Procedure-Related PainKuco-MagicNCT07746973
Magic Show Featuring "Kuco" for Pain and Fear During Invasive Procedures
A study testing Kuco Magic Show in people with Procedure-Related Pain and Procedure-Related Fear, run by Inonu University at 1 site in Turkey (Türkiye).
Trial summary
Children frequently experience pain and fear during invasive procedures such as venipuncture and peripheral intravenous catheter insertion. These experiences may negatively affect children's cooperation during procedures and increase anxiety related to future healthcare encounters. Read more about this study
- Who is it for?
- Ages 5 to 8 yearsHealthy volunteers can take part
- Conditions the study is for
- Procedure-Related Pain, Procedure-Related Fear, Peripheral Intravenous Catheterization
- What is being tested?
- Kuco Magic Show
- Type of treatment
- Injection or infusion, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 29 Jun 2026to 31 Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 5 to 8 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- Children aged 5 to 8 years.
- Requiring venipuncture or peripheral intravenous catheter insertion in the pediatric emergency department, pediatric blood collection unit, or pediatric day-care unit.
- Able to communicate in Turkish.
- Conscious and able to respond to the study scales.
- No visual or hearing impairment that would interfere with participation in the intervention or outcome assessment.
- Parent or legal guardian provides written informed consent, and the child provides assent when appropriate.
Who cannot join
- Presence of a chronic psychiatric or neurological disorder.
- Presence of a severe chronic medical condition that may affect pain or fear perception.
- Administration of analgesic, sedative, or anxiolytic medication before the procedure.
- Previous participation in this study.
- Child or parent refuses to participate or withdraws consent at any stage of the study.
- Failure to complete the invasive procedure or the study assessments.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Official title: The Effect of a Magic Show Featuring "Kuco" on Pain and Fear Experienced During an Invasive Procedure
Children frequently experience pain and fear during invasive procedures such as venipuncture and peripheral intravenous catheter insertion. These experiences may negatively affect children's cooperation during procedures and increase anxiety related to future healthcare encounters. Non-pharmacological distraction techniques are recommended to reduce procedure-related pain and fear in pediatric patients.
This randomized controlled trial aims to evaluate the effect of a standardized magic show featuring "Kuco" on pain and fear experienced by children during invasive procedures. Eighty children aged 5-8 years who require venipuncture or peripheral intravenous catheter insertion will be randomly assigned to either an intervention group or a control group. Children in the intervention group will receive a standardized magic show performed with the "Kuco" puppet before and throughout the invasive procedure, whereas children in the control group will receive routine clinical care only.
Pain and fear will be assessed immediately before and after the procedure using the Wong-Baker FACES Pain Rating Scale and the Children's Fear Scale. The findings are expected to provide evidence regarding the effectiveness of a magic show-based distraction intervention for reducing procedure-related pain and fear in children.
- Conditions
- Procedure-Related Pain, Procedure-Related Fear, Peripheral Intravenous Catheterization, Venipuncture
- Being tested
- Kuco Magic Show
- Keywords
- Pediatric, Children, Magic Show, Distraction, Nonpharmacological Intervention, Pain, Fear, Venipuncture, Peripheral Intravenous Catheterization, Wong-Baker FACES Pain Rating Scale, Children's Fear Scale, Puppet, Kuco
- Medical subject headings
- Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Kuco Magic ShowBehavioural
Also called Kuco Distraction Intervention
Participants assigned to the intervention group will receive a standardized magic show featuring the "Kuco" puppet as a behavioral distraction technique before and throughout the invasive procedure (venipuncture or peripheral intravenous catheter insertion). The intervention will be delivered by a trained researcher using a standardized protocol that includes interactive magic tricks and verbal engagement to maintain the child's attention during the procedure. The magic show will begin approximately 2 minutes before the procedure and continue until the procedure is completed, in addition to routine clinical care.
| Study group | Role | What they receive |
|---|---|---|
| Magic Show Intervention | Experimental | Participants in this arm will receive a standardized magic show featuring the "Kuco" puppet before and throughout the invasive procedure (venipuncture or peripheral intravenous catheter insertion), in addition to routine clinical care. The intervention is designed as a non-pharmacological distraction technique to reduce procedure-related pain and fear. Receives: Behavioral: Kuco Magic Show |
| Control | No intervention | Participants in this arm will receive routine clinical care during venipuncture or peripheral intravenous catheter insertion without any additional distraction intervention. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Procedure-Related Pain
Pain intensity will be assessed using the Wong-Baker FACES Pain Rating Scale immediately before and within 1 minute after the invasive procedure. The scale ranges from 0 to 10, with higher scores indicating greater pain intensity.
