# UCSF Core Center for Patient-centric Mechanistic Phenotyping in Chronic Low Back Pain

> **NIH NIH U19** · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · 2020 · $104,939

## Abstract

1 Project Summary
 2 Low back pain is predicted to affect 80% of the general population at some point in their lifetime. Chronic low
 3 back pain (cLBP), the most common non-cancer reason for opioid use, is particularly difficult to diagnose and
 4 treat effectively, in part, due to the interconnected biophysical and psychosocial factors which complicate the
 5 relationship between impairment, disability, and pain related to cLBP. The biopsychosocial model posits that
 6 signals from noxious stimuli are modulated by mental, emotional, and sensory mechanisms that are, in turn,
 7 influenced by psychological and social factors. Maladaptive pain cognitions (fear of movement and pain
 8 catastrophizing) can lead to compensatory movement patterns that directly affect movement biomechanics and
 9 paraspinal muscle (PSM) structure and function, driving further impairment, disrupting the balance between
10 passive and active spine stabilizers, and reinforcing the patient’s perceived disability status. This cyclic
11 relationship between biophysical and psychological factors likely plays a critical role in the manifestation of pain
12 and disability in cLBP. A better understanding of this relationship will inform the identification of
13 interventional phenotypes in cLBP and provide clinicians with better tools for the development of
14 effective and patient-specific diagnosis and treatment plans. This has important implications towards
15 identifying cLBP subgroups that would be better served with physical and/or cognitive therapies, providing an
16 alternative to pharmaceutical interventions. To clarify the relationship between biophysical and psychological
17 factors in cLBP, we will investigate 1) how psychological factors, spinal pathology, and patient perception of pain
18 severity and disability status influence compensatory movement strategies 2) how movement biomechanics,
19 psychological factors, and pain mechanisms relate to PSM quality and 3) how movement biomechanics and
20 PSM quality change over time in relation to psychological factors, pain mechanism, pain severity, and prescribed
21 treatment plan. We hypothesize that 1) maladaptive pain cognitions will have more influence on movement
22 biomechanics and pain-related outcomes over time than biophysical factors and 2) baseline measures of
23 psychological and biophysical factors will be predictive of pain-related outcomes
24 For the training aspect of this study, I will work closely with pain management clinicians, clinical pain
25 researchers, physical therapists, patient advocates, and engineers who will guide my training and provide
26 necessary resources and experiences driving my development toward independence as a clinical pain
27 researcher. I will develop fundamental skills in clinical pain research through coursework in biostatistics and pain
28 assessment and programs on writing grants and publications. Through this structured research experience and
29 training plan, I will le...

## Key facts

- **NIH application ID:** 10208515
- **Project number:** 3U19AR076737-01S1
- **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
- **Principal Investigator:** JEFFREY C. LOTZ
- **Activity code:** U19 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $104,939
- **Award type:** 3
- **Project period:** 2019-09-25 → 2024-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10208515

## Citation

> US National Institutes of Health, RePORTER application 10208515, UCSF Core Center for Patient-centric Mechanistic Phenotyping in Chronic Low Back Pain (3U19AR076737-01S1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10208515. Licensed CC0.

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