Case study 4
Aim of the case study To apply the pain review delivery framework flexibly with patients not ready to reduce their opioids To identify how listening to and acknowledging patients’ concerns …
Case study 3
Aim of the case study To identify how an understanding of what matters to the patient can be achieved (link back to spirit of PROMPPT) To describe how using reflections …
Case study 1
Aim of the case study To identify components of the pain review delivery framework in action To recognise a patient’s readiness to trial an opioid reduction To identify how the …
The PROMPPT Trial
The PROMPPT trial aims to test the effectiveness of the PROMPPT intervention (the training package, the pain review, patient facing information and documents) to reduce opioid use in patients prescribed …
Good Clinical Practice
GCP stands for good clinical practice and is an Internationally recognised standard for conducting a clinical trial. It enforces tight guidelines on ethical aspects of a clinical study High standards …
Safety Reporting
Patient safety is of paramount importance in clinical research and safety reporting is a critical part of the PROMPPT trial. The pain review is considered to be evidence-based best practice …
MOPP-2 Process Evaluation
When evaluating interventions, it is important to not only assess the effectiveness of the intervention but to also explore the reasons as to why and how it works or doesn’t …
Pain Reviews
In this section we will outline how you can go about scheduling pain reviews and give you some guidance on completing relevant study documents. It is anticipated that you will …
MOPP Questionnaire Study
The MOPP questionnaire study will ask participants from all GP practices involved in the trial to complete a baseline (with embedded consent), 3, 6 and 12 month questionnaire. The questionnaire …
