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Chronic Low Back Pain and Primary Health Care

Primary Purpose

Low Back Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Progressive Muscle Relaxation (PMR)
Clinical Massage Therapy (CMT)
Sponsored by
William G Elder JR
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Have a visit with the physician during the 4-week study referral period for that practice
  • Be 21 years of age or older on the date of the visit
  • According to the physician, currently have CLBP
  • Have been a patient in the practice for at least 3 months
  • Have a life expectancy of 6 months or more

Exclusion Criteria:

  • Not have a current or past history of psychosis
  • Not be pregnant

Sites / Locations

  • Department of Family and Community Medicine; University of Kentucky

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Progressive Muscle Relaxation

Clinical Massage Therapy

Arm Description

Outcomes

Primary Outcome Measures

Oswestry Disability Index (ODI)
Survey completed at Baseline, 12 Weeks, and 24 Weeks
Short Form 36 (SF-36)
Health related quality of life survey
Faces Pain Scale - Revised (FPS-R)
Survey

Secondary Outcome Measures

Pain Medication Questionnaire (PMQ) - subset
Survey
Expectations for and Satisfaction with Therapies
Survey
Tampa Scale of Kinesiophobia (TSK) - Subset
Survey
Patient Perceptions of CAM Therapy
Survey
Physician Perceptions of CAM Therapy
Survey
Physician Point-of-Care Card
CLBP visit description and reasons to recommend patients for this therapy study.

Full Information

First Posted
March 30, 2010
Last Updated
June 3, 2014
Sponsor
William G Elder JR
Collaborators
National Institutes of Health (NIH), National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT01147120
Brief Title
Chronic Low Back Pain and Primary Health Care
Official Title
CAM Referral and Outcomes: Chronic Low Back Pain in Urban and Rural Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
June 2014
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
William G Elder JR
Collaborators
National Institutes of Health (NIH), National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Kentucky ranks 2nd in disability among states, with chronic low back pain (CLBP) as a major disability, especially in the investigators rural areas. Kentucky and U.S. health care providers need alternative and effective treatments. Following NCCAM strategic research recommendations, this study will investigate health services outcomes of complementary and alternative medicine (CAM) therapies in an existing primary care practice-based research network (PBRN). The Patients with CLBP are often willing to try therapeutic options outside the conventional medical spectrum. Massage and relaxation therapies have demonstrated fairly good efficacy in controlled trials but their effectiveness in the "real world" of primary care is only beginning to be evaluated. The long-term goal of the proposed project builds on the foundation of these two established therapies to improve treatment of chronic low back pain (CLBP) in primary care practices. Two alternative (CAM) therapies, progressive muscle relaxation (PMR) and clinical massage therapy (CMT), will be studied. The short-term objectives of the proposed project are to: (1) examine outcomes of CAM for patients with CLBP referred from primary care practices, and (2) better understand physician decision-making to recommend CAM therapy for CLBP. Specific Aim 1 will evaluate improvement in health-related outcomes for patients with CLBP when referred to PMR or CMT from primary care. Specific Aim 2 will explore selected factors in primary care physicians' decisions to recommend CAM therapy to these patients. The proposed study is unique in that it addresses "real life" clinical situations and decision-making in both urban and rural clinical practices within an existing PBRN. Should such CAM referral prove successful for ameliorating CLBP, it would provide relatively low cost, non-addictive treatment options for inclusion in the repertoire of primary care physicians.
Detailed Description
The proposed study will investigate health related outcomes of two CAM treatments recommended by primary care physicians for CLBP, and explore selected elements in the decision process to recommend or not recommend one of two CAM treatments. Patients and primary care physicians (PCPs) will participate from metropolitan and nonmetropolitan central Kentucky practices of the Kentucky Ambulatory Network (KAN), Kentucky's statewide primary care practice-based research network (PBRN). Each practice will have a patient participant enrollment period of four weeks. Patients with CLBP who have a visit during the enrollment period in a practice may be eligible to participate in the study, and participating PCPs will be invited to recommend as many eligible patients as they feel comfortable. During patient visits, the PCP may offer a recommendation to the patient to receive PMR or CMT. Patients who agree will be recruited by the KAN/CAM project team staff. Patients who enroll in the CAM recommendation study will receive a 12-week course of PMR or CMT treatments. Outcomes will be measured at three time points: baseline, 12 weeks, and 24 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
138 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Progressive Muscle Relaxation
Arm Type
Active Comparator
Arm Title
Clinical Massage Therapy
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Progressive Muscle Relaxation (PMR)
Intervention Description
Progressive Muscle Relaxation (PMR) will be recorded on PDAs integrated with EMA software and offered to patients who will be instructed in the techniques and PDA use by study coordinators. They will be instructed to practice 25 minutes/day the first two weeks, 35 minutes/day weeks 3 and 4, and 45 minutes/day weeks 5 through 12. These time periods (25/35/45 minute) were selected to allow a more gradual acclimation to PMR.
Intervention Type
Procedure
Intervention Name(s)
Clinical Massage Therapy (CMT)
Intervention Description
PCPs will have the opportunity to refer patients with CLBP to local Licensed Massage Therapists (LMTs) to receive up to 10 clinical massage sessions over a 12-week period. CMT will be provided at no cost to the patients. At their first two sessions, the LMT will evaluate the patient and, with the patient, estimate the number of sessions and determine treatment goals. Based on previous literature, 10 sessions are anticipated over an average 12-week period. However, treatment will vary depending on assessment and progress. At the end of the treatment period, the patients will receive a list of all participating LMTs to facilitate patients' continued or future participation in massage therapy.
Primary Outcome Measure Information:
Title
Oswestry Disability Index (ODI)
Description
Survey completed at Baseline, 12 Weeks, and 24 Weeks
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Title
Short Form 36 (SF-36)
Description
Health related quality of life survey
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Title
Faces Pain Scale - Revised (FPS-R)
Description
Survey
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Secondary Outcome Measure Information:
Title
Pain Medication Questionnaire (PMQ) - subset
Description
Survey
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Title
Expectations for and Satisfaction with Therapies
Description
Survey
Time Frame
Baseline and 12 Weeks
Title
Tampa Scale of Kinesiophobia (TSK) - Subset
Description
Survey
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Title
Patient Perceptions of CAM Therapy
Description
Survey
Time Frame
Baseline, 12 Weeks, and 24 Weeks
Title
Physician Perceptions of CAM Therapy
Description
Survey
Time Frame
Baseline
Title
Physician Point-of-Care Card
Description
CLBP visit description and reasons to recommend patients for this therapy study.
Time Frame
4 weeks per practice (Identify and screen for possible patients)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have a visit with the physician during the 4-week study referral period for that practice Be 21 years of age or older on the date of the visit According to the physician, currently have CLBP Have been a patient in the practice for at least 3 months Have a life expectancy of 6 months or more Exclusion Criteria: Not have a current or past history of psychosis Not be pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William G Elder, PhD
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Family and Community Medicine; University of Kentucky
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40536
Country
United States

12. IPD Sharing Statement

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Chronic Low Back Pain and Primary Health Care

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