Qigong and Exercise Therapy for Low Back Pain in Adults (QEBA)
Primary Purpose
Low Back Pain
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
qigong
exercise therapy
Sponsored by
About this trial
This is an interventional treatment trial for Low Back Pain focused on measuring qigong, traditional chinese medicine, exercise therapy, low back pain
Eligibility Criteria
Inclusion Criteria:
- clinical diagnosis of chronic low back pain since at least 3 months and complaints for a maximum duration of 5 years
- low back pain more prominent than other pain in the spine
- average pain intensity of the last 7 days more or equal to 40 mm measured by a visual analogue scale (VAS 0 - 100 mm)
- intellectual and physical ability to participate in the study
- informed consent
Exclusion Criteria:
- low back pain related to malignancy
- low back pain due to an accident
- inflammatory joint disorders
- previous spine surgery
- protrusion/prolapse of a spinal disk, spondylolisthesis, with radicular symptomatology
- actually doing or planning to do other regular physical exercise during the study with possible positive effects on low back pain - such as swimming, yoga, pilates, tai chi, etc.
- planning to do another therapy during the study with possible positive effects in low back pain, such as physiotherapy, acupuncture, massage, spinal manipulation etc.
- use of pain drugs for other diseases (> 1x/week)
- pregnancy
- severe chronic or acute disease interfering with therapy attendance
- alcohol or substance abuse
- participation in another clinical trial in the last 6 months before study entry
Sites / Locations
- Institute for Social Medicine, Epidemiology, and Health Economics, Charité University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
qigong
exercise therapy
Outcomes
Primary Outcome Measures
average pain intensity during the last 7 days measured on a visual analogue scale (VAS)
Secondary Outcome Measures
disability (Roland-Morris-Questionnaire RMQ)
health related quality of life (SF 36)
credibility of the therapy for patients
patient expectation and self efficacy
therapist's expectation
sleep quality
undesired effects
Full Information
NCT ID
NCT00993980
First Posted
October 13, 2009
Last Updated
July 9, 2012
Sponsor
Charite University, Berlin, Germany
1. Study Identification
Unique Protocol Identification Number
NCT00993980
Brief Title
Qigong and Exercise Therapy for Low Back Pain in Adults
Acronym
QEBA
Official Title
Randomized Multicenter Trial on the Effectiveness of Qigong and a Stabilizing Exercise Therapy in Patients With Low Back Pain
Study Type
Interventional
2. Study Status
Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
January 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charite University, Berlin, Germany
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to assess the effectiveness of qigong for the treatment of low back pain compared to a stabilizing exercise therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
qigong, traditional chinese medicine, exercise therapy, low back pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
127 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
qigong
Arm Title
2
Arm Type
Active Comparator
Arm Description
exercise therapy
Intervention Type
Procedure
Intervention Name(s)
qigong
Intervention Description
one therapy session once a week during three months, that is 12 therapy sessions altogether
Intervention Type
Procedure
Intervention Name(s)
exercise therapy
Intervention Description
one therapy session once a week during three months, that is 12 therapy sessions altogether
Primary Outcome Measure Information:
Title
average pain intensity during the last 7 days measured on a visual analogue scale (VAS)
Time Frame
baseline, 3, 6 and 12 months
Secondary Outcome Measure Information:
Title
disability (Roland-Morris-Questionnaire RMQ)
Time Frame
baseline, 3, 6 and 12 months
Title
health related quality of life (SF 36)
Time Frame
baseline, 3, 6 and 12 months
Title
credibility of the therapy for patients
Time Frame
baseline, 3, 6 and 12 months
Title
patient expectation and self efficacy
Time Frame
baseline, 3, 6 and 12 months
Title
therapist's expectation
Time Frame
baseline, 3, 6 and 12 months
Title
sleep quality
Time Frame
baseline, 3, 6 and 12 months
Title
undesired effects
Time Frame
baseline, 3, 6 and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
clinical diagnosis of chronic low back pain since at least 3 months and complaints for a maximum duration of 5 years
low back pain more prominent than other pain in the spine
average pain intensity of the last 7 days more or equal to 40 mm measured by a visual analogue scale (VAS 0 - 100 mm)
intellectual and physical ability to participate in the study
informed consent
Exclusion Criteria:
low back pain related to malignancy
low back pain due to an accident
inflammatory joint disorders
previous spine surgery
protrusion/prolapse of a spinal disk, spondylolisthesis, with radicular symptomatology
actually doing or planning to do other regular physical exercise during the study with possible positive effects on low back pain - such as swimming, yoga, pilates, tai chi, etc.
planning to do another therapy during the study with possible positive effects in low back pain, such as physiotherapy, acupuncture, massage, spinal manipulation etc.
use of pain drugs for other diseases (> 1x/week)
pregnancy
severe chronic or acute disease interfering with therapy attendance
alcohol or substance abuse
participation in another clinical trial in the last 6 months before study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia M Witt, MD
Organizational Affiliation
Charite University, Berlin, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Social Medicine, Epidemiology, and Health Economics, Charité University Medical Center
City
Berlin
ZIP/Postal Code
10117
Country
Germany
12. IPD Sharing Statement
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Qigong and Exercise Therapy for Low Back Pain in Adults
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