MRC Versus Arthritis Centre for Musculoskeletal Health and Work, University of Southampton, Southampton General Hospital, Southampton, UK.
MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton, UK.
Health Technol Assess. 2021 Jan;25(5):1-72. doi: 10.3310/hta25050.
Chronic pain is a common cause of health-related incapacity for work among people in the UK. Individualised placement and support is a systematic approach to rehabilitation, with emphasis on early supported work placement. It is effective in helping people with severe mental illness to gain employment, but has not been tested for chronic pain.
To inform the design of a definitive randomised controlled trial to assess the clinical effectiveness of individualised placement and support for people unemployed because of chronic pain.
A mixed-methods feasibility study comprising qualitative interviews and focus groups with key stakeholders, alongside a pilot trial.
Primary care-based health-care professionals, employment support workers, employers, clients who participated in an individualised placement and support programme, and individuals aged 18-64 years with chronic pain who were unemployed for at least 3 months.
An individualised placement and support programme integrated with a personalised, responsive pain management plan, backed up by communication with a general practitioner and rapid access to community-based pain services.
Outcomes included stakeholder views about a trial and methods of recruitment; the feasibility and acceptability of the individualised placement and support intervention; study processes (including methods to recruit participants from primary care, training and support needs of the employment support workers to integrate with pain services, acceptability of randomisation and the treatment-as-usual comparator); and scoping of outcome measures for a definitive trial.
All stakeholders viewed a trial as feasible and important, and saw the relevance of employment interventions in this group. Using all suggested methods, recruitment was feasible through primary care, but it was slow and resource intensive. Recruitment through pain services was more efficient. Fifty people with chronic pain were recruited (37 from primary care and 13 from pain services). Randomisation was acceptable, and 22 participants were allocated to individualised placement and support, and 28 participants were allocated to treatment as usual. Treatment as usual was found acceptable. Retention of treatment-as-usual participants was acceptable throughout the 12 months. However, follow-up of individualised placement and support recipients using postal questionnaires proved challenging, especially when the participant started paid work, and new approaches would be needed for a trial. Clients, employment support workers, primary care-based health-care professionals and employers contributed to manualisation of the intervention. No adverse events were reported.
Unless accurate and up-to-date employment status information can be collected in primary care health records, or linkage can be established with employment records, research such as this relating to employment will be impracticable in primary care. The trial may be possible through pain services; however, clients may differ. Retention of participants proved challenging and methods for achieving this would need to be developed. The intervention has been manualised.
Current Controlled Trials ISRCTN30094062.
This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in ; Vol. 25, No. 5. See the NIHR Journals Library website for further project information.
在英国,慢性疼痛是导致人们工作相关能力丧失的常见原因。个体化安置和支持是一种系统的康复方法,强调早期支持性工作安置。它在帮助患有严重精神疾病的人就业方面非常有效,但尚未针对慢性疼痛进行测试。
为一项评估个体化安置和支持对因慢性疼痛而失业的人的临床有效性的决定性随机对照试验提供信息。
一项混合方法可行性研究,包括与主要利益相关者进行定性访谈和焦点小组,以及一项试点试验。
在初级保健基础上的医疗保健专业人员、就业支持工作者、雇主、参加个体化安置和支持计划的参与者,以及年龄在 18-64 岁之间因慢性疼痛失业至少 3 个月的人。
个体化安置和支持计划与个性化、响应式疼痛管理计划相结合,由与全科医生的沟通和快速获得社区疼痛服务支持。
所有利益相关者都认为试验是可行且重要的,并认为在这一群体中进行就业干预是相关的。通过所有建议的方法,通过初级保健进行招募是可行的,但速度较慢且资源密集。通过疼痛服务进行招募更有效。共招募了 50 名慢性疼痛患者(37 名来自初级保健,13 名来自疼痛服务)。随机分组是可以接受的,22 名参与者被分配到个体化安置和支持组,28 名参与者被分配到常规治疗组。常规治疗是可以接受的。在 12 个月的时间里,常规治疗组参与者的保留率是可以接受的。然而,通过邮寄问卷对个体化安置和支持接受者进行随访证明具有挑战性,尤其是当参与者开始带薪工作时,需要采用新的方法进行试验。客户、就业支持工作者、初级保健医疗保健专业人员和雇主为干预措施的手册化做出了贡献。没有报告不良事件。
除非在初级保健医疗记录中可以收集到准确和最新的就业状况信息,或者可以与就业记录建立联系,否则与就业相关的此类研究在初级保健中是不可行的。通过疼痛服务可能可以进行试验;然而,客户可能会有所不同。参与者的保留率具有挑战性,需要开发相关方法。干预措施已经手册化。
当前对照试验 ISRCTN30094062。
本项目由英国国家卫生研究院(NIHR)健康技术评估计划资助,将在 ;第 25 卷,第 5 期全文发表。有关该项目的更多信息,请访问 NIHR 期刊库网站。