Improving Health for Patients With Chronic LBP in Rural Communities Through Telerehabilitation
- Conditions
- Chronic Low-back Pain
- Interventions
- Behavioral: Educational ControlBehavioral: Telerehabilitation
- Registration Number
- NCT06471920
- Lead Sponsor
- Johns Hopkins University
- Brief Summary
Physical therapy is the first line of treatment for patients with low back pain (LBP) and has been shown to be a cost-effective method for improving pain and disability in patients with chronic LBP; however, despite this effectiveness, only 7-13% of patients go on to receive physical therapy services with patients in rural communities being especially limited to do lack of provider availability, transportation, and missed work time leading to greater rates of LBP-related disability and opioid consumption. With the rapid emergence of digital treatment approaches to physical therapy (i.e., telerehabilitation), access could be improved by reducing or eliminating many barriers that patients report; however, it is unclear how to appropriately incorporate digital treatment approaches into existing health care models. The investigators propose a prospective randomized clinical trial conducted at a health system serving rural communities to determine the effectiveness of innovative risk-informed telerehabilitation versus standard educational control for patients with chronic LBP that will match individual patients with specific physical therapy delivery (physical therapy telehealth visits or psychologically informed physical therapy telehealth visits) based on the patient's psychosocial risk of poor outcomes.
- Detailed Description
Chronic low back pain (LBP) imposes tremendous burden on affected individuals, healthcare systems, and society. LBP has been identified as the most common cause of disability globally and in the United States (US). LBP is also the largest driver of US healthcare spending ($135 billion in 2016) and the most common diagnoses associated with opioid prescription and consumption. For patients with chronic LBP, physical therapy has been shown to be a cost-effective method for improving pain and disability. In addition, physical therapy has been shown to decrease the risk of advanced imaging, injections, surgery, and opioid use in patients with chronic LBP.
Despite available evidence in support, only 7-13% of patients with LBP, including those with chronic LBP, go on to receive physical therapy services, with patients reporting barriers accessing physical therapy, such as transportation, provider availability and missed work time. Access is especially limited in rural communities where there are approximately 40% fewer physical therapists available per capita compared to metropolitan regions. In addition, patients living in rural communities likely need to travel longer distances to receive physical therapy, requiring additional missed work time and transportation costs. This lack of access to physical therapy in rural communities likely contributes to the greater rates of LBP-related disability and opioid consumption that have been observed in rural communities compared to metropolitan areas. Innovative methods for improving access to physical therapy are urgently needed to address disparities in outcomes for patients with chronic LBP living in rural communities in the US. Telehealth has rapidly expanded during the COVID-19 pandemic. This includes policy changes that have allowed physical therapists to begin providing care remotely, also referred to as telerehabilitation. Telerehabilitation stands to improve access to physical therapy for patients with chronic LBP living in rural communities and may serve as a means of improving outcomes of these patients.
The investigators will conduct a prospective randomized clinical trial addressing key questions to understanding the effectiveness of a risk-informed telerehabilitation to reduce opioid use and LBP-related disability and to improve physical function and health-related quality of life (HRQoL) in patients with chronic LBP. Additionally, the investigators will explore implementation outcomes using a mixed methods approach consisting of electronic surveys and semi-structured interviews with patients, physical therapists, practice managers, and outpatient services administration focusing on perceived quality and impact on barriers to care. The investigators will enroll 434 patients with LBP presenting to primary care clinics serving rural communities (TidalHealth, Salisbury, MD). Eligible patients will provide informed consent and be randomized to either web-based standardized education or risk-informed telerehabilitation (physical therapy telehealth visits, or informed physical therapy telehealth visits). Primary effectiveness outcome is difference in change in LBP-related disability (Oswestry Disability Index) and in opioid use after 8 weeks of treatment.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 434
- Primary care visit in the past 90 days with an LBP-related International Classification of Diseases (ICD-10) diagnosis.
- Age 18 years or older.
- At least moderate levels of pain and disability requiring Oswestry score ≥24% and average pain rating ≥ 4/10 points.
- Meets NIH Task Force2 definition of chronic LBP based on two questions: 1) How long has LBP has been an ongoing problem? and 2) How often has LBP been an ongoing problem over the past 6 months? A response of greater than 3 months to question 1, and "at least half the days in the past 6 months" to question 2 is required to satisfy the NIH definition of chronic LBP.
- Can speak and understand English.
- Access to video-enabled device and Internet.
- Recent history (last 6 months) of lumbar spine surgery.
- Possible non-musculoskeletal cause for low back pain symptoms (e.g., pregnancy).
