PainNCT05161416
The Effects of Cartoon Watching and Bubble Blowing as Distraction Methods During Venipuncture on Pain, Anxiety, and Fear in Children Aged 6-8 Years
A study testing Bubble Blowing and Cartoon Watching in people with Pain and Anxiety, run by Mersin University at 1 site in Turkey (Türkiye).
Trial summary
Active and passive distraction methods are frequently used in the nursing management of procedural pain in children. There are no studies comparing the effects of cartoon watching (passive) and bubble blowing (active) as distraction methods on pain, anxiety, and fear associated with venipuncture in children. Read more about this study
- Who is it for?
- Ages 6 to 8 years
- What is being tested?
- Bubble Blowing and Cartoon Watching
- Type of treatment
- Pill or oral medicine, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 56 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Oct 2019to 2 Mar 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 6 to 8 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Child aged 6-8 years
- Child with need or plan for venipuncture (antecubital fossa)
Who cannot join
- Child with a neurodegenerative disease, mental retardation, vision and hearing problems, chronic, life-threatening (sepsis, shock, respiratory / cardiac arrest) or genetic disease
- Child with use of opioids, narcotics, analgesics or sedatives in the last 24 hours before the procedure
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Mersin University Hospital
Mersin, Yenişehir, 33343
About this study
Official title: Comparison of the Effects of Cartoon Watching and Bubble Blowing as Distraction Methods During Venipuncture on Pain, Fear, and Anxiety in Children Aged 6-8 Years: A Randomized Experimental Study
Active and passive distraction methods are frequently used in the nursing management of procedural pain in children. There are no studies comparing the effects of cartoon watching (passive) and bubble blowing (active) as distraction methods on pain, anxiety, and fear associated with venipuncture in children.
This study aimed to compare the effects of bubble blowing (active distraction) and cartoon watching (passive distraction) techniques on pain, anxiety, and fear during venipuncture in children aged 6-8 years.
Read the detailed description
Research Hypotheses H1a= There is a difference in the mean WB-FACES score during the procedure between the bubble group (BG) and the cartoon group (CG).
H1b= There is a difference in the mean WB-FACES score after the procedure between the BG and CG groups.
H2a= There is a difference in the mean CSA score during the procedure between the BG and CG groups.
H2b= There is a difference in the mean CSA score after the procedure between the BG and CG groups.
H3a= There is a difference in the mean CFS score during the procedure between the BG and CG groups.
H3b= There is a difference in the mean CFS score after the procedure between the BG and CG groups.
Design and Settings: This parallel-group randomized trial was conducted at the invasive procedure room of the pediatrics department of a university hospital in the East Mediterranean Region of Turkey. For this experimental research, 56 children aged 6-8 years were assigned to two groups (Bubble Group=BG; n = 28 and Cartoon Group=CG; n = 28) using block randomization.
Sample Size: The main trial sample was calculated based on the pilot study findings. The pilot study was conducted with 20 children (BG; n = 10 and CG; n = 10) who met the eligibility criteria. A priori power analysis was performed based on the effect size (d = 0.885, large effect) of the difference in pain scores between the groups (during the procedure) determined in the pilot study. Using G*Power 3.1.9.7, the minimum sample size was calculated as 56 children, with 28 children per group, for a two-tailed hypothesis, an effect size of d = 0.885, an allocation ratio of n1/n2=1, type I error of 0.05, and a power of 90%.
Randomization: Using block randomization, six different combinations of the codes A and B with a block size of 4 (ABAB(1), AABB(2), BABA(3) …) were generated. The combinations were numbered from 1 to 6. The numbers (1-6) were randomly sorted 14 times via randomizer.org and a random allocation sequence was generated. Coin flipping was used to determine which of the codes A and B would be BG and CG (R1). The random allocation sequence, which was placed in opaque envelopes by giving a sequence number, was hidden from the principal researchers (R2, R3) (allocation concealment). The opaque envelopes were stored in a locked cabinet by the researcher who performed the randomization (R1). The group including the eligible children was not shared with R2 and R3 until the intervention.
Data Collection Tools Socio-Demographic Data Collection and Procedure Follow-up Form: It includes "age, gender, previous experience of hospitalization, experience of procedural pain in last week, analgesic administration at least six hours before the procedure, size of peripheral IV needle, area of IV blood sample, parental presence during procedure, and baseline data of pain, anxiety and fear scores of children before procedure".
The Wong-Bakers FACES® Pain Rating Scale (WB-FACES): Developed by Wong and Baker in 1981 and revised in 1983, the instrument is used to assess physical pain in people who are communicative, responsive, and aged three years and older. The scale consists of faces ranging from "Face 0= no hurt" to "Face 10=hurts worst".
