Low Back Pain, Mechanical Clinical Trial
Official title:
Comparison Between Pragmatically Applied Orthopedic Manual Therapy and Dry Needling for Low Back Pain.
Both orthopedic manual therapy (OMT) and dry needling (DN) have been shown to be effective at reducing pain and disability for individuals with low back pain (LBP). It is unclear if one intervention, or in combination with one another, is more effective. The purpose of this randomized clinical trial is to determine the clinical effectiveness of OMT or DN alone compared with combined OMT + DN on pain and disability for patients with LBP. Both within and between group effects will be presented. Patient factors such as; generalized anxiety disorder, depression, fear-avoidance behaviors, pain catastrophizing, and sleep-quality have negatively correlated with pain and disability outcomes in patients experiencing chronic LBP. Moreover, sleep deprivation and pain related fear of movement functionally can change a person's pain inhibitory pathways leading to hyeralgesia. These factors have been individually analyzed regarding their effects on pain related outcomes, which limits our understanding of how clustering patient factors might affect recovery. A secondary aim will involve determining the relationship between patient factors and clinical outcomes for individuals with LBP who receive DN and/or manual therapy.
Status | Not yet recruiting |
Enrollment | 188 |
Est. completion date | December 2025 |
Est. primary completion date | December 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients who are 18 years of age or older, present with LBP and a pain score of > or = 3/10 Exclusion Criteria: - Patients will be excluded if they present with a contraindication to either treatment (malignancy, fracture, myelopathy, osteoporosis, etc.), have a prior surgical history involving the lumbar spine, present with spinal nerve root compression (2 or more neurological findings that includes myotome weakness, dermatomal sensory loss, and/or deep tendon reflexive changes), are seeking litigation, or are receiving other forms of conservative care. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Youngstown State University | Duke University |
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Hu HT, Gao H, Ma RJ, Zhao XF, Tian HF, Li L. Is dry needling effective for low back pain?: A systematic review and PRISMA-compliant meta-analysis. Medicine (Baltimore). 2018 Jun;97(26):e11225. doi: 10.1097/MD.0000000000011225. — View Citation
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Rubinstein SM, de Zoete A, van Middelkoop M, Assendelft WJJ, de Boer MR, van Tulder MW. Benefits and harms of spinal manipulative therapy for the treatment of chronic low back pain: systematic review and meta-analysis of randomised controlled trials. BMJ. 2019 Mar 13;364:l689. doi: 10.1136/bmj.l689. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Patient Treatment Preference | The patient rates their preference for treatment between dry needling, orthopedic manual threrapy, or both. | Baseline | |
Other | Clinician Treatment Preference | The clinician rates their preference for treatment between dry needling, orthopedic manual threrapy, or both. | Baseline | |
Other | Credibility Expectancy Questionnaire | Scale for measuring treatment expectancy and rationale credibility for use in clinical outcome studies. | Baseline | |
Primary | PROMIS-29.2 | Questionnaire that assesses 7 domains with 4 questions with an additional pain intensity numeric rating scale (NPRS). The PROMIS measures have been tested and validated in large reference populations making them suitable for research on different conditions. | Baseline, 1 week, 1 month, and 6 months | |
Secondary | Global Rating of Change | Questionnaire that assesses the global degree of change the patient perceives since the start of care.
The patient rates their change from 0 (no change) to +7 (A Very Great Deal Better) to -7 (A Very Great Deal Worse) |
1 week, 1 month, and 6 months | |
Secondary | Global Rating of Change for Medication Intake | Questionnaire that assesses the global degree of change in pain medication the patient experienced since the start of care. The patient rates their change in medications from 0 (no change) to +7 (A Very Great Deal Less) to -7 (A Very Great Deal More) | 1 week, 1 month, and 6 months | |
Secondary | Health Care Utilization | Patients will report any providers they had to see after the completion of the study to 6 months for their low back problem. | 6 months |
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