Dogubayazit State Hospital
Ağrı, Dogubeyazit, 04400, Turkey (Türkiye)
NCT Number: NCT07381673
This study aims to examine the relationship between parental self-efficacy in supporting child autonomy and postoperative pain levels in children undergoing minor surgical procedures. The study will be conducted with children aged 3 to 18 years and their parents at a single hospital in Turkey.Participation in the study is voluntary. Parents will be asked to complete questionnaires assessing their confidence in supporting their child's autonomy during the surgical process. Children's postoperative pain levels will be assessed using an age-appropriate pain rating scale during the early postoperative period.No experimental treatment or additional medical procedures will be performed as part of this study. All data will be collected as part of routine care and questionnaire assessments. The results of this study are expected to contribute to improved family-centered perioperative care for children undergoing minor surgery.
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Notify Me3 year–18 year
All sexes
Observational
Ağrı, Dogubeyazit, 04400, Turkey (Türkiye)
This prospective observational study is designed to investigate the relationship between parental self-efficacy for supporting child autonomy and postoperative pain levels in children undergoing minor surgical procedures.
The study population consists of children aged 3 to 18 years who are scheduled for minor surgery and their parents or legal guardians. Data will be collected at a single tertiary-level state hospital in Turkey. Participation is based on voluntary informed consent obtained from parents, and age-appropriate assent will be obtained from children when applicable.
Parental self-efficacy related to supporting child autonomy during the surgical process will be assessed preoperatively using the Parental Self-Efficacy Scale for Child Autonomy Toward Minor Surgery, a validated questionnaire. Postoperative pain intensity in children will be assessed during the early postoperative period using the Wong-Baker FACES Pain Rating Scale at predefined time points.
No interventions beyond standard clinical care will be implemented as part of the study. The study does not involve the use of investigational drugs, devices, or experimental procedures. All clinical care, including pain management, will be provided according to routine hospital protocols.
Descriptive statistics will be used to summarize participant characteristics and scale scores. The relationship between parental self-efficacy and postoperative pain levels will be analyzed using appropriate correlational and regression-based statistical methods. The findings are expected to support the development of family-centered perioperative nursing approaches aimed at improving postoperative pain outcomes in children undergoing minor surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: At 0, 2, and 6 hours after surgery
Postoperative pain intensity measured using the Wong-Baker FACES Pain Rating Scale, scored from 0 (no pain) to 10 (severe pain). Pain assessments will be conducted at multiple predefined time points during the early postoperative period.
Time frame: Preoperative period, prior to surgery
Parental self-efficacy assessed using the Parental Self-Efficacy Scale for Child Autonomy Toward Minor Surgery, an 18-item Likert-type scale with scores ranging from 1 to 4, where higher total scores indicate higher parental self-efficacy.
Agri Ibrahim Cecen University
Other
The Effect of Parental Self-Efficacy for Child Autonomy on Postoperative Pain in Children Undergoing Minor Surgery
Acronym: PSE-PAIN-MS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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