IPS-AD is a pragmatic, multi-centre, two-arm, parallel group, superiority RCT, with a realist process evaluation. The aim of the study is to determine the effectiveness of IPS to help people with AUD, OUD and other drug use disorders obtain employment in the open competitive job market. These questions will be answered by pre-registered analyses of primary and secondary outcomes recorded across an 18-month follow-up after randomisation (Figure 1). There are also planned analyses of outcome mediation and effectiveness over the longer term.
After enrolment, all study participants will continue to be enrolled in addiction treatment (co-ordinated by a clinician called a keyworker) and may receive standard employment support (conventionally termed treatment-as-usual [TAU] – the control condition), or they will continue to be enrolled in addiction treatment, and may receive standard employment support, and enrolled in IPS – the intervention condition.
The study will be reported following the CONSORT guideline (Consolidated Standards of Reporting Trials; http://www.consort-statement.org/) extension for non-medication trials  and the Template for Intervention Description and Replication (TIDieR) checklist for reporting interventions . This protocol has been written following the SPIRIT checklist for intervention trials  – see Supplementary Material (Table S1).
IPS-AD will be conducted following the principles of the Declaration of Helsinki , the Medical Research Council Guidelines for Good Clinical Practice , and the NHS Research Governance Framework . Participants will have the right to withdraw from the trial at any time without giving a reason. There is no anticipated harm and compensation arising from trial participation.
Study population and setting
Study populations will be adults, unemployed and economically inactive , enrolled in community treatment for AUD, OUD or another drug use disorder. The minimum total target sample will be 832 participants. The plan is to include seven clinical recruitment sites in Birmingham, Blackpool, Brighton and Hove, Derbyshire, London Borough of Haringey, Sheffield and Staffordshire. Each site will be a NHS, not-for-profit, or private organisation providing community/outpatient treatment for alcohol and drug dependence. According to the treatment capacity of each site, two or more Employment Specialists (ES) will deliver IPS.
Participant inclusion criteria
Patients will be eligible to take part if they meet the following inclusion criteria:
- Aged 18-65 years
- Enrolled in treatment for drug or alcohol use disorder for at least 14 days with current diagnosis of a specified drug and/or alcohol use disorder
- Unemployed or inactive at study screening visit for at least 6 months with declared wish to obtain open job market employment
- Able to attend the community addiction clinic as required in the protocol
- Able to communicate (verbal and written English) at a level required to engage with a psychosocial intervention
- Able to provide personal National Insurance Number (NINO) to facilitate data linkage .
Participant exclusion criteria
Otherwise eligible patients will not be able to join the study if one or more of the following exclusion criteria are met:
- Currently receiving detoxification treatment for drug or alcohol withdrawal
- Clinically significant (or otherwise uncontrolled) severe mental health, intellectual disability, organic brain disease or dementia, or physical disability that is judged by the local clinical lead to prevent the person accepting IPS
- Suicide planning (past month) or suicide attempt (past 6 months)
- Current legal proceedings which are likely to result in imprisonment
- Enrolment in an IPS trial, or in the past 6 months
- Previously enrolled in the IPS-AD study.
All keyworkers and ES will complete National Institute for Health Research’s Good Clinical Practice (GCP) training. Potential participants will be referred to an ES in the clinical team to discuss the study. The King’s College London Clinical Trials Unit will programme and independently manage the study randomisation system on a secure website. Immediately after securing informed consent (IPS-AD participant information sheet and participant consent form is available from the corresponding author on request) and completion of baseline study questionnaires, the ES will access the randomisation website to assign the participant to the intervention or control condition. Group allocation (ratio 1:1) will be done using block randomisation (with varying block size) stratified by site, clinical diagnosis (AUD, OUD, other drug use disorder), and work history (1 month or less versus more than 1 month of paid employment in last five years).
The randomisation system will immediately confirm the participant’s allocation to IPS or TAU by email. The ES will then inform the participant and their keyworker. Participants assigned to TAU will be given an information pack containing details of standard employment support services available locally and will have no further contact with the ES. It will not be feasible to blind clinicians to trial condition allocation. Enrolment in TAU will be ongoing after the trial according to patient preference and local policy.
