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Integrated Chiropractic and Acupuncture Treatment for Low Back Pain

Effect of an Integrative Approach of Chiropractic and Traditional Chinese Medicine Care on Low Back Pain: A Randomized Controlled Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01357343
Enrollment
103
Registered
2011-05-20
Start date
2011-02-28
Completion date
2014-12-31
Last updated
2021-09-23

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

Conditions

Low Back Pain

Keywords

Low back pain, Chiropractic, Acupuncture, Integrated care

Brief summary

This study is being conducted to compare the effectiveness of integrated chiropractic and acupuncture care for the management of low back pain.

Detailed description

This study is being conducted at the Southern California University of Health Sciences. Eligible subjects will be randomized to one of three treatment groups: chiropractic care alone, acupuncture care alone, and chiropractic and acupuncture care combined. Subjects will be treated on pragmatic basis for 60 days and then followed up for an additional 60 days. All examinations and treatments will be provided free of charge. The expected benefits for the participants are decreased pain and improved function.

Interventions

Spinal manipulation and active and passive therapy.

OTHERAcupuncture

Acupuncture needling, moxa, Tui Na and cupping.

Sponsors

Southern California University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Are 18 years or older * Have a current episode of low back pain

Exclusion criteria

* Received chiropractic treatment or other manipulative therapies within the last month * Received acupuncture treatment within the last month * Visceral, systemic or joint inflammatory disease with referred pain to the back or pelvis * Non-mechanical low back pain * A history of low back surgery * Osteoporosis * Spondylolisthesis * Coagulation disorder or are taking anticoagulant medication * Prolonged systemic corticosteroid medication * Progressive unilateral lower limb muscle weakness * Symptoms or signs of cauda equina syndrome (e.g., bowel or bladder dysfunction) * Severe concurrent illness (e.g., cancer, heart diseases, psychiatric disorders) * Known pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Pain numeric rating scale.Change from baseline to 60 daysThis outcome will measure changes in the participant's level of low back pain.
Disability due to low back painChange from baseline to 60 daysWe will be using Roland-Morris scale to measure disability due to low back pain.

Secondary

MeasureTime frameDescription
Quality of lifeChange from baseline to 60 days daysQuality of life is often reduced due to low back pain. The SF-36 outcome measure will be used to determine if the treatment has any effect on quality of life of the participants.
Patient satisfaction with treatmentChange from baseline to 60 daysWe will be using Cherkin-satisfaction scale to measure patient's satisfaction with the treatment offered.
Self generated survey of outcomesChange from baseline to 60 days daysFrequency of symptoms, Medication use, Lost work time, Health services utilization

Countries

United States

Outcome results

None listed

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