- Evidence of serious pathology as a cause of LBP including neoplasm, inflammatory disease (e.g., ankylosing spondylitis), vertebral osteomyelitis, etc.
- Neurological disorder resulting in severe movement disorder, or schizophrenia or other psychotic disorder.
- Knowingly pregnant.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Educational Control Educational Control Patients randomized to the educational control group will receive registered access to a study website with access to evidence-based education for patients with chronic LBP. Each participant will have unique login credentials to allow for tracking of individual patient use. The website will include important education on the etiology of chronic LBP and evidence-based suggestions for self-management of symptoms. Education will focus on the importance of maintaining healthy levels of physical activity and avoiding bedrest. To promote increased physical activity levels, the website will also include pictures and videos of common exercises targeting the lumbopelvic region that patients can perform independently without the need for exercise equipment. Telerehabilitation Telerehabilitation Based on prior STarT Back Tool (SBTS) screening risk stratification, participants in the risk-informed telerehabilitation group will receive subsequent care using an evidence-based treatment protocol designed for video visits to be informed by a participant's baseline risk score with elements ranging from standard physical therapy telehealth visits (low-to-medium risk) to psychological informed physical therapy (PIPT) telehealth visits (high-risk). The SBTS is a short questionnaire that assesses an individual's physical, psychosocial, and psychological risk factors for chronic back pain that can be improved with treatment.
- Primary Outcome Measures
Name Time Method Change in Oswestry Disability Index Change from baseline to 12 weeks after treatment initiation LBP-related disability. The total score range is \[0, 100\] with higher values representing greater pain-related disability.
- Secondary Outcome Measures
Name Time Method Participants with Opioid Use Post treatment initiation 12 weeks self-reported and/or Electronic Health Record (EHR) documented opioid use
Change in Patient-Reported Outcomes Measurement Information System (PROMIS-29) Physical Function Change from baseline to 26- and 52-weeks after treatment initiation Physical function. The total score range is \[0, 100\] with higher scores indicating better physical function.
Change in Patient-Reported Outcomes Measurement Information System (PROMIS-29) Physical Function by Gender Change from baseline to 26- and 52-weeks after treatment initiation Physical function. The total score range is \[0, 100\] with higher scores indicating better physical function.
Change in Patient-Reported Outcomes Measurement Information System (PROMIS-29) Physical Function by Age Group Change from baseline to 26- and 52-weeks after treatment initiation Physical function. The total score range is \[0, 100\] with higher scores indicating better physical function.
Change in Patient-Reported Outcomes Measurement Information System (PROMIS-29) Physical Function by Baseline Opioid Use Change from baseline to 26- and 52-weeks after treatment initiation Physical function. The total score range is \[0, 100\] with higher scores indicating better physical function.
Change in PROMIS Preference Score (PROPr) Change from baseline to 26- and 52-weeks after treatment initiation Total score range is \[0, 100\] with higher scores indicating better outcome.
Change in PROMIS Preference Score (PROPr) by Gender Change from baseline to 26- and 52-weeks after treatment initiation Total score range is \[0, 100\] with higher scores indicating better outcome.
Change in PROMIS Preference Score (PROPr) by Age Group Change from baseline to 26- and 52-weeks after treatment initiation Total score range is \[0, 100\] with higher scores indicating better outcome.
Change in PROMIS Preference Score (PROPr) by Baseline Opioid Use Change from baseline to 26- and 52-weeks after treatment initiation Total score range is \[0, 100\] with higher scores indicating better outcome.
Percent of participants using non-opioid LBP-Related Healthcare Use 26- and 52-weeks after treatment initiation Non-opioid LBP-related healthcare use (e.g., physician office visit, imaging, surgery)
Percent of participants using non-opioid LBP-Related Healthcare Use by Gender 26- and 52-weeks after treatment initiation Non-opioid LBP-related healthcare use (e.g., physician office visit, imaging, surgery)
Percent of participants using non-opioid LBP-Related Healthcare Use by Age Group 26- and 52-weeks after treatment initiation Non-opioid LBP-related healthcare use (e.g., physician office visit, imaging, surgery)
Percent of participants using non-opioid LBP-Related Healthcare Use by Baseline Opioid Use 26- and 52-weeks after treatment initiation Non-opioid LBP-related healthcare use (e.g., physician office visit, imaging, surgery)
Trial Locations
- Locations (2)
Johns Hopkins University School of Medicine
🇺🇸Baltimore, Maryland, United States
Tidalhealth
🇺🇸Salisbury, Maryland, United States