The Children's State Anxiety Scale (CSA): Developed by Ersig et al. (2013), the Turkish validity-reliability study of this visual scale was conducted by Özalp-Gerçeker et al. (2018) and it is scored from 0 to 10. Higher values represent higher anxiety.
The Children's Fear Scale (CFS): The instrument assessed the pain-associated fear in children. Developed by McMurty et al. (2011), the Turkish validity-reliability study of this visual scale was conducted by Özalp-Gerçeker et al. (2018) and it is scored from 0 to 4. It ranges from a no fear (neutral) face (0) on the far left to a face showing extreme fear on the far right. Higher scores mean a worse outcome.
Bubble Blowing Toy: In the bubble blowing group, a two-piece toy was used that had a chamber containing diluted liquid soap, a pattern of cartoon characters and a special apparatus to generate bubbles when blown.
iPad mini: In the cartoon watching group, an iPad mini was used that had a (7.9 inch (diagonal) LED-backlit Multi-Touch display, 2048 x 1536 resolution with a density of 326 pixels per inch (ppi) with internet access.
Interventions: The invasive procedure room in the clinic was decorated with cartoon characters and ornaments on the walls. The intervention can be administered to only one child at a time in the room. In routine practice, the parental presence is supported during all invasive procedures performed on children. However, the nurses' uniforms have a print/pattern of cartoon characters in the routine practice. The room had the same characteristics for all children and their parents in terms of environmental conditions such as light, temperature, noise, and seat. Before the procedure, children's pain, anxiety, and fear were assessed after providing developmentally appropriate information. The parents were also informed about how to support their children. The same researchers performed the venipuncture (R2) and observational pain, anxiety, and fear assessments (R3) in all children. R2 and R3 are nurses with more than five years of experience in pediatrics and degrees in scientific fields.
Bubble Blowing: First, the physical comfort of the children was ensured in the invasive procedure room. Then, the children were instructed to take a deep breath through the nose and generate bubbles by slowly blowing into the special apparatus. The children's questions about the procedure and the process were answered in a developmentally appropriate manner. The children were allowed to choose a bubble blowing toy according to the printed cartoon characters. The children were supported by their parents in holding the chamber of the toy. The children started to blow bubbles 3 minutes before the procedure. The procedure and the bubble blowing intervention were terminated simultaneously. The bubble blowing toy was given to the children as a gift after the intervention.
Cartoon Watching: In the cartoon watching group, the cartoons that the children liked to watch were learned from the parents before the procedure. First, the physical comfort of the children was ensured in the invasive procedure room. The children were asked which cartoon they wanted to watch before the procedure. They started to watch the cartoon 3 minutes before the procedure. The children were supported by their parents in holding the tablet. The procedure and the cartoon watching intervention were terminated simultaneously.
Statistical Methods: The study data were analyzed using the statistical package for Social Sciences. The level of statistical significance was set at 0.05. The normality of the data was determined by the kurtosis and skewness coefficients, revealing that the scale scores were normally distributed. The data were presented as mean, standard deviation, confidence interval, frequency, and percentages. The similarities of demographic and clinical characteristics between the groups were analyzed by the Chi-square test. The mean scale scores of the groups were compared using the Independent Samples t-test.
Ethical Considerations: The study was granted approval by the clinical research ethics committee and written institutional permission by the hospital. Parents were informed about the procedure and that they could withdraw from the study at any time without explanation. Parents provided written consent and children verbal consent before the study.
- Conditions
- Pain, Anxiety, Fear, Child, Only
- Being tested
- Bubble Blowing, Cartoon Watching
- Keywords
- Nursing, Pain Management, Distraction, Children
- Medical subject headings
- Pain, Anxiety Disorders, Agnosia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Bubble BlowingBehavioural
Active Distraction Methods
Cartoon WatchingBehavioural
Passive Distraction Methods
| Study group | Role | What they receive |
|---|---|---|
| Bubble Group | Experimental | The children started to blow bubbles 3 minutes before the procedure. The procedure and the bubble blowing intervention were terminated simultaneously. Receives: Behavioral: Bubble Blowing |
| Cartoon Group | Experimental | The children started to watch the cartoon 3 minutes before the procedure. The children were supported by their parents in holding the tablet. The procedure and the cartoon watching intervention were terminated simultaneously. Receives: Behavioral: Cartoon Watching |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pain assesed by Wong-Baker FACES
The Wong-Baker FACES (WB-FACES) Pain Rating Scale used. This scale uses in children aged 3 and older to rate pain severity. This numeric rating scale ranges from 0 to 10. Faces show emotions from smiling (0 = very happy/ no pain) to crying (10 = hurts worst).
