Key result
This is a study protocol for a stepped wedge cluster randomized controlled trial evaluating a standardized care pathway for atraumatic abdominal pain in the emergency department; no results are available yet.
Why the study?
The study was designed to improve emergency department care for patients presenting with atraumatic abdominal pain through a standardized, evidence-based pathway.
Does an app-supported standardized care pathway improve pain, treatment duration, and satisfaction in ED patients with atraumatic abdominal pain?
RCT (n=2,000)
Open-label
Cluster randomized (stepped wedge)
Yes
Does an app-supported standardized care pathway improve pain, treatment duration, and satisfaction in ED patients with atraumatic abdominal pain?
This study protocol describes a stepped wedge cluster randomized trial to evaluate a standardized, app-supported care pathway for patients with atraumatic abdominal pain in the emergency department.
Protocol published; leaves open whether app-supported pathway improves ED outcomes in atraumatic abdominal pain.
This study aims to improve emergency department (ED) care for patients suffering from atraumatic abdominal pain. An application-supported pathway for the ED will be implemented, which supports quick, evidence-based, and standardized diagnosis and treatment steps for patients with atraumatic abdominal pain at the ED. A mixed-methods multicentre cluster randomized controlled stepped wedge trial design will be applied. A total of 10 hospitals with EDs (expected n = 2.000 atraumatic abdominal pain patients) will consecutively (every 4 months) be randomized to apply the intervention. Inclusion criteria for patients are a minimum age of 18 years, suffering from atraumatic abdominal pain and being insured with a German statutory health insurance. Primary outcomes: acute pain score at time of discharge from ED, duration of treatment at the ED, patient-reported satisfaction. Secondary endpoints include patient safety and quality of care parameters, process evaluation parameters, and costs and cost-effectiveness parameters. Quantitative data will be gathered from patient-surveys, clinical records, and routine data from hospital information systems as well as from a participating German statutory health insurance. Descriptive and analytic statistical analysis will be performed to provide summaries and associations for primary patient-reported outcomes, process measures, quality measures, and costs. Qualitative data collection consists of participatory patient observations and semi-structured expert interviews, which will be inductively analysed. Findings will be disseminated in publications in peer-reviewed journals, on conferences, as well as via a project website. To ensure data protection, appropriate technical and organisational measures will be taken. Trial registration: DRKS00021052.
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Altendorf et al. (2022) conducted an RCT in Atraumatic abdominal pain (n=2,000). App-supported Abdominal Pain Unit (APU) care pathway vs. Care as usual was evaluated on Acute pain score at discharge, duration of treatment at the ED, and patient-reported satisfaction. This is a study protocol for a stepped wedge cluster randomized controlled trial evaluating a standardized care pathway for atraumatic abdominal pain in the emergency department; no results are available yet.
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