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CompletedNCT03269487PERFECTEDUpdated Aug 31, 2017

PERFECTED WP2: Implementing Optimised Hospital Care

An observational study in Implementation of Enhanced Recovery Pathway, sponsored by University of East Anglia. Completed. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-08-31.

Sponsored by University of East Anglia · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
270
Ages
18 Years and older
Sex
All
01

Study summary

This study is part of the 5-year long (2013-18) PERFECTED (Peri-operative Enhanced Recovery hip-fracture Care of paTiEnts with Dementia) National Institute for Health Research (NIHR) funded research programme.

PERFECTED's aim is to develop and pilot an evidence-based intervention to improve the hospital care of patients living with dementia who have fractured their hip. This protocol relates to Work Package 2 (WP2) of PERFECTED only.

By working collaboratively with local clinicians and stakeholders, an action research (plan-do-study-act) approach will be used to generate knowledge to understand how to best implement the intervention (PERFECTED Enhanced Recovery Pathway), which was developed from learning and research undertaken as part of Work Package 1. During the current study the PERFECTED Enhanced Recovery Pathway (ERP) will be used to optimise care on three ortho-geriatric wards for 12 months. These wards are located in Norfolk, Nottinghamshire and Yorkshire. The sole participants are NHS personnel delivering care on selected wards.

Data collection activities (observations, in-field interviews, documentary analysis and quantitative data generated from the PERFECTED ERP implementation checklist) will determine the staff training and cultural changes required to implement and maximise adherence to the PERFECTED ERP. Simultaneously, enabling the identification and exploration of areas of optimised, satisfactory and sub-optimal care. By working in partnership within and across the partner wards, action plans to address sub-optimal care will be generated, implemented and reviewed. Findings will inform the best ways to optimise care via the implementation of the PERFECTED ERP. Knowledge generated during this study will be used to develop an ERP and staff training manual. This will aid implementation of the intervention arm of a latter Cluster Randomised Control Trial (Work Package 3), ensuring the PERFECTED ERP can be utilised in the real world.

As part of PERFECTED's commitment to Public Patient Involvement (PPI), lay researchers will be trained to assist with qualitative research activities.

02

Conditions studied

  • Implementation of Enhanced Recovery Pathway
03

In context

Lead sponsor

University of East Anglia is the lead sponsor of 79 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Sole participant group for this study are NHS employees involved in care delivery on partner hospital wards.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • NHS employee or student nurse
  • Involved in the delivery of care to patients on partner wards in which the PERFECTED ERP is being implemented

Exclusion criteria

Exclusion Criteria:

* None

05

Study design

Observational model
Other
Time perspective
Other
Enrollment
270 participants (actual)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • Healthcare professionals in partner sites

    NHS employee or student nurse involved in the delivery of care to patients on partner wards in which the PERFECTED ERP is being implemented.

06

What researchers measure

Primary outcomes

  1. PERFECT-ER

    Improvement toolkit

    Time frame: 12 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03269487
Lead sponsor
University of East Anglia
Responsible party
Sponsor
First posted
Aug 31, 2017
Start date
Aug 1, 2015
Primary completion
Jul 1, 2016
Completion
Sep 1, 2016
Last update
Aug 31, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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