Exploring if Patients Can Safely and Easily Swab Their Own Surgical Wounds at Home

NCT07200401 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-01-09

No results posted yet for this study

Summary

The goal of this observational feasibility study is to learn if patients can safely, acceptably, and effectively collect their own wound swabs at home to detect clinically significant organisms in adults aged 18 and over who have had cardiac surgery via median sternotomy (central chest wound). Participants will be recruited from two sites: Harefield Hospital (Guy's and St Thomas' NHS Foundation Trust, London) and the Royal Sussex County Hospital (University Hospitals Sussex, Brighton).

The main questions it aims to answer are:

* Can home-based patient self-swabbing of surgical wounds provide swabs of sufficient quality for microbiological testing?
* Is self-swabbing at home safe and acceptable to patients following cardiac surgery?
* Could this approach be a cost-effective way to monitor for surgical wound infections?

Participants will:

* Receive a co-designed self-swabbing instruction pack, created in collaboration with a patient and public working group and clinical experts.
* Be observed via Microsoft Teams by a research practitioner while self-swabbing (or having their carer do so) to assess usability and adherence to instructions.
* Participate in a brief interview to share their experiences and feedback on the instructions and swabbing process.
* Send completed swabs to the hospital laboratory for analysis to determine the usability and timeliness of the samples.

Conditions

  • Cardiac Surgery
  • Infection, Soft Tissue
  • Wound Healing
  • Swabs
  • Self Management

Interventions

PROCEDURE

Self-swabbing of surgical wound

Participants will perform self-swabbing of their surgical wound under observation by a research practitioner via secure video call.

Sponsors & Collaborators

  • University of Nottingham

    collaborator OTHER
  • Liverpool Heart and Chest Hospital NHS Foundation Trust

    collaborator OTHER
  • Health Innovation East Midlands

    collaborator UNKNOWN
  • Birmingham Community Healthcare NHS

    collaborator OTHER_GOV
  • University Hospitals Sussex NHS Foundation

    collaborator UNKNOWN
  • Centre for Healthcare Equipment and Technology Adoption

    collaborator UNKNOWN
  • Guy's and St Thomas' NHS Foundation Trust

    lead OTHER

Principal Investigators

  • Sunil Bhudia · Royal Brompton and Harefield Hospitals, part of Guy's and St Thomas' NHS Foundation Trust (GSTFT)

  • Ishtiaq Ahmed · University Hospitals Sussex NHS Foundation Trust

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-06
Primary Completion
2026-02-28
Completion
2026-02-28

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07200401 on ClinicalTrials.gov