Measured: Immediately before and within 1 minute after the invasive procedure.
Procedure-Related Fear
Fear will be assessed using the Children's Fear Scale immediately before and within 1 minute after the invasive procedure. The scale ranges from 0 to 4, with higher scores indicating greater fear.
Measured: Immediately before and within 1 minute after the invasive procedure.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Aug 2026
- Study start29 Jun 2026
- Primary completion31 Dec 2026 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (13)Papers the sponsor has linked to this study.
- Other trials for Procedure-Related PainStudies of the same condition, open and under way.
- More trials run by Inonu UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Inonu University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Abdullah Sarman, Bingol University
- Investigators
- Abdullah Sarman, Associate Professor, Principal investigator, Bingöl University, Faculty of Health Sciences, Department of Pediatric Nursing
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07746973
- Sponsor's protocol ID
- E-60543243-044-2600032415
- Acronym
- Kuco-Magic
- Status last verified
- Jul 2026
- First submitted
- 27 Jul 2026
- Last updated
- 5 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared due to participant confidentiality and data protection considerations. Only aggregated study results will be disseminated.
Publications
Zimmerman, F. J., & Bell, J. F. (2010). Associations of television content type and amount with obesity: A longitudinal study. International Journal of Behavioral Nutrition and Physical Activity, 7(1), 54. https://doi.org/10.1186/1479-5868-7-54
Yılmaz, R., Erkorkmaz, Ü., & Yıldız, H. (2011). Çocuklarda yeme davranışı anketinin Türkçe geçerlik ve güvenirlik çalışması. Anadolu Psikiyatri Dergisi, 12(4), 287-294.
Wardle J, Guthrie CA, Sanderson S, Rapoport L. Development of the Children's Eating Behaviour Questionnaire. J Child Psychol Psychiatry. 2001 Oct;42(7):963-70. doi: 10.1111/1469-7610.00792.
PubMed 11693591Rideout, V., & Robb, M. B. (2020). The Common Sense census: Media use by kids age zero to eight. Common Sense Media. https://www.commonsensemedia.org/sites/default/files/research/report/2020_zero_to_eight_census_final_web.pdf
Öztürk, M., & Akçay, D. (2024). Okul öncesi dönem çocuklarında ekran maruziyeti ve beslenme alışkanlıkları üzerine bir inceleme. Sağlık Bilimleri ve Meslekleri Dergisi, 11(1), 45-58.
McArthur, B. A., Browne, D., McDonald, S., Tough, S., & Madigan, S. (2022). Longitudinal associations between screen time and children's developmental milestones. JAMA Pediatrics, 176(1), 52-60. https://doi.org/10.1001/jamapediatrics.2021.4686
Harris JL, Bargh JA, Brownell KD. Priming effects of television food advertising on eating behavior. Health Psychol. 2009 Jul;28(4):404-13. doi: 10.1037/a0014399.
PubMed 19594263Furuncu, M., & Öztürk, E. (2020). Okul öncesi çocuklarda problemli medya kullanımının değerlendirilmesi: Geçerlik ve güvenirlik çalışması. Çocuk ve Gençlik Ruh Sağlığı Dergisi, 27(3), 173-183.
Furuncu, M. (2020). Okul öncesi dönem çocuklarda problemli medya kullanımının ebeveyn tutumları ve çocuk özellikleri açısından incelenmesi. Yayımlanmamış yüksek lisans tezi, İstanbul Üniversitesi-Cerrahpaşa.
Domoff, S. E., Radesky, J. S., Harrison, K., Riley, H., Lumeng, J. C., Miller, A. L., & Gearhardt, A. N. (2020). A prospective study of television in the home, television in the bedroom, and overweight/obesity from infancy to middle childhood. Pediatric Obesity, 15(4), e12601. https://doi.org/10.1111/ijpo.12601
Domoff SE, Harrison K, Gearhardt AN, Gentile DA, Lumeng JC, Miller AL. Development and Validation of the Problematic Media Use Measure: A Parent Report Measure of Screen Media "Addiction" in Children. Psychol Pop Media Cult. 2019 Jan;8(1):2-11. doi: 10.1037/ppm0000163. Epub 2017 Nov 16.
PubMed 30873299Boyland EJ, Whalen R. Food advertising to children and its effects on diet: review of recent prevalence and impact data. Pediatr Diabetes. 2015 Aug;16(5):331-7. doi: 10.1111/pedi.12278. Epub 2015 Apr 21.
