Work And Vocational advicE Study - Effectiveness of Adding a Brief Vocational Support Intervention to Usual Primary Care (WAVE)
Primary Purpose
Musculoskeletal Pain, Mental Health Issue, Mental Health Disorder
Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Vocational Support
Sponsored by
About this trial
This is an interventional supportive care trial for Musculoskeletal Pain focused on measuring Work absence, Other health conditions, Return to work, Musculoskeletal pain, Mental health
Eligibility Criteria
Inclusion Criteria:
- Adults aged 18 years and over
- currently in paid employment (full or part time)
- current absence from work of at least two consecutive calendar weeks but not more than six continuous months
- received a fit note
- access to a mobile phone that can receive and respond to SMS text messages
- able to read and write English
- able to give full informed consent
- willing to participate.
Exclusion Criteria:
- Long-term work absence defined as over six continuous months
- pregnancy or on maternity leave
- patients presenting with signs or symptoms indicative of serious illness requiring urgent medical attention ('red' flags)
- severe mental health problems (e.g. severe depression with risk of self-harm, exacerbation of schizophrenia or bipolar disorder, cognitive impairment or lack of capacity)
- high vulnerability (e.g. palliative stages of illness, recent bereavement, dementia).
Sites / Locations
- Keele University
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Usual care
Usual care plus vocational support
Arm Description
Participants randomised to the usual care arm will continue to receive care as usual for their health and vocational needs. For most patients, this will comprise usual clinical care, without formal vocational advice.
Vocational support following a stepped care model based on the principles of case management in addition to usual primary care.
Outcomes
Primary Outcome Measures
Number of days absent from work
Self reported work absence calculated as the number of days off work over the previous 6 months (since randomisation).
Secondary Outcome Measures
Return to work
RTW - Self reported number of days until return to work over 6 months, or until a sustained return to work is achieved (defined as return to any work for 4 consecutive weeks).
Work interference
Work Productivity Activity Impairment (WPAI) Questionnaire to measure impairments to work and activities in the past seven days. The WPAI provides four sets of scores; absenteeism, presenteeism, work productivity loss and activity impairment. Scores are multiplied by 100 to express percentages with higher numbers indicating greater impairment and less productivity i.e. worse outcomes.
Work performance
Single Item Productivity Questionnaire (SIPQ) measured using a Visual Analogue Scale with scores ranging from 0 (health has not impacted on work performance at all) to 10 (health is so bad participant has been unable to do their job) a higher score indicates a worse outcome. The scores will be reported as a percentage perceived loss in productivity.
Full Information
NCT ID
NCT04543097
First Posted
August 12, 2020
Last Updated
October 17, 2023
Sponsor
Keele University
Collaborators
University of Southampton, Guy's and St Thomas' NHS Foundation Trust, University of Birmingham, Aston University
1. Study Identification
Unique Protocol Identification Number
NCT04543097
Brief Title
Work And Vocational advicE Study - Effectiveness of Adding a Brief Vocational Support Intervention to Usual Primary Care
Acronym
WAVE
Official Title
Work And Vocational advicE (WAVE) in Primary Care: a Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 23, 2020 (Actual)
Primary Completion Date
April 20, 2023 (Actual)
Study Completion Date
November 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Keele University
Collaborators
University of Southampton, Guy's and St Thomas' NHS Foundation Trust, University of Birmingham, Aston University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Maintaining the population's fitness for work is a priority for the UK Government. People with poor health often struggle at work and take sick leave. Work brings financial, social and health benefits. Few employees receive support to manage their health at work, known as vocational advice, so when their health affects work they visit their general practitioner (GP). The investigators have recently shown the benefits of providing vocational advice for adults consulting in primary care with musculoskeletal pain.
The WAVE study research question is: in patients consulting in general practice who receive a fit note for time off work, does a brief vocational advice intervention lead to fewer days lost from work than usual primary care, and is it cost-effective?
WAVE includes a feasibility phase to adapt a vocational advice intervention for a broader group of patients and test it in a small sample of patients; followed by a pragmatic, multi-centre, two-arm, parallel-group randomised (1:1) trial with internal pilot phase, mixed methods process evaluation and health economic analysis.
