NCT06008496

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
7,839

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 2, 2023

Completed
4 months until next milestone

First Posted

Study publicly available on registry

August 23, 2023

Completed
5 months until next milestone

Study Start

First participant enrolled

January 15, 2024

Completed
25 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 9, 2024

Completed
1.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
Last Updated

July 30, 2025

Status Verified

July 1, 2025

Enrollment Period

25 days

First QC Date

May 2, 2023

Last Update Submit

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

Age18 Years - 110 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

University Hospitals Plymouth NHS Trust

Plymouth, Devon, United Kingdom

Location

MeSH Terms

Conditions

PainPain, PostoperativeChronic Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsPostoperative ComplicationsPathologic Processes

Study Officials

  • Mark Rockett, MBBS, PhD

    University Hospitals Plymouth NHS Trust

    STUDY DIRECTOR

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

Locations