Targeted Letters to Reduce Avoidable Emergency Department Attendances
1 other identifier
interventional
25,000
0 countries
N/A
Brief Summary
The study aims to test whether it is possible to reduce pressure on Emergency Departments by sending a personal feedback letter to people who have recently attended an Emergency Department and whose health issues could likely have been dealt with elsewhere. These attendances clearly have many causes. However, it is likely that some attendances are due to behavioural factors - in other words, the various ways in which users interact with services. This study focuses on one particular behavioural factor: lack of feedback to users making avoidable visits. The study will take place in collaboration with an NHS hospital trust. Each week during the trial, the hospital trust will identify those Emergency Department attendances in the last seven days which, according to clinical judgement, could have been dealt with elsewhere. Patients will then be randomly selected to receive a letter containing information on alternative healthcare options for non-emergency health concerns. Patient records will be analysed to determine whether the patients who received the letter are less likely to make an avoidable repeat visit to the Emergency Department in the future, compared with patients who received no letter.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2015
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedFirst Submitted
Initial submission to the registry
January 6, 2015
CompletedFirst Posted
Study publicly available on registry
January 8, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2015
CompletedJanuary 8, 2015
January 1, 2015
10 months
January 6, 2015
January 7, 2015
Conditions
Outcome Measures
Primary Outcomes (1)
Number of avoidable Emergency Department re-attendances (Attendances are classified as avoidable using the 'No Investigation No Significant Treatment' code.)
Attendances are classified as avoidable using the 'No Investigation No Significant Treatment' code.
Measured at 4 months after previous attendance
Study Arms (2)
Letter
EXPERIMENTALPatients receive a letter containing information on alternative healthcare options for non-emergency health concerns.
No letter
NO INTERVENTIONPatients receive no letter (this is the usual care).
Interventions
Patients receive an information letter following an avoidable visit to the Emergency Department.
Eligibility Criteria
You may qualify if:
- Adults who attended a participating Emergency Department during the trial period and whose attendance was codes as 'No Investigation No Significant Treatment'
You may not qualify if:
- Children under the age of 18
- All departments and hospitals other than participating Emergency Departments.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hannah Behrendt, MPhil, BA
Behavioural Insights Team
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 6, 2015
First Posted
January 8, 2015
Study Start
January 1, 2015
Primary Completion
November 1, 2015
Study Completion
November 1, 2015
Last Updated
January 8, 2015
Record last verified: 2015-01