Patients will be randomised to either (i) vocational advice intervention plus usual care, or (ii) usual care alone. The vocational advice intervention is designed as a stepped care model based on the principles of case management and delivered by trained Vocational Support Workers (VSWs).
The investigators will also interview patients, General Practitioners (GPs), VSWs and employers to understand their views about the intervention and return to work.
Participants in the trial will be followed-up over 6 months with fortnightly text messages and postal questionnaires at 6 weeks and 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Musculoskeletal Pain, Mental Health Issue, Mental Health Disorder, Other Physical Health Condition, Absence
Keywords
Work absence, Other health conditions, Return to work, Musculoskeletal pain, Mental health
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Participants, their treating clinicians and VSWs cannot be blinded to allocation due to the nature of the intervention. The data will be analysed independently by two statisticians one of whom will be blinded to intervention allocation the other statistician will be unblinded to allow intervention delivery details to be reported to the Trial Steering Committee (TSC) / Data Monitoring Committee (DMC) if required.
Allocation
Randomized
Enrollment
130 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Participants randomised to the usual care arm will continue to receive care as usual for their health and vocational needs. For most patients, this will comprise usual clinical care, without formal vocational advice.
Arm Title
Usual care plus vocational support
Arm Type
Experimental
Arm Description
Vocational support following a stepped care model based on the principles of case management in addition to usual primary care.
Intervention Type
Behavioral
Intervention Name(s)
Vocational Support
Intervention Description
Participants randomised to receive vocational advice will all be offered:
Step 1, contact by phone to undertake an assessment with a trained Vocational Support Worker (VSW) to identify obstacles to Return to Work (RTW) and support RTW planning.
Step 2, face-to-face (in person or by videoconference) in-depth discussion of obstacles to RTW and further support for RTW planning.
Step 3, contact by the VSW (with participant consent) with the participants' workplace.
The frequency of contact will be individualised to the needs of participants and the offer of support continued until sustained RTW (defined as return to any work for at least 4 weeks) or until 6 months of absence, after which participants will be signposted to other services.
Primary Outcome Measure Information:
Title
Number of days absent from work
Description
Self reported work absence calculated as the number of days off work over the previous 6 months (since randomisation).
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Return to work
Description
RTW - Self reported number of days until return to work over 6 months, or until a sustained return to work is achieved (defined as return to any work for 4 consecutive weeks).
Time Frame
6 months or until sustained return to work (return to any work for 4 consecutive weeks)
Title
Work interference
Description
Work Productivity Activity Impairment (WPAI) Questionnaire to measure impairments to work and activities in the past seven days. The WPAI provides four sets of scores; absenteeism, presenteeism, work productivity loss and activity impairment. Scores are multiplied by 100 to express percentages with higher numbers indicating greater impairment and less productivity i.e. worse outcomes.
Time Frame
6 months
Title
Work performance
Description
Single Item Productivity Questionnaire (SIPQ) measured using a Visual Analogue Scale with scores ranging from 0 (health has not impacted on work performance at all) to 10 (health is so bad participant has been unable to do their job) a higher score indicates a worse outcome. The scores will be reported as a percentage perceived loss in productivity.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults aged 18 years and over
currently in paid employment (full or part time)
current absence from work of at least two consecutive calendar weeks but not more than six continuous months
received a fit note
access to a mobile phone that can receive and respond to SMS text messages
able to read and write English
able to give full informed consent
willing to participate.
Exclusion Criteria:
Long-term work absence defined as over six continuous months
pregnancy or on maternity leave
patients presenting with signs or symptoms indicative of serious illness requiring urgent medical attention ('red' flags)
severe mental health problems (e.g. severe depression with risk of self-harm, exacerbation of schizophrenia or bipolar disorder, cognitive impairment or lack of capacity)
high vulnerability (e.g. palliative stages of illness, recent bereavement, dementia).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gwenllian Wynne-Jones, PhD
Organizational Affiliation
Keele University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Keele University
City
Newcastle Under Lyme
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Any requests for access to the data from anyone outside of the research team (e.g. collaboration, joint publication, data sharing requests from publishers) will follow the Keele University's data sharing procedure.
Learn more about this trial
Work And Vocational advicE Study - Effectiveness of Adding a Brief Vocational Support Intervention to Usual Primary Care
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