Measured: Procedure (during the venipuncture)
Anxiety assesed by Children's State Anxiety Scale
The Children's State Anxiety Scale assesses children's anxiety. This scale is drawn like a thermometer with a bulb at the bottom and also includes horizontal lines at intervals going up to the top (0-10). This scale ranges from 0 to 10. Higher values represent higher anxiety.
Measured: Procedure (during the venipuncture)
Fear by Children's Fear Scale
The Child Fear Scale was used.This one-item scale measures procedure-related fear in children, consists of five sex-neutral faces, ranges from 0 (no fear) to 4 (extreme fear). Higher scores mean a worse outcome.
Measured: Procedure (during the venipuncture)
Secondary outcomes (3)
Pain assesed by Wong-Baker FACES
The Wong-Baker FACES (WB-FACES) Pain Rating Scale used. This scale uses in children aged 3 and older to rate pain severity. This numeric rating scale ranges from 0 to 10. Faces show emotions from smiling (0 = very happy/ no pain) to crying (10 = hurts worst).
Measured: After procedure (at 3rd minutes after the venipuncture)
Anxiety assesed by Children's State Anxiety Scale
The Children's State Anxiety Scale assesses children's anxiety. This scale is drawn like a thermometer with a bulb at the bottom and also includes horizontal lines at intervals going up to the top (0-10). This scale ranges from 0 to 10. Higher values represent higher anxiety.
Measured: After procedure (at 3rd minutes after the venipuncture)
Fear by Children's Fear Scale
The Child Fear Scale was used.This one-item scale measures procedure-related fear in children, consists of five sex-neutral faces, ranges from 0 (no fear) to 4 (extreme fear). Higher scores mean a worse outcome.
Measured: After procedure (at 3rd minutes after the venipuncture)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Dec 2021
- Study start15 Oct 2019
- Primary completion2 Mar 2020
- Study completion2 Mar 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for PainStudies of the same condition, open and under way.
- More trials run by Mersin 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 56 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mersin University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Guzide UGUCU, Mersin University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05161416
- Sponsor's protocol ID
- MersinU*GUGUCU_001
- Status last verified
- Sep 2024
- First submitted
- 5 Dec 2021
- Last updated
- 19 Sep 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There is not a plan to make IPD available due to ethical considerations.
Publications
Ugucu G, Akdeniz Uysal D, Guzel Polat O, Artuvan Z, Polat Kulcu D, Aksu D, Gulgun Altintas M, Cetin H, Orekici Temel G. Effects of cartoon watching and bubble-blowing during venipuncture on pain, fear, and anxiety in children aged 6-8 years: A randomized experimental study. J Pediatr Nurs. 2022 Jul-Aug;65:e107-e114. doi: 10.1016/j.pedn.2022.03.016. Epub 2022 Apr 8.
PubMed 35410736
Study at a glance
From the registry record, last updated by the sponsor on 19 Sep 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of the Effects of Cartoon Watching and Bubble Blowing as Distraction Methods During Venipuncture on Pain, Fear, and Anxiety in Children Aged 6-8 Years: A Randomized Experimental Study
- ClinicalTrials.gov ID
- NCT05161416
- Acronym / sponsor ID
- MersinU*GUGUCU_001
- Conditions
- Pain, Anxiety, Fear, Child, Only
- Keywords
- Nursing, Pain Management, Distraction, Children
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 56 participants (actual)
- Lead sponsor
- Mersin UniversityUniversity, hospital or other
- Study start
- 15 Oct 2019 (actual)
- Primary completion
- 2 Mar 2020 (actual)
- Study completion
- 2 Mar 2020 (actual)
- First posted
- 17 Dec 2021 (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.
Active and passive distraction methods are frequently used in the nursing management of procedural pain in children. There are no studies comparing the effects of cartoon watching (passive) and bubble blowing (active) as distraction methods on pain, anxiety, and fear associated with venipuncture in children.
This study aimed to compare the effects of bubble blowing (active distraction) and cartoon watching (passive distraction) techniques on pain, anxiety, and fear during venipuncture in children aged 6-8 years.
Detailed description
Research Hypotheses H1a= There is a difference in the mean WB-FACES score during the procedure between the bubble group (BG) and the cartoon group (CG).
H1b= There is a difference in the mean WB-FACES score after the procedure between the BG and CG groups.
H2a= There is a difference in the mean CSA score during the procedure between the BG and CG groups.
H2b= There is a difference in the mean CSA score after the procedure between the BG and CG groups.
H3a= There is a difference in the mean CFS score during the procedure between the BG and CG groups.