IPS intervention principles and delivery
IPS will be offered as an individual (one-to-one) intervention for 9 months with up to 4 additional months of in-work support if competitive employment is attained. IPS will be provided without restriction due to job readiness, work history, qualifications, and homelessness. In weekly sessions in the first month, the ES will: (1) discuss opportunities to work and will give advice on welfare benefits, including the availability of in-work benefits; (2) develop a vocational profile of the participant’s skills, experience and employment preferences; (3) help the participant write or update their curriculum vitae/resume; and (4) help the participant implement a rapid job search. As appropriate, the ES will contact local employers and help the participant complete job applications and prepare for interviews. The ES will seek to develop relationships with local employers and discuss opportunities to tailor work for people recovering from alcohol and drug dependence.
After the first month, IPS sessions will be scheduled approximately fortnightly, with additional phone and email contact provided as needed. Once the participant starts work, the ES will offer in-work support. This support will be approximately weekly contacts in the first month, then fortnightly. The ES will discuss how the participant is adapting to new job; assist with any referral for medical treatment; and, with consent, seek to discuss job flexibility issues with the employer (e.g. adjusting shift patterns to enable the participant to collect treatment medication from a retail pharmacy).
Standard employment support
Vocationally, participants randomised to the TAU control group will receive standard employment support only. For participants receiving Jobseeker’s Allowance (JSA) or Universal Credit (UC) with all work-related requirements, TAU will usually involve support from Jobcentre Plus (JCP) and/or the Work and Health Programme (WHP). TAU may also include standard employment support provided by the addiction treatment programme or other local services .
IPS training for ES
Training for ES will consist of a continuing professional development (CPD) accredited two-day course facilitated by the Centre for Mental Health (CMH) and a 12-week online ES practitioner skills course provided by the USA IPS Employment Center. IPS-AD recruitment sites will be encouraged to look for CPD opportunities for the ES team, including forging links with the local IPS Centre of Excellence and with IPS Grow (the latter an IPS capacity building network in the NHS and mental health services with support funding from NHS England and the DWP).
To help develop and maintain IPS fidelity, IPS-AD will use the 25-item Individual Placement and Support Fidelity Scale (IPS-25) . The IPS-25 was adapted to the UK context by the CMH  and has three sections: staffing, organization and services. Independent reviewers score items on the scale using a 5-point response format (1 = no implementation; 5 = full implementation), with intermediate numbers representing progressively greater degrees of implementation. The maximum score is 125 points. During the study, the CMH will coordinate all fidelity reviewers with another organisation called Social Finance (SF). CMH and SF raters will complete the IPS-25 with access to multiple sources of information, including interviews with study participants, ES and managers, as well as reviewing case records and observing the day-to-day practice of the IPS and clinical teams. From the start of the study, there will be planned fidelity reviews at each site at 5-7 months and 15-18 months. CMH and SF will provide each site with a detailed report of their IPS-25 score and will provide advice on how this can be improved.
Realist process evaluation
RAND Europe and the CMH will conduct the IPS-AD process evaluation. Theory-driven and following realist principles, this will investigate IPS and clinical practice and answer questions of the characteristics of patients and IPS exposure that are associated with competitive employment outcomes. An initial focus will be on any obstacles encountered during the set-up of IPS in each site and how IPS is integrated into routine procedures. In each site, RAND Europe and CMH researchers will conduct personal interviews (each audio recorded with permission) with a random sample of participants allocated to IPS and TAU as well as a convenience sample of ES, treatment service commissioners, managers, keyworkers, local JCP staff and employers.
Primary outcome measure
The primary outcome of the study is competitive employment status. This outcome will be met if the participant obtains at least 7 hours (i.e. one day) of employment in the open competitive job market at any time following randomisation to the end of an 18-month follow-up. This outcome measure has been commonly used in IPS efficacy studies and meta-analysis. We will determine this outcome by linking participant-level information with the Department for Work and Pensions’ (DWP) Work and Pensions Longitudinal Study (WPLS) database.
Secondary outcome measures
IPS-AD includes the following secondary vocational outcome measures:
- Total time (days) in competitive employment (and corresponding National Insurance contributions [NIC] and tax paid)
- Time (days) from randomisation to first competitive employment
- Number of competitive job appointments
- Job tenure (length of longest held competitive employment)
- Sustained employment (tenure in a single appointment for at least 13 weeks)
- Job search self-efficacy
The time and count-based vocational outcomes will be determined from extracts of the WPLS database using the dates of starting and stopping competitive employment. NIC and tax records from randomisation to the end of follow-up will be determined using HMRC’s Real Time Information system (RTI).
