Acupressure for Fatigue and Low Back Pain
Completed · Not applicable
Conditions studied: Fatigue, Chronic Low Back Pain
In brief
The purpose of this study is to compare two kinds of self-administered acupressure (relaxation acupressure and stimulating acupressure) to usual care for management of fatigue and pain in low back pain patients. Hypothesis: Self-administered relaxation acupressure will result in improvements in fatigue and sleep quality, pain, and physical function compared to stimulating acupressure and usual care.
Key facts
- Study ID
- NCT02106741
- Run by
- University of Michigan
- People needed
- 51
- Starts
- 2013-05-01
- Expected to finish
- 2016-05-01
- Last updated by the study team
- 2016-10-25
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Aged18-65 years
- Non-specific low back pain (either by self-report or via ICD-9 codes 724.2, 724.5, 846.0-846.9)
- Low back pain that has persisted for at least 3 months
- Minimum of 3/10 on the Pain Bothersome Scale
- Minimum of 3/10 fatigue severity
- Ambulatory with or without assistive device
- Ability to operate the accelerometer (Actiwatch-S)
- Stable medication regiment for the previous 2 months
- Report of a physician's visit during the previous 24 months
- English-speaking
You may not qualify if…
- Medically unstable (acute conditions or acute presentations of chronic conditions)
- Current pregnancy
- Radiculopathy or report of low back pain radiating to below the knee
- Reported history of spinal fracture, herniated lumbar disc, ankylosing spondylitis, and spinal stenosis.
- Report of back surgery within the preceding 12 months
- Participation in active litigation or compensation claims
- Conditions that might confound treatment effects or interpretation of results (for example, rheumatoid arthritis, lupus)
- Acupuncture or acupressure within the preceding 12 months
- Report of sleep apnea
- 2nd or 3rd shift workers or other non-traditional sleep schedules
- Use of anti-coagulant/platelet therapy within the preceding month
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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