PubMed 25899654Aman, M. G., Arnold, L. E., & Hollway, J. A. (2022). Digital media and eating behaviors in early childhood: A systematic review. Appetite, 168, 105884. https://doi.org/10.1016/j.appet.2021.105884
Study at a glance
From the registry record, last updated by the sponsor on 5 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of a Magic Show Featuring "Kuco" on Pain and Fear Experienced During an Invasive Procedure
- ClinicalTrials.gov ID
- NCT07746973
- Acronym / sponsor ID
- Kuco-Magic / E-60543243-044-2600032415
- Conditions
- Procedure-Related Pain, Procedure-Related Fear, Peripheral Intravenous Catheterization, Venipuncture
- Keywords
- Pediatric, Children, Magic Show, Distraction, Nonpharmacological Intervention, Pain, Fear, Venipuncture
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Inonu UniversityUniversity, hospital or other
- Study start
- 29 Jun 2026 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 5 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Children frequently experience pain and fear during invasive procedures such as venipuncture and peripheral intravenous catheter insertion. These experiences may negatively affect children's cooperation during procedures and increase anxiety related to future healthcare encounters. Non-pharmacological distraction techniques are recommended to reduce procedure-related pain and fear in pediatric patients.
This randomized controlled trial aims to evaluate the effect of a standardized magic show featuring "Kuco" on pain and fear experienced by children during invasive procedures. Eighty children aged 5-8 years who require venipuncture or peripheral intravenous catheter insertion will be randomly assigned to either an intervention group or a control group. Children in the intervention group will receive a standardized magic show performed with the "Kuco" puppet before and throughout the invasive procedure, whereas children in the control group will receive routine clinical care only.
Pain and fear will be assessed immediately before and after the procedure using the Wong-Baker FACES Pain Rating Scale and the Children's Fear Scale. The findings are expected to provide evidence regarding the effectiveness of a magic show-based distraction intervention for reducing procedure-related pain and fear in children.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Magic Show Intervention | Experimental | Behavioral: Kuco Magic ShowParticipants in this arm will receive a standardized magic show featuring the "Kuco" puppet before and throughout the invasive procedure (venipuncture or peripheral intravenous catheter insertion), in addition to routine clinical care. The intervention is designed as a non-pharmacological distraction technique to reduce procedure-related pain and fear. |
| Control | No intervention | –Participants in this arm will receive routine clinical care during venipuncture or peripheral intravenous catheter insertion without any additional distraction intervention. |
Who may qualify
- Ages
- 5 to 8 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (6 listed)
- Children aged 5 to 8 years.
- Requiring venipuncture or peripheral intravenous catheter insertion in the pediatric emergency department, pediatric blood collection unit, or pediatric day-care unit.
- Able to communicate in Turkish.
- Conscious and able to respond to the study scales.
- No visual or hearing impairment that would interfere with participation in the intervention or outcome assessment.
Key exclusion criteria (6 listed)
- Presence of a chronic psychiatric or neurological disorder.
- Presence of a severe chronic medical condition that may affect pain or fear perception.
- Administration of analgesic, sedative, or anxiolytic medication before the procedure.
- Previous participation in this study.
- Child or parent refuses to participate or withdraws consent at any stage of the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Kuco Magic ShowAlso: Kuco Distraction InterventionParticipants assigned to the intervention group will receive a standardized magic show featuring the "Kuco" puppet as a behavioral distraction technique before and throughout the invasive procedure (venipuncture or peripheral intravenous catheter insertion). The intervention will be delivered by a trained researcher using a standardized protocol that includes interactive magic tricks and verbal engagement to maintain the child's attention during the procedure. The magic show will begin approximately 2 minutes before the procedure and continue until the procedure is completed, in addition to routine clinical care. | Behavioural | Magic Show Intervention |
Primary outcome
Procedure-Related Pain
Time frame: Immediately before and within 1 minute after the invasive procedure.
Pain intensity will be assessed using the Wong-Baker FACES Pain Rating Scale immediately before and within 1 minute after the invasive procedure. The scale ranges from 0 to 10, with higher scores indicating greater pain intensity.
Procedure-Related Fear
Time frame: Immediately before and within 1 minute after the invasive procedure.
Fear will be assessed using the Children's Fear Scale immediately before and within 1 minute after the invasive procedure. The scale ranges from 0 to 4, with higher scores indicating greater fear.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Aug 2026.
- BackgroundZimmerman, F. J., & Bell, J. F. (2010). Associations of television content type and amount with obesity: A longitudinal study. International Journal of Behavioral Nutrition and Physical Activity, 7(1), 54. https://doi.org/10.1186/1479-5868-7-54
- BackgroundYılmaz, R., Erkorkmaz, Ü., & Yıldız, H. (2011). Çocuklarda yeme davranışı anketinin Türkçe geçerlik ve güvenirlik çalışması. Anadolu Psikiyatri Dergisi, 12(4), 287-294.
