Patient Reported Outcomes, Postoperative Pain and Pain Relief After Day Case Surgery (POPPY)
POPPY
The POPPY Study: Patient Reported Outcomes, Postoperative Pain and Pain Relief After Day Case Surgery
1 other identifier
observational
7,839
1 country
1
Brief Summary
Around 3 out of 4 operations in the UK are performed as day-case, meaning the patient goes home on the same day of their operation. Hospitals usually do not follow up patients after day-case operations so we do not know very much about their short or long-term recovery. Some patients, even those who have had small operations, can develop persistent pain afterwards that continues for a long time (months to years). These patients may end up taking strong painkillers for a long time and this risks serious side effects and long-term health problems. The POPPY study aims to find out what recovery from day-case operations is like from the patient's point of view. We will look at the first week after patients' operations and then at 3 months to see if they are in pain, and if so what pain relief they are taking. All adults over the 5-day study period having day-case operations in the UK, with an anaesthetist, will be eligible if they have access to a smartphone. Patients will be recruited on the day of their operation from over 100 NHS hospitals. Some relevant information about the patient's current health, operation and anaesthetic will be recorded from their notes. Afterwards participants will get a text message at days 1, 3 and 7 and the at 3 months. These will connect to a data secure online questionnaire about pain, recovery, and what medications they are taking. A small number of participants with ongoing pain at 3 months will be invited to take part in a structured interview to understand their experience in more depth. This study will provide important information that may be used to improve care of patients having day-case operations and plan future research studies aimed to prevent persistent pain and long-term use of strong painkillers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 2, 2023
CompletedFirst Posted
Study publicly available on registry
August 23, 2023
CompletedStudy Start
First participant enrolled
January 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 9, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedJuly 30, 2025
July 1, 2025
25 days
May 2, 2023
July 29, 2025
Conditions
Outcome Measures
Primary Outcomes (3)
To measure short and long-term patient reported outcomes in UK day-case surgery patients.
See below outcomes for specifics (this is an overarching outcome which is broken down in the outcomes described below).
3 months
Short-term: to describe the quality of recovery over the first postoperative week
QOR-15 score (quality of recovery-15 score); BPI (brief pain inventory) derived pain scores; FPS (functional pain score)
1 week
Long-term: to establish the prevalence of persistent postsurgical pain (PPSP) and persistent postoperative opioid use (PPOU) in day case surgical patients.
PPOU prevalence (from medication use); pain at surgical site questionnaire; GAD-7 Score (generalised anxiety and depression 7 score); EQ-5D-5L score; BPI score; PHQ-8 Score (Patient Health Questionnaire 8)
3 months
Secondary Outcomes (6)
To identify those patient, medication, anaesthetic, and surgical characteristics that are associated with poor quality of recovery, and PPSP and/or PPOU
3 months
To describe the acute pain experience and analgesia use in the first postoperative week
1 week
To estimate the need for further healthcare support in the first postoperative week
1 week
To determine the patient reported acceptability of SMS prompted follow-up
1 week
To determine the difference in quality of life between participants with and without PPSP
3 months
- +1 more secondary outcomes
Other Outcomes (1)
To explore patient experience of; Preparation for day case surgery and pre-operative expectations Acute recovery (first postoperative week) Longer-term recovery and post-operative pain (after 3 months) Opioids: intake, type, duration and experience.
4-5 months
Interventions
Operation, surgical group, magnitude of surgery, anaesthetic type.
Eligibility Criteria
Adults undergoing day-case surgery in the UK
You may qualify if:
- Aged 18 years or older on day of surgery
- Day-case surgery as defined by National Day Surgery Delivery Pack (NEED REF)
- An anaesthetist must be present for case.
- The procedure must involve one or more of: sedation, regional anaesthesia, central neuraxial anaesthesia or general anaesthesia
You may not qualify if:
- Less than 18 years of age on day of surgery
- No anaesthetist involved with the procedure (such as local anaesthesia provided by a surgeon)
- Overnight stay (admission to hospital)
- Participant lacking capacity for consent
- Diagnostic and/or minimally invasive procedures (e.g., radiology, endoscopy, or cardiology procedures)
- Currently breast feeding
- Ophthalmic procedures
- No access to Smartphone and email
- Prisoners
- Eligibility for qualitative component:
- As above, plus reporting PPSP and/or PPOU at day 97 post operative
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital Plymouth NHS Trustlead
- National Institute for Academic Anaesthesiacollaborator
- Newcastle PROMScollaborator
- Research and Audit Federation of Anaesthetic Trainees (RAFT)collaborator
- University of Plymouthcollaborator
Study Sites (1)
University Hospitals Plymouth NHS Trust
Plymouth, Devon, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Mark Rockett, MBBS, PhD
University Hospitals Plymouth NHS Trust
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 2, 2023
First Posted
August 23, 2023
Study Start
January 15, 2024
Primary Completion
February 9, 2024
Study Completion
July 1, 2025
Last Updated
July 30, 2025
Record last verified: 2025-07