None listed
Conditions
Brief summary
This research project is called "Personalised advice and instructions for pain relief following discharge from ED". This research project is aiming to study the ways doctors and nurses to give pain relief instructions to patients who are being discharged from the emergency department. We are particularly interested in whether personalising the pain relief instructions and making them print outs and accessible on mobile phone is useful for patients. We aim to use the information from this research to improve the ways we provide pain relief instructions to patients leaving the emergency department.
Interventions
Pain has been suggested to be the "fifth vital sign", of obvious importance to the patient. Many patients who present to Emergency Departments are discharged home with pain, and need to take analgesia after discharge. This study aims to understand whether personalised advice provided to patients improves their compliance with medications, pain scores and understanding following discharge. The PAIN study will be run as a prospective randomised controlled trial at the Sir Charles Gairdner Hospital Emergency Department. This is a pilot study. All patients who present with pain will be assessed for suitability, and if satisfying the inclusion and exclusion criteria, will be invited to participate in the study. This will involve randomisation to the control group who will receive the usual pain relief instructions or the intervention group who will receive customised pain relief instructions as a print out and via their mobile phone. The instructions are created via a web/mobile application and combine small sections of advice in simple, readable text with accompanying pictograms. These instructions are customised for each patient based on the pain relief advice given to them at discharge by their treating doctor. The content of the print out of the instructions is viewable by text message (in the exact same format) on the patient's phone at discharge. All patients will be followed up at 5 days with an online questionnaire.
Sponsors
Study design
Eligibility
Inclusion criteria
• acute musculoskeletal complaints not requiring admissions (strains, sprains, extremity fractures not requiring operative management, gouty arthritis) or • visceral complaints not requiring admission (abdominal pain, renal colic, gynaecological pain with negative pregnancy test, or biliary colic).
Exclusion criteria
• need for admission or observation • unwilling or unable to comply with follow up • non-English speaking • a prisoner • fracture requiring surgery • chronic pain syndrome • clinical suspicion of drug-seeking behaviour