- Background: PubMed 11693591Wardle J, Guthrie CA, Sanderson S, Rapoport L. Development of the Children's Eating Behaviour Questionnaire. J Child Psychol Psychiatry. 2001 Oct;42(7):963-70. doi: 10.1111/1469-7610.00792.
- BackgroundRideout, V., & Robb, M. B. (2020). The Common Sense census: Media use by kids age zero to eight. Common Sense Media. https://www.commonsensemedia.org/sites/default/files/research/report/2020_zero_to_eight_census_final_web.pdf
- BackgroundÖztürk, M., & Akçay, D. (2024). Okul öncesi dönem çocuklarında ekran maruziyeti ve beslenme alışkanlıkları üzerine bir inceleme. Sağlık Bilimleri ve Meslekleri Dergisi, 11(1), 45-58.
- BackgroundMcArthur, B. A., Browne, D., McDonald, S., Tough, S., & Madigan, S. (2022). Longitudinal associations between screen time and children's developmental milestones. JAMA Pediatrics, 176(1), 52-60. https://doi.org/10.1001/jamapediatrics.2021.4686
- Background: PubMed 19594263Harris JL, Bargh JA, Brownell KD. Priming effects of television food advertising on eating behavior. Health Psychol. 2009 Jul;28(4):404-13. doi: 10.1037/a0014399.
- BackgroundFuruncu, M., & Öztürk, E. (2020). Okul öncesi çocuklarda problemli medya kullanımının değerlendirilmesi: Geçerlik ve güvenirlik çalışması. Çocuk ve Gençlik Ruh Sağlığı Dergisi, 27(3), 173-183.
- BackgroundFuruncu, M. (2020). Okul öncesi dönem çocuklarda problemli medya kullanımının ebeveyn tutumları ve çocuk özellikleri açısından incelenmesi. Yayımlanmamış yüksek lisans tezi, İstanbul Üniversitesi-Cerrahpaşa.
- BackgroundDomoff, S. E., Radesky, J. S., Harrison, K., Riley, H., Lumeng, J. C., Miller, A. L., & Gearhardt, A. N. (2020). A prospective study of television in the home, television in the bedroom, and overweight/obesity from infancy to middle childhood. Pediatric Obesity, 15(4), e12601. https://doi.org/10.1111/ijpo.12601
- Background: PubMed 30873299Domoff SE, Harrison K, Gearhardt AN, Gentile DA, Lumeng JC, Miller AL. Development and Validation of the Problematic Media Use Measure: A Parent Report Measure of Screen Media "Addiction" in Children. Psychol Pop Media Cult. 2019 Jan;8(1):2-11. doi: 10.1037/ppm0000163. Epub 2017 Nov 16.
- Background: PubMed 25899654Boyland EJ, Whalen R. Food advertising to children and its effects on diet: review of recent prevalence and impact data. Pediatr Diabetes. 2015 Aug;16(5):331-7. doi: 10.1111/pedi.12278. Epub 2015 Apr 21.
- Individual participant dataSharing planned: No. Individual participant data will not be shared due to participant confidentiality and data protection considerations. Only aggregated study results will be disseminated.
Related trials for Procedure-Related Pain
Recruiting
Opioid and Pain Treatment in Indigenous Communities (OPTIC) Trial
Opioid Use Disorder, Opioid Misuse
Not yet recruiting
Music Listening for Chronic Pain in Adults With Early-Stage Dementia
Chronic Pain, Alzheimer Disease
Active, not recruiting
Pain Self-Management and Treatment Engagement for Patients Taking Opioids
Chronic Pain, Opioid Use Disorder
Recruiting
Impact of Virtual Reality on Anxiety in Patients Undergoing Interventional Procedures
Anxiety
Recruiting
Mindfulness in Fracture Recovery and Reduction of Opioid Reliance: Evaluating the Feasibility of Implementing a Brief, Mindfulness-based Intervention to Manage Pain and Anxiety Before and After Fracture Surgery
Orthopaedic Fractures, Orthopaedic Trauma Fractures and Non-unions
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Abdullah Sarman, Associate Professor principal investigator
Bingöl University, Faculty of Health Sciences, Department of Pediatric Nursing
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Kuco Magic Show in people with Procedure-Related Pain and Procedure-Related Fear, run by Inonu University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 5 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Procedure-Related Pain (time frame: Immediately before and within 1 minute after the invasive procedure.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07746973, which also lists 13 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Aug 2026.