Using a vibrating cold device and a marionette doll to reduce pain and fear during blood draws in children
Effect of Bee-buzzy Vibrating Cold Application and Marionette Doll on Pain and Fear During Phlebotomy Among Preschool Children: A Randomized Controlled Study
This study is testing if using a vibrating cold device and a fun marionette doll can help young children feel less pain and fear during blood draws.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 3 Years to 6 Years |
| Sex | All |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Asyut) |
| Trial ID | NCT06443437 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a bee-buzzy vibrating cold application and a marionette doll as non-pharmacological methods to reduce pain and fear in preschool children undergoing phlebotomy. By utilizing distraction techniques, the study aims to minimize the negative experiences associated with blood draws, which can lead to long-term behavioral and physiological issues. The research focuses on children who successfully undergo phlebotomy on the first attempt, ensuring a controlled environment for assessing the interventions' impact on pain perception and anxiety levels.
Who should consider this trial
Good fit: Ideal candidates for this study are preschool children who are undergoing their first successful phlebotomy and whose parents consent to participation.
Not a fit: Patients with chronic diseases, mental disabilities, or those who have recently taken analgesics or had unsuccessful phlebotomy attempts may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce pain and fear in children during medical procedures, improving their overall experience and future healthcare interactions.
How similar studies have performed: Previous studies have shown positive outcomes using similar distraction techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. children and parents who agreed to participate in the study 2. children had successful phlebotomy in the first attempt. Exclusion Criteria: 1. Children who are having a chronic disease 2. Mental disability or mental retardation 3. Taking analgesics in the last 24 hours 4. Undergone a surgical procedure, 5. Not having a successful phlebotomy on the first attempt, 6. The child and his/her family not being willing to participate in the study.
Where this trial is running
Asyut
- Assiut university children hospital — Asyut, Egypt (Recruiting)
Study contacts
- Study coordinator: Shimaa H Khalf allah, post doctor
- Email: shimaa_hassan@aun.edu.eg
- Phone: 01097248758
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.