jro-study-summary.md

description	Simple summary as per UCLH JRO interventional studies protocol

JRO study summary

IRAS Number
REC Reference No.
Sponsor Reference No.
Other research reference number(s) (if applicable)	(e.g. UCL Data Protection number)
Full (Scientific) title	INGLES-Guidelines In‑situ Nudges for Guidelines, Local resistance, Estimated Susceptibility
Health condition(s) or problem(s) studied	Antibiotic guideline compliance via electronic point-of-care alerts
Study Type i.e. Cohort etc	Randomised Controlled Trial
Aim(s):	Improve guideline compliance for antibiotic prescribing through targeted notifications at the point of care
Objectives:	Primary To improve compliance with hospital antibiotic prescribing guidelines Secondary To reduce prescribing of 'watch' or 'reserve' antibiotics To reduce the antibiotic spectrum of antibiotics given To increase the switch to oral antibiotics To reduce complications associated with antibiotic prescribing (resistance, diarrhoea etc.)
Type of trial:	Single centre, parallel assignment, randomised controlled trial without masking
Trial design and methods:	PICO
Trial duration per participant:	7 days
Key Study milestones	Approved peer review of protocol JRO submission and sponsorship HRA and NHS REC approval 1st patient recruited
Estimated total trial duration:	TODO
Planned trial sites:	University College Hospital London
Total number of participants planned:	TODO
Main inclusion/exclusion criteria:	Patients presenting to UCLH with a new community acquired pneumonia
Statistical methodology and analysis:	Briefly describe the statistical methodology to be used in the trial.
FUNDING & OTHER
Funding	UCLH Biomedical Research Centre
Other support	Insert details of the non-financial support given, and the names & contact details of all organisation providing the non-financial support.
STORAGE of SAMPLES / DATA (if applicable)
Human tissue samples	N/A
Data collected / Storage	TODO
KEY STUDY CONTACTS Full contact details including phone, email and fax numbers	TODO
Committees	TODO Name(s) of committees, full contact details including, phone and email. E.g. study steering groups. For each committee/group, the protocol should state their roles and responsibilities and degree of independence from the Sponsor and Investigators.
Sub-contractors	None
Other relevant study personnel	TODO (E.g. Data Custodian and Data Processors)

{% hint style="info" %} See UCL/UCLH Interventional studies protocol template {% endhint %}