Job search self-efficacy (for a mediation analysis of outcome) will be assessed by the 6-item Job Search Self-Efficacy Scale-Behaviour scale (JSSE-B) . The JSSE-B includes measures of confidence in making a good impression, making a good application, and using friends and contacts to discover vacancies. The JSSE-B has been shown to predict job search behaviour. Site clinicians will complete the JSSE-B during personal interviews at baseline, 6 months, 12 months, and 18 months or at treatment exit if earlier (the latter if feasible).
Alcohol and drug dependence treatment-related
For the secondary outcomes and economic analyses, the following alcohol and drug dependence treatment-related outcomes will be included:
- Alcohol consumption, drug use, drug injecting
- DSM-5 AUD, OUD and other drug use disorder remission status
- Total time enrolled in alcohol and drug use disorder treatment
- Number of AUD, OUD and other drug use disorder treatment episodes
- Treatment status at end of follow-up (enrolled, left successfully, left unsuccessfully, deceased)
Alcohol and drug use (recall: past 28-days) will be self-reported to site clinicians using the Treatment Outcomes Profile (TOP) . The TOP is the English national outcomes monitoring instrument for publicly funded treatment services for drug and alcohol dependence. TOP data is uploaded to the National Drug Treatment Monitoring System (NDTMS). The TOP uses a structured, calendar-prompt, ‘timeline follow-back’ procedure  to maximise accuracy of drug and alcohol use reporting. The TOP will be administered by site clinicians as a structured personal interview at baseline, 6 months, 12 months,18 months and exit.
DSM-5 remission status will be assessed by personal interview by site clinicians at baseline, 6 months, 12 months and 18 months using the Structured Clinical Interview for DSM-5 (clinician version; SCID-5-CV) . This has a checklist of 11 symptoms (each coded ‘present ’or ‘absent’) to diagnose disorder presence and severity (no symptoms = disorder not present; 1-3 symptoms = mild; 4-5 symptoms = moderate; ≥6 symptoms = severe). We will use the American Psychiatric Association's definition for AUD and OUD remission (i.e. zero criteria except craving and using the 'on maintenance therapy' specifier as appropriate and not including tolerance and withdrawal item if the patient is adherent to their prescription).
NDTMS records will be used to determine each participant's total time in treatment in the community and in prison, as well as the number of treatment episodes and status at the end of follow-up. For data modelling, we will record TOP and treatment exposure data for 18-months prior to randomisation for those members of the cohort with a history of prior treatment for alcohol and drug dependence.
Social and health
For the economic analysis, the following social and economic outcomes will be included:
- Welfare payments (i.e. Job Seeker’s Allowance [JSA]; Income Support [IS] Employment and Support Allowance [ESA]; Universal Credit [UC]; Housing Benefit [HB] and Tax Credits [TC])
- NHS hospital attendances and admissions (A&E, outpatient and inpatient)
- Prison sentences
JSA, IS, ESA, UC and HB welfare payments will be determined from the dates of starting and stopping receipt of each benefit type, or changes to levels of payment of each type, recorded in the following DWP databases: National Benefits Database (JSA, IS and ESA); and Universal Credit Official Statistics (UC), Housing Benefit Extract (HB). Tax Credit spells and amounts will be determined by use of HMRC’s General Matching System (GMS).
Hospital care will be recorded by Hospital Episode Statistics (HES; PHE is the data controller). The Office for National Statistics' (ONS) register of births and deaths will record mortality.
Convictions and prison sentences will be recorded from extracts from the Police National Computer (PNC) and the National Offender Management Information System (p-NOMIS), respectively (both operated by the Ministry of Justice).
The EQ-5D-5L  is a brief generic scale recording mobility, self-care, usual activities, pain/discomfort, anxiety/depression, with a 0 to 100-point vertical visual analogue scale (VAS) measuring overall health status. Site clinicians will complete this measure during personal interviews at baseline, 6 months, 12 months, and 18 months and exit. HES, DWP and HMRC welfare payments, PNC and p-NOMIS data will be recorded from randomisation to the end of follow-up. For data modelling, we will also record these outcomes for 18-months prior to randomisation.
The schedule of enrolment, allocation, interventions and assessments is summarised in Table 1.
Following preliminary planning, we followed the DELTA2 guideline to estimate the minimum sample size for the study . Frederick and VanderWeele's meta-analysis  was used to specify the important and realistic target difference for the primary outcome, with an estimate of its uncertainty. A sensitivity calculation was included if assumptions are mis-specified.
