Study Stopped
Early data showed an improvement in length of stay and patient satisfaction, but the nursing time that had been provided for free was subsequently withdrawn, and it was necessary to stop the trial before sufficient data had been collected.
Neurosurgical Transitional Care Programme
TCP
Transitional Care Services: A Quality and Safety Process Improvement Programme in Neurosurgery
2 other identifiers
interventional
242
1 country
1
Brief Summary
Readmissions increasingly serve as a metric of hospital performance, inviting quality improvement initiatives in both medicine and surgery. Recently, a readmission reduction program in the United States was associated with significantly shorter length of stay, earlier discharge, and reduced 30-day readmission after elective neurosurgery. These results underscore the importance of patient education and surveillance after hospital discharge, and it would be beneficial to test whether the same approach yields beneficial results in a different health system, the NHS. In this study, the investigators will replicate the Transitional Care Program (TCP) with the goal of decreasing length of stay, improving discharge efficiency, and reducing readmissions in neurosurgical patients by optimizing patient education and post-discharge surveillance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable surgery
Started May 2019
Shorter than P25 for not_applicable surgery
1 active site
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
June 5, 2018
CompletedFirst Posted
Study publicly available on registry
July 20, 2018
CompletedStudy Start
First participant enrolled
May 30, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 18, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2019
CompletedMay 2, 2025
April 1, 2025
3 months
June 5, 2018
April 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Length of Hospital Stay
Time from admission until discharge (reported in hours)
From time of hospital admission until the time of first hospital discharge or time of death from any cause, whichever came first. Assessed up to 4 months post-admission.
Secondary Outcomes (4)
Hospital Readmission
From the time of hospital discharge from the original admission until 30 days after hospital discharge
Discharge before 12:00pm
This is assessed on the date of discharge from time 00:00 to time 23:59. The actual time of discharge or time of death from any cause, whichever came first, will be noted. Assessed up to 4 months post-admission.
Cost
The cost of the hospital admission will be calculated for the time frame from the initial hospital admission until 30 days after hospital discharge, or time of death from any cause.
Patient Satisfaction scores based on a single survey provided to the patient at the time of discharge.
From the time of hospital discharge from the original admission up until 2 weeks after discharge
Study Arms (2)
Transitional Care Programme
EXPERIMENTALThe primary intervention of the Transitional Care Programme (TCP) will be additional patient education, framing of expectations for the hospital course and length of stay, coordinated team preparation for discharge, a dedicated discharge appointment, and a follow up phone call.
Standard of Care
NO INTERVENTIONPatients are admitted without a pre-determined discharge date. They do not receive a dedicated discharge appointment, and will not receive a follow up phone call 48 hours after discharge.
Interventions
These patients will receive a pre-admission overview of their surgery, an anticipated discharge date, and a pre-scheduled discharge appointment to set patient expectations for a shorter hospitalization. On the day of discharge, the patient and his or her caregiver will attend an extended discharge appointment with a TCP-trained nurse. Finally, patients will receive a surveillance phone call 48 hours after discharge.
Eligibility Criteria
You may qualify if:
- Patients are eligible for the TCP if scheduled for elective neurological surgery (including spinal surgery performed by an orthopedic surgeon) and were expected to have a discharge disposition to home.
You may not qualify if:
- Patients with an anticipated discharge to a facility other than home
- Patients with an anticipated discharge to home who are then discharged to a facility other than home will be excluded from the statistical analysis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Barts & The London NHS Trustlead
- Brigham and Women's Hospitalcollaborator
- Harvard Medical School (HMS and HSDM)collaborator
Study Sites (1)
Bart's Health NHS Trust
London, United Kingdom
Related Publications (3)
Robertson FC, Logsdon JL, Dasenbrock HH, Yan SC, Raftery SM, Smith TR, Gormley WB. Transitional care services: a quality and safety process improvement program in neurosurgery. J Neurosurg. 2018 May;128(5):1570-1577. doi: 10.3171/2017.2.JNS161770. Epub 2017 Jul 14.
PMID: 28707992BACKGROUNDJones CE, Hollis RH, Wahl TS, Oriel BS, Itani KM, Morris MS, Hawn MT. Transitional care interventions and hospital readmissions in surgical populations: a systematic review. Am J Surg. 2016 Aug;212(2):327-35. doi: 10.1016/j.amjsurg.2016.04.004. Epub 2016 Jun 1.
PMID: 27353404BACKGROUNDVerhaegh KJ, MacNeil-Vroomen JL, Eslami S, Geerlings SE, de Rooij SE, Buurman BM. Transitional care interventions prevent hospital readmissions for adults with chronic illnesses. Health Aff (Millwood). 2014 Sep;33(9):1531-9. doi: 10.1377/hlthaff.2014.0160.
PMID: 25201657BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Edward McKintosh, FRCS(SN) PhD
Barts Health
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- All eligible patients will be consented to participate in the study. If they consent, a non-clinician study team member will randomise the patient into the control or intervention arm. Thereafter, all members of the care team will be notified of the patient's allocation in order to deliver the TCP.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 5, 2018
First Posted
July 20, 2018
Study Start
May 30, 2019
Primary Completion
August 18, 2019
Study Completion
August 30, 2019
Last Updated
May 2, 2025
Record last verified: 2025-04