Patient Reporting and Action for a Safe Environment (PRASE) intervention: a multi-centred evaluatio

Not Applicable

Completed

• Conditions: Topic: Generic Health Relevance and Cross Cutting Themes; Subtopic: Generic Health Relevance (all Subtopics); Disease: Health Services Research; Not Applicable

• Registration Number: ISRCTN07689702
• Lead Sponsor: Bradford Institute for Health Research (UK)

Brief Summary

2014 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/25354689 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/25862755 2016 results in: http://www.ncbi.nlm.nih.gov/pubmed/27763744 2017 results in: http://www.ncbi.nlm.nih.gov/pubmed/28159854 2018 results in: http://www.ncbi.nlm.nih.gov/pubmed/29545325

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2013-08-16
• Study Completion: 2014-09-30
• Last Update Posted: 30 April 2018

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 2400

Inclusion Criteria

1. Male or female
2. Aged 16 or over, upper age limit 99 years
3. Able to give informed consent
4. Minimum period of two hours on the ward before questionnaire administered
5. Parents or carers of child patients in paediatric wards

Exclusion Criteria

1. Does not have capacity to consent
2. Children under the age of 16
3. Has capacity but is too ill or distressed to take part e.g. breathlessness, pain, bleeding, immediately post-op etc
4. Has taken part in the study within the previous month

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Patient Safety Thermometer data; This is routinely collected ward level data which includes information on:<br>1.1. Pressure ulcers<br>1.2. Venous thromboembolism (VTE)<br>1.3. Catheter associated Urinary Tract Infections<br>1.4. Falls<br>Timepoints: 6 month and 12 months post baseline<br>2. Patient Measure of Organisational Safety (PMOS) questionnaire domain scores<br>Measured at baseline, 6 months, 12 months

Secondary Outcome Measures

Name	Time	Method
1. Three CQUIN questions (from patients, at the end of the questionnaire) measured at baseline, six months, twelve months<br>2. Family & Friends question, which is: ?How likely are you to recommend this ward to friends and family if they needed similar care or treatment?? (from patients, at the beginning of the questionnaire)<br>3. Staff patient safety culture, including:<br>3.1. Questions from national staff survey<br>3.2. Staff satisfaction/morale<br>Measured at baseline, 6 months, 12 months<br><br>The trialists will also seek to access some routinely collected ward-level data from participating wards:<br>1. Patient safety incidents for the study period (as a secondary outcome)<br>2. Staff absence/sickness rates (as a covariate)<br>3. Patient acuity/dependency scores (as a covariate)<br>4. Nurse/patient ratios (as a covariate)<br>Measured at baseline and 12 months