Abstract
Background: Access to greenspace (eg, parks) may improve aspects of physical and mental health that are known biopsychosocial contributors to back pain. However, little is known about the association between access to greenspace and back pain. Methods: This cross-sectional analysis used data from the Study of Osteoporotic Fractures (SOF) and the Osteoporotic Fractures in Men Study (MrOS) to investigate the association of proximity to greenspace with back pain among community-dwelling older adults living in Portland, Oregon, USA. Geospatial software characterized proximity to greenspace (distance from residential address to nearest park) into three categories thought to be relevant for walkability among older adults: <0.125, 0.125–0.5, and >0.5 mile. We estimated the crude prevalence of any back pain (yes/no) during the past year by proximity-to-greenspace categories and their association as gender-specific prevalence ratios (aPRs) using log-binomial regression models adjusted for age, race, education, and neighborhood socioeconomic status. Results: Participants were 1839 SOF women (mean age = 74.6 years, SD = 5.3) and 422 MrOS men (mean age = 73.7 years, SD = 5.8). Living >0.5 mile from a park, compared to living <0.125 mile, was associated with a greater prevalence of back pain among women (crude prevalence: 71.1% vs. 61.6%, aPR = 1.15 [1.02–1.29]) but not men (64.2% vs. 76.4%, aPR = 0.82 [0.66–1.02]). Sensitivity analyses that used more severe back pain phenotypes provided heterogenous results. Conclusion: In this cross-sectional study, living near a park was associated with a modestly lower prevalence of back pain for women but not men. Large prospective studies are needed to further evaluate whether living close to parks, or other greenspaces, is associated with back pain in older adults.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | PM&R |
| ISSN | 1934-1482 |
| DOI | |
| Status | E-pub ahead of print - 19. aug. 2026 |
Finansiering
The Study of Osteoporotic Fractures (SOF) is supported by National Institutes of Health funding. The National Institute on Aging provides support under the following grant numbers: R01AG028254, R01AG005407, R01AR35582, R01AR35583, R01AR35584, R01AG005394, R01AG027574, and R01AG027576. The Osteoporotic Fractures in Men (MrOS) Study is also supported by the following institutes provide support: the National Institute on Aging, the National Institute of Arthritis and Musculoskeletal and Skin Diseases, the National Center for Advancing Translational Sciences, and National Institutes of Health Roadmap for Medical Research under the following grant numbers: R01AG026002, U01AG027810, U01AG042124, U01AG042139, U01AG042140, U01AG042143, U01AG042145, U01AG042168, U01AR066160, R01AG066671, and UL1TR000128. Dr Roseen is the recipient of a career development award from the National Center for Complementary and Integrative Health (K23AT010487), which supported his work on this manuscript. Dr Mu is supported through training grants from the National Heart, Lung, and Blood Institute (F31HL165898) and the National Institute on Aging (T32AG049663). Dr Jessica Wong is supported by a Canadian Institutes of Health Research Research Excellence, Diversity and Independence Early Career Transition Award. Dr Pescador Jimenez receives support by National Institute on Aging under grant numbers: R00AG066949, R01AG087199, R01NS139186. Dr Michael receives support by National Institute on Aging under grant number: R01AG072634.
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