Study design and setting
This study was designed as a cross-sectional study. The study was conducted in the primary care centres in Nablus. Nablus city was chosen as it is one of the largest cities in Palestine. The data was collected over a period of 3 months from June 2018 to 31 to August 2018.
Participants
The subjects of our study were selected from people who visited the children care clinic in the primary care centers in Nablus where parents routinely went to vaccinate their children and thus where we concentrated on the dates when the appropriate sample could be recruited. The samples were selected by convenience with inclusion criteria of parents aged more than 19, who had a child or more aged between 6 months and 10 years [21-24], and who agreed to participate in the study. Subjects with vision problems, cognitive/physical disabilities, and caregivers other than parents were excluded. Convenience sampling was used. A total of 434 parents were approached; however, we got a consent from 420 parents with a valid response of 96.8%.
Intervention (questionnaire)
The data was collected using a data collection questionnaire based on the relevant literature [11, 25-27]. The data collection form included four sections (Additional file 1).
The first section gathered demographic information including sex, residency, age, occupational status, marital status, educational level, monthly income and number of children between six months and ten years. The second section gathered information about drugs, including questions about who is responsible for administering medication at home, whether their child had ever refused to take tablets/pills, what was done when their child did not like taking tablet drugs, whether the treatment process failed because their child did not like taking tablet drugs, whether their child ever refused to take liquid medications, what was done when their child did not like taking liquid drugs, whether the treatment process failed because their child did not like taking liquid medications and the source of information for drugs given to their child.
The third section gathered information about the child, including questions about whether the child had difficulties in swallowing medication, the type of swallowing problem, how many times they complained about swallowing difficulties, whether swallowing difficulties were discussed with a doctor, and the doctor’s recommendations.
The fourth section gathered information about practices, including questions about the tool had you used for giving a child their prescribed liquid medications, whether the leaflet attached to the drug was read, whether the child was given a dose higher than that prescribed to treat them more quickly, whether the child was given more than one type of oral medication at the same time, whether the child was given medications without prescription from a doctor, the type of medications used, whether the time the drugs were given to the child were recorded, and what was done with any remaining drugs when the child had recovered. They were also asked for the hours at which they would give their child medicine if it had been prescribed for three times a day.
A pilot study was undertaken with 30 participants to check for necessary modifications in the questionnaire, but as the selected participants all understood the questionnaire, no modifications were made. The questionnaire was reviewed and evaluated by experts in the field of pharmacy practice to ensure its content validity.
Outcomes
The primary outcome of our study was a composite consisted of parents' practices during the administration of oral drugs to their children at home and the acceptance behaviors of their children. In addition, swallowing problems during the administration of these drugs were included in the composite outcome. As a secondary outcome, we reported the most commonly used self-therapies by parents for their children.
Sample size
An online Raosoft sample size calculator (http://www.raosoft.com/samplesize.html( was applied to determine the sample size, which was 377. By assuming a response distribution for parents or caregivers who faced problems and difficulties when administering oral drugs to their children at home was 50%. A confidence level of 95% and a 5% margin of error were used, adding a non-response rate of 10% to increase accuracy.
Statistics
The data was coded, categorised, and entered into the Statistical Package for the Social Sciences (SPSS), version 16.0. Descriptive statistics (e.g. frequency, percentage, mean, standard deviation) were used to illustrate the sociodemographic data and clinical data.
Ethics
Ethical approval for the study was obtained from institutional review board (IRB) at An-Najah National University. The questionnaire content was described before the interview, and verbal informed consent was taken from each parent before the interviews were started.