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Acupuncture for Chronic Low Back Pain in Older Adults (BackInAction)

Kaiser Permanente logo

Kaiser Permanente

Status

Completed

Conditions

Chronic Low-back Pain

Treatments

Procedure: Enhanced Acupuncture
Procedure: Standard Acupuncture

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04982315
BackInAction
UH3AT010739 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The main goal of the BackInAction research study is to determine the effectiveness of a standard course of acupuncture (15 sessions of acupuncture over 3 months) and an enhanced course of acupuncture (an additional 6 sessions of acupuncture over months 4-6) in improving back-related disability in older adults (65+ years) with chronic low back pain compared to usual care alone. Key secondary aims are to determine the effectiveness of acupuncture in improving a composite score of pain intensity and pain interference.

Full description

Background: A critical gap exists in evidence regarding the safety and effectiveness of treatments for older adults (65+ years) with chronic low back pain. Acupuncture has been found to be effective in treating chronic low back pain in younger adults. Yet trials have rarely included older adults, who have more comorbidities and may respond differently than typical trial participants. BackInAction has been designed to address this gap.

Purpose: The main goal of BackInAction is to evaluate the effectiveness of a standard course of acupuncture (up to 15 sessions of acupuncture over 3 months) and an enhanced course of acupuncture (up to an additional 6 sessions of acupuncture over months 4-6) in improving back-related disability in older adults with chronic low back pain compared to usual care alone. Key secondary aims are to determine the effectiveness of acupuncture in improving a composite score of pain intensity and pain interference.

Design and Outcomes: In this pragmatic, three-arm parallel groups multi-site randomized controlled trial, the investigators will recruit and randomize at least 789 adults ≥ 65 years of age with chronic low back to standard acupuncture, enhanced acupuncture, or usual medical care alone in four health-care systems. These include two integrated health care systems, a fee-for-service system and a network of federally qualified health centers. Primary outcome data will be collected by questionnaire at 3-, 6-, and 12-months post-randomization. In addition, short monthly surveys will capture data on physical function and a composite score of pain intensity and pain interference.

Interventions and Duration: Standard acupuncture will consist of 3 months (90 days) of acupuncture needling, with a proposed minimum of 8 treatments and a maximum of 15. Enhanced acupuncture will include the standard acupuncture plus an additional 3-month maintenance period, with a maximum of six additional treatments. Usual medical care will consist of the care that individuals receive according to their insurance benefits plus anything else they pay for out of pocket. The investigators will ask those assigned to usual medical care to avoid acupuncture for the year they are enrolled in the study. Both active treatment arms will also have access to usual medical care. Participants will be enrolled in the study for 12 months.

Sample Size and Population: BackInAction will include patients at least 65 years of age with uncomplicated chronic low back pain with or without radiculopathy. The investigators plan to enroll at least 789 participants (263 per study arm). Participants will be recruited from four health plans, with varying numbers of participants from each site. Randomization will be stratified by health care system, age category and gender. The investigators expect the racial and ethnic mix will roughly parallel that of the older Medicare population.

Enrollment

807 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Is at least 65 years of age
  • Is a current member or patient of the healthcare system
  • Visited a health care provider for low back pain within the past 12 months
  • Received primary care at one of the participating health care systems
  • Has back pain that is uncomplicated with or without radicular pain
  • Back pain at least 3 months
  • General activity question from PEG (Pain, Pain Interference with Enjoyment, General Activity scale) at least 3
  • Primary care provider provides permission to contact patient
  • Willing and able to provide consent (Callahan cognitive impairment screener at least 3)

Exclusion criteria

  • Specific types of back pain (metastatic cancer or bone cancer or secondary cancers, vertebral fractures, spinal infection, active inflammatory disease)
  • Low back surgery within past 3 months
  • Receiving workers compensation or involved in litigation related to chronic low back pain
  • Acupuncture within the last 6 months
  • Does not speak or write English or Spanish
  • Major psychosis, dementia
  • Current cancer treatment
  • Red flags of serious underlying illness (a fever most days in the last month; recent unexplained weight loss of 10 lbs or more)
  • Living in a nursing home, on Hospice, or palliative care
  • Non-speaking deafness
  • Non-reliable transportation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

807 participants in 3 patient groups

Standard Acupuncture
Experimental group
Description:
Participants randomized to standard acupuncture will receive 8-15 acupuncture treatments over 3 months.
Treatment:
Procedure: Standard Acupuncture
Enhanced Acupuncture
Experimental group
Description:
Participants randomized to enhanced acupuncture will receive 12-21 acupuncture treatments over 6 months.
Treatment:
Procedure: Enhanced Acupuncture
Usual Care
No Intervention group
Description:
Participants assigned to the usual care arm will not receive acupuncture and will be asked to not get acupuncture over the one-year course of the study.

Trial documents
2

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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