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COVID-19 and Rough Sleepers: A Pilot Randomised Controlled Trial of Models of Housing and Support To Reduce Risks of COVID-19 Infection and Homelessness: Moving On Study, 2020-2022
Creator
Mackie, P, Cardiff University
Cannings-John, R, Cardiff University
Randell, E, Cardiff University
Smallman, K, Cardiff University
Study number / PID
855729 (UKDA)
10.5255/UKDA-SN-855729 (DOI)
Data access
Restricted
Series
Not available
Abstract
This trial outlines a unique time limited opportunity to conduct the first ever randomised controlled trial in the UK, to evaluate the feasibility and acceptability of randomising participants to Settled Accommodation (SA) or Temporary Accommodation (TA) with the aim of preventing COVID-19 infection and reducing housing instability.
The study’s primary objectives were to assess the following:
1. The feasibility of recruiting local authorities and eligible participants to the study.
2. Recruitment rates of participants and retention through 3 months and 6 months post randomisation follow-up data collection.
3. The acceptability of the study and its processes, including randomisation, to single homeless households and local authorities and their willingness to participate in a definitive trial.
In addition, the study also aims to assess the following Secondary objectives:
1. Adherence to the study allocation, reach and fidelity (i.e. whether SA is delivered as intended, works as hypothesized, is scalable and sustainable).
2. The feasibility and acceptability of proposed outcome measures for a definitive trial, including resource use and health-related quality of life data, as methods to measure effectiveness of the intervention and to conduct an embedded health economic evaluation within a definitive RCT.
3. The feasibility and acceptability of linkage to routinely collected data within a definitive RCT by assessing whether (a) participants are willing to consent for their data to be linked and (b) personal identifiers can be linked to NHS Digital routine datasets.
Quantitative data was collected at baseline and follow-up at 3 and 6 months. 50 participants were invited to complete outcome measures. These participants completed the questionnaire over the telephone with trained members of staff based at the University. Data was entered into Qualtrics application system and used to collect consent and questionnaire response data. The trial explored past and...
Terminology used is generally based on DDI controlled vocabularies: Time Method, Analysis Unit, Sampling Procedure and Mode of Collection, available at CESSDA Vocabulary Service.
Methodology
Data collection period
06/08/2020 - 30/03/2022
Country
United Kingdom
Time dimension
Not available
Analysis unit
Individual
Universe
Not available
Sampling procedure
Not available
Kind of data
Numeric
Text
Data collection mode
50 participants were recruited through two Local Authorities. Eligibility to participate will be limited to rough sleepers and in single-person households, aged 18 and over. Participants provided informed consent and were enrolled in the trial for at least 6 months, from baseline up to and including the 6 month follow up. All baseline and follow up data collection were completed remotely via telephone interview. Qualitative interviews with 14 participants who consented to speak to the research team were conducted over the telephone. Interviews focussed on their experience of taking part in the trial. One of the Moving On researchers also took part in an interview to describe their experiences of trial procedures.
Funding information
Grant number
ES/V011855/1
Access
Publisher
UK Data Service
Publication year
2022
Terms of data access
The Data Collection is available for download to users registered with the UK Data Service.