This study was a randomized controlled clinical trial with intervention and control groups, aimed at determining the effect of watching cartoons on pain and anxiety due to venipuncture in children aged 3 - 6 years admitted to the pediatric ward of Bu-Ali Sina Hospital in Sari, Iran, between March 2021 and 2022. Inclusion criteria included the need for an IV-line, age between 37 and 72 months, awareness and ability to communicate, the presence of a parent with the child, informed consent to participate, and the child's interest in watching cartoons. Exclusion criteria included parents being health professionals, the child having speech and hearing impairments, mental retardation, seizures, or other life-threatening conditions, failure of the first venipuncture attempt, venous access obtained in a different area, and use of an angiocatheter other than No. 24.
The sample size was calculated to be 140 cases (70 in the intervention group and 70 in the control group) with a 95% confidence level and 90% power based on the study by Sadeghi and Raeisi (
11). Eligible children were randomly assigned to the intervention and control groups using Random Bit Excel software.
Before venipuncture, the demographic and medical information of the children was recorded, including gender, age, birth order, place of residence, parents' education level and occupation, reason for admission, presence of acute pain due to illness, receipt of analgesics (acetaminophen, ibuprofen, diclofenac) within 4 hours before venipuncture, history of anxiety disorder and use of anti-anxiety medications (fluoxetine and sertraline), presence of anxiety disorder based on the Preschool Anxiety Scale, history of kindergarten attendance, and history of previous venipuncture. This information was collected by the researcher through an interview before the venipuncture procedure (
Table 1).
| Variables | Intervention | Control | P-Value |
|---|
| Gender | | | 1 |
| Boy | 39 (55.7) | 39 (55.7) | |
| Girl | 31 (44.3) | 31 (44.3) | |
| Birth order | | | 0.282 |
| 1 | 36 (51.4) | 45 (64.3) | |
| 2 | 31 (44.3) | 22 (31.4) | |
| ≤ 3 | 3 (4.3) | 3 (4.3) | |
| Mother’s education | | | 0.905 |
| Lower than high school | 10 (14.3) | 13 (18.6) | |
| Diploma | 28 (40) | 30 (42.9) | |
| Post diploma | 5 (7.1) | 5 (7.1) | |
| Bachelor | 21 (30) | 15 (21.4) | |
| Master | 4 (5.7) | 5 (7.1) | |
| PhD | 2 (2.9) | 2 (2.9) | |
| Father’s education | | | 0.565 |
| Lower than high school | 10 (14.3) | 12 (17.1) | |
| Diploma | 37 (52.9) | 37 (52.9) | |
| Post diploma | 3 (4.3) | 5 (7.1) | |
| Bachelor | 13 (18.6) | 10 (14.3) | |
| Master | 7 (10) | 4 (5.7) | |
| PhD | 0 (0) | 2 (2.9) | |
| Mother’s job | | | 0.494 |
| Non-employee | 2 (2.9) | 3 (4.3) | |
| Employee | 6 (8.6) | 10 (14.3) | |
| Housewife | 62 (88.6) | 57 (81.4) | |
| Father’s job | | | 0.311 |
| Non-employee | 51 (72.9) | 44 (62.9) | |
| Employee | 19 (27.1) | 25 (35.7) | |
| Jobless | 0 (0) | 1 (1.4) | |
| Location | | | 0.515 |
| Urban | 59 (84.3) | 55 (78.6) | |
| Rural | 11 (15.7) | 15 (21.4) | |
| History of kindergarten | | | 0.097 |
| Yes | 2 (2.9) | 8 (11.4) | |
| No | 68 (97.1) | 62 (88.6) | |
| History of venipuncture | | | 0.306 |
| Yes | 34 (48.6) | 27 (38.6) | |
| No | 36 (51.4) | 43 (61.4) | |
| History of pain relief | | | 0.801 |
| Yes | 8 (11.4) | 10 (14.3) | |
| No | 62 (88.6) | 60 (85.7) | |
| Reason for admission | | | 0.176 |
| COVID-19 | 32 (45.7) | 40 (57.1) | |
| Other | 38 (54.3) | 30 (42.9) | |
| Average ranks; (sum of ranks) | | | |
| Anxiety disorder score based on PAS scale | 70.34 (4923.50) | 70.66 (4946.50) | 0.955 |
| Duration of venipuncture | 68.73 (4811.0) | 72.27 (5059.0) | 0.605 |
a Values are expressed as No. (%).
