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Acupressure for Fatigue and Low Back Pain

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University of Michigan

Status

Completed

Conditions

Chronic Low Back Pain
Fatigue

Treatments

Behavioral: Relaxation acupressure
Behavioral: Stimulating acupressure

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full description

Acupressure is a Traditional Chinese Medicine (TCM) technique based on a philosophy similar to that of acupuncture. It involves the application of physical pressure on different acupuncture points (acupoints). One advantage of acupressure is the ability to self-administer the treatment. Acupressure is also a viable alternative to acupuncture in situations where patients: (1) cannot come to the clinic to receive an acupuncture treatment; (2) when a more frequent intervention is needed; or (3) where needle phobia or safety concerns are an issue.

The objective of this study is to evaluate the validity and feasibility of teaching acupressure interventions using an acupressure educator for the management of symptoms related to low back pain.

Specific aims:

  1. To examine the effect of 6-weeks of relaxation acupressure (RA) compared to a regime of stimulating acupressure (SA) or wait-list control (WL) on fatigue and sleep quality as assessed by Brief Fatigue Inventory and wrist-worn accelerometry (sleep efficiency).
  2. To explore the effect of 6-weeks of RA compared to a regime of SA or WL on for chronic low back pain in terms of reduced pain and improved function.

Enrollment

51 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

51 participants in 3 patient groups

Relaxation acupressure
Experimental group
Treatment:
Behavioral: Relaxation acupressure
Stimulating acupressure
Active Comparator group
Treatment:
Behavioral: Stimulating acupressure
Wait-list control
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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