Redesigning Pre-surgery Patient Journeys With Telehealth

Sponsor
KK Women's and Children's Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05781789
Collaborator
Duke-NUS Graduate Medical School (Other), Nanyang Technological University (Other)
258
1
37.9
6.8

Study Details

Study Description

Brief Summary

Prior to surgery, patients undergo preanaesthesia assessment to ensure timely optimisation of medical conditions that could adversely impact perioperative outcomes. At the Preadmission Service (PAS) clinic of KK hospital, nurses perform the first triage to identify patients who require outpatient anaesthetic review in advance of surgery. While all elective patients attend the PAS clinic, only 8% are require outpatient anaesthetic review. The majority 92%, can be safely triaged to receive preanaesthesia assessment on the day of surgery. In this project, we propose to investigate the efficacy of a new pre-surgery workflow for elective surgical patients incorporating telehealth. We hypothesize that the redesigned pre-surgery journey incorporating telehealth reduces in-person consultation at the pre-admission clinic by up to 90%. Primary outcome is the proportion of eligible same-day-admission patients assessed via telehealth. Secondary outcomes are:

  1. Patient cost and time savings

  2. Patient experience of the new model of care

  3. Staff experience of the new workflow

  4. Incidence of day-of-surgery cancellations

Condition or Disease Intervention/Treatment Phase
  • Other: Telehealth for preoperative evaluation

Detailed Description

Prior to elective surgery, patients undergo preanaesthesia assessment to ensure timely optimisation of medical conditions that could adversely impact perioperative outcomes. Preadmission Service (PAS) clinic nurses at KK Hospital perform pre-surgery triage to identify patients requiring outpatient anaesthetic review. PAS data shows that only 8% of same-day-admission (SDA) patients needed an anaesthetist's review; the majority (92%) can be safely triaged to receive preanaesthesia assessment on the day of surgery. The aim of this study is to investigate the service re-design, efficacy and effectiveness of a new telehealth pre-surgery model of care for elective SDA patients. We hypothesize that the telehealth pre-surgery new model of care will achieve an expected 50% uptake for SDA patients as the primary outcome during implementation. Secondary outcomes are patient cost savings, patient experience of the new model of care, and staff experience ofthe new workflow. We will use a sequential exploratory mixed methods study design, consistent with the 5-stage model for telehealth research. An implementation science framework - the Normalisation Process Theory, underpins our 3-phase study. Phase 1 (service redesign) explores the feasibility of presrugery telehealth via semi-structured interviews of patients and healthcare staff. Phase 2 (preimplementation) investigates efficacy of the telehealth model of care by addressing service fidelity, and patient and staff experience using administrative data. Phase 3 is a pragmatic trial to ascertain effectiveness of the telehealthmodel of care, addressing the primary and secondary outcomes stated. This novel study using implementation science to redesign and implement presurgery telehealth will inform scale-up, spread, and sustainability of a new model of care within SingHealth and other health clusters in Singapore.

Study Design

Study Type:
Observational
Anticipated Enrollment :
258 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Redesigning Pre-surgery Patient Journeys With Telehealth
Actual Study Start Date :
Oct 3, 2022
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Patient participants

Patient booked for elective surgery and: Age 21 to 70 years English literacy Willing to provide signed consent Of any nationality Able to give own legal consent

Other: Telehealth for preoperative evaluation
Conduct of preoperative evaluation remotely using Zoom application
Other Names:
  • Video consultation
  • Healthcare provider participants

    Criteria: Age 21 to 70 years Healthcare professionals comprising clinic staff (surgical outpatient clinics, PAS), clinicians (anaesthetists, surgeons), and health service managers) working in the perioperative clinical areas

    Other: Telehealth for preoperative evaluation
    Conduct of preoperative evaluation remotely using Zoom application
    Other Names:
  • Video consultation
  • Outcome Measures

    Primary Outcome Measures

    1. Proportion of eligible elective surgery patients assessed successfully via telehealth for preoperative evaluation [One year from the initiation of the implementation phase (Phase 3)]

      Of the total number of patients booked for elective surgery, the proportion of patients evaluated preoperatively by telehealth is measured.

    Secondary Outcome Measures

    1. Patient's perception and attitude towards a Telehealth model of care for preoperative evaluation [5 months from July to November 2021]

      Quantitative study via one-on-one semi-structured interviews of elective surgery patients to evaluate their attitudes and perception of the new proposed telehealth workflow conducted in (Service Redesign) Phase 1

    2. Healthcare providers' perception and attitude towards a Telehealth model of care for preoperative evaluation [5 months from July to November 2021]

      Quantitative study via one-on-one semi-structured interviews of healthcare providers working in the peroperative and surgery clinics to evaluate their attitudes and perception of the new proposed telehealth workflow conducted in (Service Redesign) Phase 1

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient participants:

    Age 21 to 70 years Listed for elective surgery English literacy Willing to provide signed consent Of any nationality Able to give own legal consent

    Exclusion Criteria:
    • Healthcare participants:

    Age 21 to 70 years Healthcare professionals comprising clinic staff (surgical outpatient clinics, PAS), clinicians (anaesthetists, surgeons), and health service managers)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 KK Women's and Children's Hospital Singapore Singapore 229899

    Sponsors and Collaborators

    • KK Women's and Children's Hospital
    • Duke-NUS Graduate Medical School
    • Nanyang Technological University

    Investigators

    • Study Chair: Chai-Rick Soh, FANZCA, Singapore General Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    KK Women's and Children's Hospital
    ClinicalTrials.gov Identifier:
    NCT05781789
    Other Study ID Numbers:
    • AM/HRT/008/2021
    First Posted:
    Mar 23, 2023
    Last Update Posted:
    Mar 23, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by KK Women's and Children's Hospital

    Study Results

    No Results Posted as of Mar 23, 2023