Oslo University Hospital
Oslo, 0424, Norway
NCT Number: NCT03987399
This study will explore healthcare providers' pediatric postoperative pain management knowledge and clinical practice. The aim of this study is to explore healthcare providers' knowledge and clinical practice in pediatric postoperative pain management in surgical wards, and to evaluate whether an educational intervention would improve postoperative pain management. This study has a pre-post intervention design. This study will be conducted on four surgical wards in one university hospital in Norway. There will be used different methodological approaches for data collections (interviews, questionnaire, observational study) with four measurement points; baseline (T1), and one month (T2), six months (T3) and 12 months (T4) after intervention.
This study is active but is not currently recruiting participants.
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Interventional
Not applicable
Oslo, 0424, Norway
This study will be conducted on four surgical wards in one university hospital in Norway. There will be used different methodological approaches for data collections (interviews, questionnaire, observational study) with four measurement points; baseline (T1), and one month (T2), six months (T3) and 12 months (T4) after intervention.
To get a broader view of barriers and facilitators for effective pediatric postoperative pain management, there will be carried out focus group interviews with healthcare providers. Further, data about healthcare providers' knowledge and attitudes regarding pediatric pain will be collected using a questionnaire. Data about nurses' pediatric postoperative pain management will be collected using non-participant observational study and data about children's experience about pain and pain management will be collected using face-to-face interviews with children. This study will have different phases:
Phase 1 Explore healthcare providers' knowledge, clinical practice children's experiences of pain and pain management, and healthcare providers' experiences of barriers and facilitators for effective pain management
Phase 2 Develop and implement a tailored educational intervention
Develop tailored educational intervention based on:
Implementation of the intervention
Phase 3 Evaluation of the intervention
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Questionnaire
Inclusion criteria
Exclusion criteria
Observational study
Inclusion criteria
Interview with children
Inclusion criteria
Exclusion criteria
Interview with healthcare providers
Inclusion criteria
Educational day (lecture and workshop), clinical supervision and reminders
Time frame: Baseline
Evaluated with "The Pediatric Nurses' Knowledge and Attitudes Survey Regarding Pain Questionnaire - Norwegian version" (PNKAS-N).The questionnaire consists of 36 questions with a total score of 36. The scale ranges from minimum 0 to maximum 36 (best score).
Time frame: short term - one month after intervention and long term - six and 12 months after intervention
Evaluated with "The Pediatric Nurses' Knowledge and Attitudes Survey Regarding Pain Questionnaire - Norwegian version" (PNKAS-N). The questionnaire consists of 36 questions with a total score of 36. The scale ranges from minimum 0 to maximum 36 (best score).
Time frame: Baseline
Evaluated with non-participant observation using a structured observational tool (checklist) and field notes
Time frame: short term - one month after intervention and long term - six and 12 months after intervention
Evaluated with non-participant observation using a structured observational tool (checklist) and field notes
Time frame: Baseline
Evaluated using semi-structured face-to-face interviews with children after surgery
Time frame: Baseline
Evaluated using semi-structured focus group interviews with healthcare providers
Oslo University Hospital
Other
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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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