Pediatric Postoperative Pain Management in Surgical Wards - an Intervention Study
Last updated on July 2021Recruitment
- Recruitment Status
- Active, not recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Postoperative Pain
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care
Participation Requirements
- Age
- Younger than 125 years
- Gender
- Both males and females
Description
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 ...
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 Questionnaire PNKAS-N Observation of clinical practice Face-to-face interviews with children Focus group interviews with healthcare providers (barriers and facilitators) Phase 2 Develop and implement a tailored educational intervention Develop tailored educational intervention based on: Available research Results from baseline Feedback from head of the relevant units Staff views about the facilitators and barriers to optimized pediatric pain management Implementation of the intervention Seminar (lecture and workshop) Clinical supervision Reminders Phase 3 Evaluation of the intervention Questionnaire PNKAS-N Observation of clinical practice
Tracking Information
- NCT #
- NCT03987399
- Collaborators
- Karolinska University Hospital
- Investigators
- Principal Investigator: Morten C Moe, PhD Oslo University Hospital
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