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Remotely Delivered Yoga Program for Chronic Low Back Pain

Feasibility of a Remotely Delivered Yoga Intervention for Chronic Low Back Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04773743
Enrollment
10
Registered
2021-02-26
Start date
2021-02-15
Completion date
2021-07-30
Last updated
2021-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

chronic pain, yoga, meditation

Brief summary

The purpose of this research is to integrate the meditative components of integrative restoration (iRest) yoga nidra with simple and safe movement sequences derived from established yoga postures and physical therapy interventions for chronic nonspecific low back pain and to use telemedicine technology to facilitate the intervention in a diverse socioeconomic and racial/ethnic population. This project will first systematically adapt the iRest yoga intervention for the incorporation of movement using a consultative and iterative process followed by a pilot intervention to assess the acceptability and preliminary efficacy of this program for pain, back related function and to address body-mind regulation and biopsychosocial-spiritual well-being. Hypothesis: a yoga intervention emphasizing meditative movement and relaxation will be safe for remote delivery and effective for biopsychosocial-spiritual outcomes for people with chronic low back pain.

Interventions

OTHERYoga

Remotely delivered yoga intervention

Sponsors

University of Maryland, College Park
CollaboratorOTHER
Maryland University of Integrative Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Adults age 18-64 years who report chronic nonspecific low back pain, defined as low back pain of unknown etiology persisting for at least 12 weeks, * Participants must report an average pain intensity in the previous week of 4 or greater on an 11-point (0 to 10) numerical rating scale, * Demonstrate medium to high risk on the STarT back screening tool, * Understand English * Have access to technology including a computer and internet access

Exclusion criteria

* Specific causes of low back pain (e.g. spinal fractures, cancer-related pain) * Severe or progressive neurological deficits * Severe chronic medical and/or psychiatric comorbidities that may prevent safe participation in the study * Established pregnancy * Current yoga practice or regular yoga class attendance in the last three months; * Current application for a receipt of workers compensation * lack of access to technology including a computer and the internet

Design outcomes

Primary

MeasureTime frameDescription
Change in Oswestry Disability IndexPre, midpoint (4 weeks), final (8 weeks), 1 month follow upBack related function and pain

Secondary

MeasureTime frameDescription
Change in Vagal EfficiencyPre, midpoint (4 weeks), final (8 weeks), 1 month follow upA device will be used to measure Heart rate variability and vagal efficiency
Change in Purpose in LifePre, midpoint (4 weeks), final (8 weeks), 1 month follow upSix item measure of purpose in life
Change in Body Brain Center Sensory ScalesPre, midpoint (4 weeks), final (8 weeks), 1 month follow upSubjective measure of sensory sensitivity
Change in Body Perception Questionnaire subscale on autonomic reactivityPre, midpoint (4 weeks), final (8 weeks), 1 month follow upSubjective measure of autonomic reactivity

Contacts

Primary ContactMarlysa Sullivan, MPT
msullivan1@muih.edu4108889048

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026