H3b= There is a difference in the mean CFS score after the procedure between the BG and CG groups.
Design and Settings: This parallel-group randomized trial was conducted at the invasive procedure room of the pediatrics department of a university hospital in the East Mediterranean Region of Turkey. For this experimental research, 56 children aged 6-8 years were assigned to two groups (Bubble Group=BG; n = 28 and Cartoon Group=CG; n = 28) using block randomization.
Sample Size: The main trial sample was calculated based on the pilot study findings. The pilot study was conducted with 20 children (BG; n = 10 and CG; n = 10) who met the eligibility criteria. A priori power analysis was performed based on the effect size (d = 0.885, large effect) of the difference in pain scores between the groups (during the procedure) determined in the pilot study. Using G*Power 3.1.9.7, the minimum sample size was calculated as 56 children, with 28 children per group, for a two-tailed hypothesis, an effect size of d = 0.885, an allocation ratio of n1/n2=1, type I error of 0.05, and a power of 90%.
Randomization: Using block randomization, six different combinations of the codes A and B with a block size of 4 (ABAB(1), AABB(2), BABA(3) …) were generated. The combinations were numbered from 1 to 6. The numbers (1-6) were randomly sorted 14 times via randomizer.org and a random allocation sequence was generated. Coin flipping was used to determine which of the codes A and B would be BG and CG (R1). The random allocation sequence, which was placed in opaque envelopes by giving a sequence number, was hidden from the principal researchers (R2, R3) (allocation concealment). The opaque envelopes were stored in a locked cabinet by the researcher who performed the randomization (R1). The group including the eligible children was not shared with R2 and R3 until the intervention.
Data Collection Tools Socio-Demographic Data Collection and Procedure Follow-up Form: It includes "age, gender, previous experience of hospitalization, experience of procedural pain in last week, analgesic administration at least six hours before the procedure, size of peripheral IV needle, area of IV blood sample, parental presence during procedure, and baseline data of pain, anxiety and fear scores of children before procedure".
The Wong-Bakers FACES® Pain Rating Scale (WB-FACES): Developed by Wong and Baker in 1981 and revised in 1983, the instrument is used to assess physical pain in people who are communicative, responsive, and aged three years and older. The scale consists of faces ranging from "Face 0= no hurt" to "Face 10=hurts worst".
The Children's State Anxiety Scale (CSA): Developed by Ersig et al. (2013), the Turkish validity-reliability study of this visual scale was conducted by Özalp-Gerçeker et al. (2018) and it is scored from 0 to 10. Higher values represent higher anxiety.
The Children's Fear Scale (CFS): The instrument assessed the pain-associated fear in children. Developed by McMurty et al. (2011), the Turkish validity-reliability study of this visual scale was conducted by Özalp-Gerçeker et al. (2018) and it is scored from 0 to 4. It ranges from a no fear (neutral) face (0) on the far left to a face showing extreme fear on the far right. Higher scores mean a worse outcome.
Bubble Blowing Toy: In the bubble blowing group, a two-piece toy was used that had a chamber containing diluted liquid soap, a pattern of cartoon characters and a special apparatus to generate bubbles when blown.
iPad mini: In the cartoon watching group, an iPad mini was used that had a (7.9 inch (diagonal) LED-backlit Multi-Touch display, 2048 x 1536 resolution with a density of 326 pixels per inch (ppi) with internet access.
Interventions: The invasive procedure room in the clinic was decorated with cartoon characters and ornaments on the walls. The intervention can be administered to only one child at a time in the room. In routine practice, the parental presence is supported during all invasive procedures performed on children. However, the nurses' uniforms have a print/pattern of cartoon characters in the routine practice. The room had the same characteristics for all children and their parents in terms of environmental conditions such as light, temperature, noise, and seat. Before the procedure, children's pain, anxiety, and fear were assessed after providing developmentally appropriate information. The parents were also informed about how to support their children. The same researchers performed the venipuncture (R2) and observational pain, anxiety, and fear assessments (R3) in all children. R2 and R3 are nurses with more than five years of experience in pediatrics and degrees in scientific fields.
Bubble Blowing: First, the physical comfort of the children was ensured in the invasive procedure room. Then, the children were instructed to take a deep breath through the nose and generate bubbles by slowly blowing into the special apparatus. The children's questions about the procedure and the process were answered in a developmentally appropriate manner. The children were allowed to choose a bubble blowing toy according to the printed cartoon characters. The children were supported by their parents in holding the chamber of the toy. The children started to blow bubbles 3 minutes before the procedure. The procedure and the bubble blowing intervention were terminated simultaneously. The bubble blowing toy was given to the children as a gift after the intervention.