The Preschool Anxiety Scale, designed by Spence and colleagues in 2001, was used to assess pre-procedure anxiety. This scale, based on the DSM-IV anxiety disorders list and completed by parents (
18), includes 28 questions (excluding those on post-traumatic stress disorder) and covers five areas: Generalized anxiety, social phobia, separation anxiety, fear of physical injury, and obsession (
19). Scores range from 0 to 112, with scores between 0 and 37 indicating low anxiety, 37 to 75 indicating moderate anxiety, and above 75 indicating high anxiety (
20). Psychometric evaluation of the scale shows moderate to good internal validity (Cronbach's alpha > 0.7). The correlation between information from mothers and fathers was greater than 0.6, and the test-retest correlation (over 12 months) was also higher than 0.6 (
21).
The FLACC (face, legs, activity, cry, and consolability) behavioral pain scale was used to measure pain during venipuncture. This scale includes five components: Facial expression, leg movement, activity level, crying, and consolability, each scored as 0, 1, or 2 by the main researcher. The scores from each component are summed to provide a total score. A score of 0 - 3 indicates mild pain, 4 - 6 indicates moderate pain, and 7 - 10 indicates severe pain. A score of 0 represents no pain, while a score of 10 represents the highest level of pain. In the study by Sadeghi et al., the content validity of this scale was confirmed by seven university professors, and its reliability was established by applying the tool to 20 children and using a FACES Scale (r = 0.707) (
22).
The Facial Image Scale (FIS) was used to assess anxiety caused by venipuncture. This scale features a row of five faces, numbered from 1 to 5, ranging from very happy (score of 1) to very unhappy (score of 5). Children were asked to point to the face that best reflected their feelings at that moment. This tool has been psychometrically tested for children ages 3 to 18 years and has been employed in various studies to measure anxiety in children (
23-
26). The psychometric validity of this tool has been confirmed in multiple studies (
27,
28).
Sampling continued until the desired sample size was reached. After providing complete oral information about the purpose and method of the study, written informed consent was obtained from the child's parent or guardian. Before venipuncture, demographic and medical questionnaires were completed, and the presence of anxiety disorder in the child was assessed using the FIS and recorded by a researcher. If necessary, at the discretion of the treating physician, a visit with a child psychiatrist was conducted in the hospital.
To prevent separation anxiety, children were accompanied by a parent in the venipuncture room. Venipuncture was performed on the back of the hand using a No. 24 angiocatheter by expert nurses with over two years of clinical experience in the pediatric ward. The catheter was inserted at a 25 - 30-degree angle for all venipunctures. For the control group, routine methods such as talking were used. For the intervention group, in addition to the usual methods, a distraction technique (watching cartoons) was employed. The "Pooches Family" cartoon is an informative and engaging animated series designed for children and young audiences. It features a family of seven dogs who have interesting adventures in each episode. The cartoon, suitable for children aged 2 to 10, is known for its cheerful atmosphere and high appeal, making it effective in capturing children's attention and teaching life lessons. This cartoon has been translated into Persian and is broadcast on Iranian television and media. Prior to the procedure, the "Pooches Family" cartoon (duration = 4 minutes and 33 seconds) was shown to the intervention group using a tablet. The cartoon was shown to the control group after the venipuncture.
Anxiety due to venipuncture in both groups was assessed and recorded using the FIS scale immediately before and after venipuncture by a researcher. Additionally, pain due to venipuncture in both groups was measured and recorded using the FLACC Scale immediately before and after the procedure. Finally, the pain and anxiety levels in the two groups were compared.
3.1. Data Analysis
After collecting data and presenting descriptive statistics, data analysis was conducted. To ensure the similarity of the two groups, a t-test was used for quantitative variables, and a chi-square test was used for qualitative variables. Since pain and anxiety scores were not normally distributed based on the Kolmogorov-Smirnov test (P < 0.05), the Mann-Whitney U test was applied to compare the mean pain and anxiety ranks before and after venipuncture between the intervention and control groups. The Wilcoxon signed ranks test was used to compare pain levels before and after venipuncture within each group. Children who completed the study were analyzed according to the protocol. In this research, the significance level was set at less than 0.05, and data analysis was performed using SPSS software version 20.0.
This project was approved by the Ethics Committee of Mazandaran University of Medical Sciences (
IR.MAZUMS.REC.1399.735) and registered in the Iranian Registry of Clinical Trials (
IRCT20171203037723N5). Informed consent was obtained from parents both verbally and in writing, and they were assured of privacy and confidentiality.