intramuscular injections in adolescents. It is a randomized controlled trial comparing these techniques against standard injection procedures. Participants aged 12-18 who present with menstrual pain will be monitored to assess the impact on pain levels and overall well-being. The goal is to improve pain management strategies for adolescents experiencing dysmenorrhea.
Why it matters
Potential benefit: If successful, this study could provide effective non-medication-based pain management options for adolescents suffering from menstrual pain.
How similar studies have gone: Other studies have shown promise in using non-pharmacological techniques for pain management, but this specific approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
nclusion Criteria: * Adolescents aged 12-18 years. * Experience of dysmenorrhea (menstrual pain) during at least one menstrual cycle. * Adolescents presenting to the emergency department with dysmenorrhea. * Written informed consent from participants or their legal guardians. Exclusion Criteria: * 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's running
-
Ladik Devlet Hastanesi
Samsun, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Duygu Mezde, MSN
- Email: duygu.mezde@hotmail.com
- Phone: +905418848596
Similar studies
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A randomized trial tests whether Diaphragm-Pelvic Floor Synergy training can reduce menstrual pain and improve quality of life in university-aged women with primary dysmenorrhea.
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Aerobic Exercise vs. Jacobson’s Relaxation for Primary Dysmenorrhea
This study tests whether aerobic exercise or Jacobson’s progressive relaxation can help reduce pain and fatigue and improve quality of life for young women with primary dysmenorrhea.
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This will test whether sacral release or lumbar mobilization works better to reduce menstrual pain, lessen symptoms, and improve quality of life in adolescent girls with primary dysmenorrhea.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.