Cartoon Watching: In the cartoon watching group, the cartoons that the children liked to watch were learned from the parents before the procedure. First, the physical comfort of the children was ensured in the invasive procedure room. The children were asked which cartoon they wanted to watch before the procedure. They started to watch the cartoon 3 minutes before the procedure. The children were supported by their parents in holding the tablet. The procedure and the cartoon watching intervention were terminated simultaneously.
Statistical Methods: The study data were analyzed using the statistical package for Social Sciences. The level of statistical significance was set at 0.05. The normality of the data was determined by the kurtosis and skewness coefficients, revealing that the scale scores were normally distributed. The data were presented as mean, standard deviation, confidence interval, frequency, and percentages. The similarities of demographic and clinical characteristics between the groups were analyzed by the Chi-square test. The mean scale scores of the groups were compared using the Independent Samples t-test.
Ethical Considerations: The study was granted approval by the clinical research ethics committee and written institutional permission by the hospital. Parents were informed about the procedure and that they could withdraw from the study at any time without explanation. Parents provided written consent and children verbal consent before the study.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Bubble Group | Experimental | Behavioral: Bubble BlowingThe children started to blow bubbles 3 minutes before the procedure. The procedure and the bubble blowing intervention were terminated simultaneously. |
| Cartoon Group | Experimental | Behavioral: Cartoon WatchingThe children started to watch the cartoon 3 minutes before the procedure. The children were supported by their parents in holding the tablet. The procedure and the cartoon watching intervention were terminated simultaneously. |
Who may qualify
- Ages
- 6 to 8 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- Child aged 6-8 years
- Child with need or plan for venipuncture (antecubital fossa)
Key exclusion criteria (2 listed)
- Child with a neurodegenerative disease, mental retardation, vision and hearing problems, chronic, life-threatening (sepsis, shock, respiratory / cardiac arrest) or genetic disease
- Child with use of opioids, narcotics, analgesics or sedatives in the last 24 hours before the procedure
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 |
|---|---|---|
| Bubble BlowingActive Distraction Methods | Behavioural | Bubble Group |
| Cartoon WatchingPassive Distraction Methods | Behavioural | Cartoon Group |
Primary outcome
Pain assesed by Wong-Baker FACES
Time frame: Procedure (during the venipuncture)
The Wong-Baker FACES (WB-FACES) Pain Rating Scale used. This scale uses in children aged 3 and older to rate pain severity. This numeric rating scale ranges from 0 to 10. Faces show emotions from smiling (0 = very happy/ no pain) to crying (10 = hurts worst).
Anxiety assesed by Children's State Anxiety Scale
Time frame: Procedure (during the venipuncture)
The Children's State Anxiety Scale assesses children's anxiety. This scale is drawn like a thermometer with a bulb at the bottom and also includes horizontal lines at intervals going up to the top (0-10). This scale ranges from 0 to 10. Higher values represent higher anxiety.
Fear by Children's Fear Scale
Time frame: Procedure (during the venipuncture)
The Child Fear Scale was used.This one-item scale measures procedure-related fear in children, consists of five sex-neutral faces, ranges from 0 (no fear) to 4 (extreme fear). Higher scores mean a worse outcome.
3 secondary outcomes
Pain assesed by Wong-Baker FACES
Time frame: After procedure (at 3rd minutes after the venipuncture)
Anxiety assesed by Children's State Anxiety Scale
Time frame: After procedure (at 3rd minutes after the venipuncture)
Fear by Children's Fear Scale
Time frame: After procedure (at 3rd minutes after the venipuncture)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Sep 2024.
- Results publication: PubMed 35410736Ugucu G, Akdeniz Uysal D, Guzel Polat O, Artuvan Z, Polat Kulcu D, Aksu D, Gulgun Altintas M, Cetin H, Orekici Temel G. Effects of cartoon watching and bubble-blowing during venipuncture on pain, fear, and anxiety in children aged 6-8 years: A randomized experimental study. J Pediatr Nurs. 2022 Jul-Aug;65:e107-e114. doi: 10.1016/j.pedn.2022.03.016. Epub 2022 Apr 8.
- Individual participant dataSharing planned: No. There is not a plan to make IPD available due to ethical considerations.
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Bubble Blowing and Cartoon Watching in people with Pain and Anxiety, run by Mersin 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 2 inclusion and 2 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: finished, as of the sponsor's last update on 19 Sep 2024. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Pain assesed by Wong-Baker FACES (time frame: Procedure (during the venipuncture)). The study lists 3 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 NCT05161416, which also lists 1 linked publication.
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 19 Sep 2024.