For comparison to the duration of the IPS intervention in IPS-AD, we used the rate of competitive employment status reported by seven superiority trials which evaluated 12 months of IPS (928 participants; outcome rate 0.36 for IPS and 0.13 for TAU; odds ratio [OR] 3.76; 95% CI 2.70 to 5.24). Conservatively, we used the lower bound of the CI (i.e. 2.70; equivalent to an outcome rate of IPS 0.36 and TAU 0.18).
To achieve 90% power to detect this 18% target difference (with a two-sided 5% level of statistical significance and a 20% increase to compensate for missing or inaccurate NINO information) we estimate that 302 participants will be required with AUD and OUD (giving an expected 95% CI estimate for the OR effect within a range from 1.50 to 4.36). If the observed effect falls short of the target difference, we will be able to detect a 15% difference (which we judge is still important) with 83% power (OR 95% CI 1.24 to 3.46).
Given the lower number of people in treatment with other drug use disorders, we expect to recruit fewer participants in this group, so it will be realistic to power the analysis at 80%. For the 18% target difference (two-sided, 5% level of significance and with 20% increase for attrition), 228 participants will be needed (95% CI 1.35 to 4.57).
For the secondary outcome of total time worked, four of the seven trials used for the power calculation for the primary outcome measure in the meta-analysis reported the total number of hours worked (i.e. the sum of all time in all competitive employment during the trial). These four trials recruited 376 participants and the pooled mean difference was 505 hours (Hedges' g effect size = 0.54; 95% CI 0.33 to 0.74). Using this effect size as the realistic mean target difference, the analysis of the secondary outcome for length of competitive employment will have 99% to detect this target difference for the AUD and OUD groups. For the other drug use disorder group, we will be able to detect an effect size ranging from 0.54 to 0.38 with a minimum of 82% power.
With these conservative planning assumptions, a total of 832 participants will be the minimum number of participants required. Mediation analysis and longer-term follow-ups will benefit from a greater sample size, so recruitment is expected to extend well beyond this minimum.
Following signed terms of reference and charter respectively, an independently chaired Trial Steering Committee (TSC) and Data Monitoring Committee (DMC), will oversee study integrity, recruitment, research measure completion and analysis. These committees will include members with addiction service delivery, commissioning or IPS expertise, and patient and public involvement (PPI). The Trial Management Group will be responsible for day-to-day running of the study and members will attend meetings of the oversight committees. After approving the protocol, the TSC and DMC will meet approximately three times each year.
All serious adverse events will be promptly reported to the DMC (for the TSC) and the study sponsor. The chief investigator will have overall responsibility for the trial dataset, supported by the oversight committees. The study may be prematurely discontinued by the sponsor, or for reasons reported by the chair of the DMC to the chair of the TSC.
Information governance and data linkage
Physical case report forms will be securely stored at each site. Sites will report research data and management information securely via NDTMS. A data submission portal will transfer monthly patient information to the study. Clinical site personnel will use a two-factor authentication before access to submit data.
A bespoke Local Data Collection System (LDCS) will collect data on participant identification characteristics, scheduled and attended IPS support sessions, and self-report job data to facilitate study monitoring. LDCS will be used by the Principal Investigator and ES at each site with data sent to the study via secure file transfer. All study data will be stored in password-protected folders within a restricted area of PHE's network, accessible only by a limited number of authorised analysts. Additionally, there will be physical and other data security safeguards to protect the data, and audit processes.
The planned deterministic data linkage procedure (to be described in detail in the pre-registered analysis plan) will be based on the participant’s NINO for vocational outcomes, and NHS number for health-related outcomes. If the event of missing data, linkage will be done utilising the participant’s full first name and surname, date of birth, gender and full or partial postcode or upper-tier local authority of residence. The HES patient identifier will be used to verify that a participant has been linked to a single HES patient. Linkage with offending databases (PNC and p-NOMIS) will utilise participant’s full first name and surname, date of birth, gender and upper-tier local authority of residence. Data to enable linkage will be transferred from PHE to government departments via a strong password-protected, encrypted, file transfer protocol. This transfer and linkage protocol will be reviewed periodically and may be enhanced.
Descriptive analysis will summarise the sample in terms of demographic, clinical and vocational history characteristics. For those attaining competitive employment during the study, we will summarise their earnings and income using HMRC’s RTI system.
