Longitudinal Observation of NHS Staff Wellbeing Following Introduction of the I-care Peer Support App (I-Care)

November 11, 2022 updated by: University of Southampton

Longitudinal Observation of United Kingdom NHS Staff Wellbeing Following Introduction of the I-care Peer Support App

The coronavirus pandemic has had demonstrable impact upon healthcare workers. For healthcare workers this has meant disruption to vital access to peer support networks. In May 2020 the United Nations (UN) published a policy brief highlighting the importance of supporting mental health and wellbeing for communities affected by coronavirus. There is a need to find innovative solutions to facilitate support in the post-COVID-19 era and some innovations are emerging to fill this void but an evidence, long-term, sustainable, solution is yet to be proposed. In response, a digital app has been co-developed by UK researchers and healthcare staff with the intent to facilitate a virtual peer support mechanism for National Health Service (NHS) staff.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Detailed Description

Rationale: The coronavirus pandemic has had demonstrable impact upon healthcare workers. For healthcare workers this has meant disruption to vital access to peer support networks. In May 2020 the United Nations (UN) published a policy brief highlighting the importance of supporting mental health and wellbeing for communities affected by coronavirus. There is a need to find innovative solutions to facilitate support in the post-COVID-19 era and some innovations are emerging to fill this void but an evidence, long-term, sustainable, solution is yet to be proposed. In response, a digital app has been co-developed by UK researchers and healthcare staff with the intent to facilitate a virtual peer support mechanism for National Health Service (NHS) staff.

Aim: The main aim of this research is to determine the acceptability and efficacy of the newly developed I-care app to facilitate peer-support for NHS staff wellbeing.

Methods: A mixed methods study with concurrent process evaluation will be conducted to explore the acceptability and efficacy of an app-based peer support platform for use by anyone working within Solent NHS Trust with access to an android mobile phone device. Data will be generated from quantitative app usage, binary survey responses, and qualitative interviews.

Populations: All staff within Solent NHS Trust with an android mobile phone will be considered eligible to use the app.

Duration: Data will be collected at one, three, six, and 12-months post app launch.

Expected outcomes: As the innovation developed has spanned biomedical, behavioural and computing science a range of exploratory methods are proposed to establish the reach and uptake of the innovation, early indication of a potential causal model explaining how the innovation could lead to benefit, identification of key components of the innovation as identified by end users, and estimation of overall acceptability and efficacy.

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hampshire
      • Southampton, Hampshire, United Kingdom, SO17 1BJ
        • Lindsey Cherry

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All staff within a single UK Health Trust with an android mobile phone will be considered eligible to use the app.

Description

Inclusion Criteria:

  • All staff within a single UK Health Trust with an android mobile phone will be considered eligible to use the app

Exclusion Criteria:

  • Not employed within the designated Trust
  • Under 18 years of age
  • Unable or unwilling to provide informed consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Wellbeing
Time Frame: 12 months
Most frequent response (A/B/C).
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Engagement
Time Frame: 12 months
Number of participants who have provided a rating
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Lindsey Cherry, PhD, University of Southampton & Solent NHS Trust

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2021

Primary Completion (Actual)

April 1, 2022

Study Completion (Actual)

July 1, 2022

Study Registration Dates

First Submitted

February 2, 2021

First Submitted That Met QC Criteria

March 17, 2021

First Posted (Actual)

March 22, 2021

Study Record Updates

Last Update Posted (Actual)

November 16, 2022

Last Update Submitted That Met QC Criteria

November 11, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 61764

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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