Implementation of a Stratified Model of Care for Low Back Pain Patients in Primary Care Settings
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 175
- 试验地点
- 1
- 主要终点
- Low back Pain Disability will be assessed through the Roland Morris Disability Questionnaire (RMDQ)
研究概览
简要总结
The SPLIT project evaluates the implementation of a stratified model of care for people with low back pain patients who consulted primary care.This involves evaluating the process of implementation as well as patient level outcomes.
The project consists of two phases: First, a before-after study comprising two sequential but independent cohort studies will be conducted to compare the outcomes and cost-effectiveness of current practice with the SPLIT stratified model of care. Second, an implementation strategy will be developed based on the results of a survey regarding determinants of current practice, and two focus groups concerning the barriers and facilitators for the implementation of the SPLIT stratified model of care.
详细描述
A before after study consisting of two sequential but independent cohorts of LBP patients, separated by a 3 months interval will be conducted in 6 primary care units in Portugal. In both cohorts participants will be recruited during a 7 months period.
Recruitment and data collection procedures will be identical for both cohorts. Participants will be eligible if they consult one of the participating General Practitioner practices (GA) due to non-specific Low Back Pain (LBP), with or without leg pain (The International Classification for Primary Care-2 diagnostic codes L03, L84, and L86), if they are aged between 18 and 65 years and able to read and speak the Portuguese language. They will be excluded if they have clinical signs of infection, tumor, osteoporosis, fracture, structural deformity, inflammatory disorder, radicular syndrome, or cauda equine syndrome, if they have severe depression or other psychiatric condition, if they are pregnant, or if they have undergone back surgery or conservative treatment in the prior 6 and 3 months, respectively.
Patients will be recruited by their GP, who will briefly explain the study and obtain consent to pass the contact details to a research assistant (RA). The RA will inform the patients about the study and ask them if they are willing to participate and to be contacted for follow-up questionnaires (by phone), and whether they give permission for their LBP medical records to be reviewed. Patients who decline referral will not be eligible for the study and will follow the usual clinical care.
On the initial screening with the RA, eligible LBP patients who consent to participate in the study will fill a questionnaire booklet containing socio-demographic and clinical questions, the Start Back Screening Tool, and patient reported outcomes concerning back-related disability (Roland Morris Disability Questionnaire), pain intensity (Numeric Pain Rating Scale), and health related quality of life (EuroQuol, five dimensions, 3 levels). These outcomes will be reassessed at 2 and 6 months following the first medical consultation. A Global Perceived Effect Scale (GPES) to assess patient overall perception of improvement with treatment will be added in the follow-up reassessments.
In both cohorts no specific instruction will be given to GPs concerning their practice. They will be encouraged to assess and treat their patients as usually and make all the referrals they think are appropriate for their patients. At the end of each cohort the GPs medical records will be reviewed and data concerning the number of primary care consultations, prescribed medications, ordering of diagnostic tests, referrals to other professionals or services will be extracted.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of Low back Pain of any duration;
- •Age between 18 and 65 years;
- •Able to read and speak the Portuguese language.
排除标准
- •Clinical signs of infection;
- •Clinical signs of tumor;
- •Clinical signs of osteoporosis;
- •Clinical signs of fracture;
- •Clinical signs of structural deformity;
- •Clinical signs of inflammatory disorder;
- •Clinical signs of radicular syndrome;
- •Clinical signs of cauda equine syndrome;
- •Clinical signs of severe depression or other psychiatric condition;
- •Pregnant women;
- •Patients that undergone a back surgery in the prior 6 months;
- •Patients that received any type of conservative treatment in the prior 3 months.
研究组 & 干预措施
Stratified Model of Care
A subgrouping tool helps guide clinical decision-making about treatment and onward referral (Start Back Screening Tool). Patients in each subgroup (low, medium or high risk of chronicity) are then managed according to a targeted treatment system of increasing complexity.
干预措施: SPLIT Stratified Model of Care (Other)
Usual Care
All patients were referred for the study by their General Practitioner (GP). GPs were encouraged to assess and treat their patients as usual and make all the referrals they think are appropriate for their patients.
干预措施: Usual Care (Drug)
结局指标
主要结局
Low back Pain Disability will be assessed through the Roland Morris Disability Questionnaire (RMDQ)
时间窗: Change on disability from baseline to 2 and 6 months
The RMDQ consists of 24 items that measures the functional status over the past 24 hours in patients with LBP. Each answer can be scored "0" or "1", thus leaving a range of scores from 0 to 24, with higher scores indicating higher disability. The RMDQ has shown good validity and test-retest reliability with reported intraclass correlation coefficients (ICC) of 0.8 or more.
次要结局
- Pain intensity will be assessed through the Numeric Pain Rating Scale (NPRS)(Change on pain intensity from baseline to 2 and 6 months)
- Health related Quality of life (HRQoL) will be assessed by the EuroQuol 5 dimensions, 3 levels (EQ-5D-3L) questionnaire.(Change on HRQoL from baseline to 2 and 6 months)
- Number of medical appointments for a low back pain complaint(The number of medical appointments concerning of each participant will be collected during the 6 months period after patient's enrollment)
- The rate of imaging tests prescribed related with a low back pain complaint(The number of imaging tests prescribed will be collected during the 6 months period after patient's enrollment)
- Patients perception of global change will be assessed by the questionnaire Global Perceived Effect Scale(Global perception of change related with low back condition at 2 and 6 months follow-ups)
- The rate of pain medication for low back pain complaints(The low back pain medication will be collected during the 6 months period after patient's enrollment)
研究者
Eduardo B. Cruz
Principal Investigator Eduardo José Brazete Carvalho Cruz
Instituto Politécnico de Setúbal