Primary vocational effectiveness
The SAP will be approved by the trial committees and will be published on the Open Science Framework (OSF; www.osf.io) before it is implemented after data-lock. There will be no interim analyses and specified trial stopping rules. The analysis of the primary outcome (completed in STATA or R; final code to be placed on OSF) will follow the intention-to-treat (ITT) principle and include all patients in the group to which they are allocated. Alpha will be set at 5% for the primary and secondary outcomes (with associated 95% CIs). The distributions of scale and count measures may be non-normal (skewed), so test statistics and effect sizes may be computed following appropriate transformation (e.g. natural log to obtain a geometric mean).
Data from all sites will be pooled and the superiority effectiveness estimate for the IPS intervention (adjusted OR and CI) will be determined using a mixed-effects, multi-variable logistic regression model. The model will include the stratification variables and a random intercept for each site to account for clustering. A maximum-likelihood multiple imputation approach will be used for the management of missing data with a sensitivity comparison to the complete case dataset.
Analysis of secondary vocational and alcohol and drug treatment-related outcomes
The ITT analysis of the secondary vocational and clinical outcomes will be done using appropriate mixed-effects regression models according to each measure (i.e. linear for time-based [total time in employment and treatment]; Poisson for count-based [number of appointments; days of alcohol and drug use; number of treatment episodes]; logistic for binary outcomes [sustained employment; DSM-5 remission]; ordinal for treatment exit status; and proportional-hazards [for time to first employment] with measure-appropriate covariates. These models will include site and employment history stratification factors and may include other background variables. Exploratory models will also be separately done for AUD, OUD and other drug use disorder groups. A causal mediation framework analysis will be used to determine evidence for a theoretical mechanism of change for the IPS intervention using the JSSE-B as a mediator of competitive employment.
After completing the analysis and reporting of the primary and secondary analyses, we plan to undertake exploratory longer-term analyse using the national registry data at 3 years and 6 years –subject to approval for a protocol amendment.
The HEAP will be approved by the trial committees and will be published on the OSF before data-lock. Using all primary and secondary vocational, treatment-related, social and health outcomes, the analysis will determine whether IPS has a positive net benefit and is cost-effective compared to TAU. Using a cost-benefit ratio, a primary social cost-benefit analysis (CBA) will estimate the extent of additional monetised benefits accrued by the public and the Exchequer from investing in IPS. Costs and benefits will be analysed at the patient-level, before and after exposure to IPS and TAU.
Taking an NHS and patient perspective, a secondary cost-effectiveness analysis (CEA) will compare outcomes at baseline and 18-months after trial enrolment to calculate the additional cost per quality-adjusted life year (QALY), using mortality data and utilities estimated using the EQ-5D-5L. An incremental cost-effectiveness ratio (ICER) will be estimated to determine if IPS is cost-effective from the perspective of the health and social care sectors.
Outcomes from national registries will be used to estimate net tax revenue benefits accrued to the Exchequer, along with wider societal and economic benefits, and QALY gains. Official government fiscal, economic and social monetary values will be applied to the difference in events observed pre-and post-enrolment between the control and the intervention arms. For example, hospital activity will be valued by attaching average unit costs per episode derived from the Personal Social Services Research Unit (PSSRU)  or the national reference sheet  and criminal activity will be valued using the Home Office social and economic costs of crime .
The unit costs of IPS at each site will be estimated from information from the provider on site delivery using a Staff Time Survey (STS) of direct and indirect time spent on delivering IPS and delivering research. This will be conducted on three occasions during the study (i.e. at 6 months, 12 months and 18 months) to remove noise from the data collection exercise. The unit costs of TAU (including JCP appointments) will be calculated for both the control and the intervention arms of the trial using the Universal Credit Full Service (UCFS) strategic extract for Universal Credit claimants and the DWP Labour Market System (LMS) for legacy benefit claimants. We will work towards incorporating the costs of referrals to other labour market programmes, such as the WHP, using the same data sources.
All costs will be multiplied by the market forces factor (MFF) developed by the NHS to adjust for the unavoidable geographical cost differences by site and differential labour and building costs.
The within-trial primary and secondary analysis will be conducted after all participants have been followed-up for 18 months after trial enrolment. After completing the analysis and reporting of the within-trial primary and secondary economic analyses and sensitivity checks as specified in the HEAP, we envisage undertaking an exploratory longer-term economic analysis phase of the national registry data at 3 years and 6 years, subject to approval for a protocol amendment.