Veterans Response to Dosage in Chiropractic Therapy

NCT04087291 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 766

Last updated 2025-09-16

No results posted yet for this study

Summary

This study evaluates how Veterans with chronic low back pain (cLBP) respond to varying doses of chiropractic therapy and how health services utilization are impacted as a result.

There are 2 phases in this study. In Phase 1, half of participants will receive a low dose (1-5 visits) of chiropractic care for 10 weeks, while the other half will receive a higher dose (8-12 visits) for 10 weeks. At the end of Phase 1, participants in each group will be randomized again to receive either chronic chiropractic pain management (CCPM) (1 scheduled chiropractic visit per month x 10 months) or no CCPM for 10 months.

Conditions

  • Low Back Pain
  • Patient Acceptance of Health Care
  • Veterans Health

Interventions

OTHER

Chiropractic Care

Chiropractic interventions: 1. Patient education. 2. Passive interventions, such as spinal manipulation and myofascial therapies which include thrust type (high velocity-low amplitude) spinal manipulation for the low back, non-thrust manipulation (joint mobilization), and use of manually held instruments, such as an Activator. Myofascial therapies are also commonly used, such as myofascial release and trigger point therapy. 3. Transitional interventions, such as therapeutic exercise. 4. Recommendations for active interventions, such as general exercise and mind-body therapies. 5. Self-management advice, which refers to advice given to build the capacity of a person to self-monitor, control, and/or reduce the impact of a condition over time.

Sponsors & Collaborators

  • Yale University

    collaborator OTHER
  • University of Iowa

    collaborator OTHER
  • Dartmouth College

    collaborator OTHER
  • VA Connecticut Healthcare System

    collaborator FED
  • Minneapolis Veterans Affairs Medical Center

    collaborator FED
  • Iowa City VA Health Care System

    collaborator FED
  • VA Greater Los Angeles Healthcare System

    collaborator FED
  • Office of Research on Women's Health (ORWH)

    collaborator NIH
  • National Center for Complementary and Integrative Health (NCCIH)

    collaborator NIH
  • Duke University

    collaborator OTHER
  • Palmer College of Chiropractic

    lead OTHER

Principal Investigators

  • Christine Goertz, DC, PhD · Duke University

  • Cynthia Long, PhD · Palmer Center for Chiropractic Research (PCCR)

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-22
Primary Completion
2025-05-20
Completion
2025-05-20

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04087291 on ClinicalTrials.gov