Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00993980
Other study ID # QEBA-09
Secondary ID
Status Completed
Phase N/A
First received October 13, 2009
Last updated July 9, 2012
Start date October 2009
Est. completion date January 2011

Study information

Verified date July 2012
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 127
Est. completion date January 2011
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 60 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
qigong
one therapy session once a week during three months, that is 12 therapy sessions altogether
exercise therapy
one therapy session once a week during three months, that is 12 therapy sessions altogether

Locations

Country Name City State
Germany Institute for Social Medicine, Epidemiology, and Health Economics, Charité University Medical Center Berlin

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary average pain intensity during the last 7 days measured on a visual analogue scale (VAS) baseline, 3, 6 and 12 months No
Secondary disability (Roland-Morris-Questionnaire RMQ) baseline, 3, 6 and 12 months No
Secondary health related quality of life (SF 36) baseline, 3, 6 and 12 months No
Secondary credibility of the therapy for patients baseline, 3, 6 and 12 months No
Secondary patient expectation and self efficacy baseline, 3, 6 and 12 months No
Secondary therapist's expectation baseline, 3, 6 and 12 months No
Secondary sleep quality baseline, 3, 6 and 12 months No
Secondary undesired effects baseline, 3, 6 and 12 months Yes
See also
  Status Clinical Trial Phase
Completed NCT03916705 - Thoraco-Lumbar Fascia Mobility N/A
Completed NCT04007302 - Modification of the Activity of the Prefrontal Cortex by Virtual Distraction in the Lumbago N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Recruiting NCT03600207 - The Effect of Diaphragm Muscle Training on Chronic Low Back Pain N/A
Completed NCT04284982 - Periodized Resistance Training for Persistent Non-specific Low Back Pain N/A
Recruiting NCT05600543 - Evaluation of the Effect of Lumbar Belt on Spinal Mobility in Subjects With and Without Low Back Pain N/A
Withdrawn NCT05410366 - Safe Harbors in Emergency Medicine, Specific Aim 3
Completed NCT03673436 - Effect of Lumbar Spinal Fusion Predicted by Physiotherapists
Completed NCT02546466 - Effects of Functional Taping on Static Postural Control in Patients With Non-specific Chronic Low Back Pain N/A
Completed NCT00983385 - Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking Either WHO Step I or Step II Analgesics or no Regular Analgesics Phase 3
Recruiting NCT05156242 - Corticospinal and Motor Behavior Responses After Physical Therapy Intervention in Patients With Chronic Low Back Pain. N/A
Recruiting NCT04673773 - MY RELIEF- Evidence Based Information to Support People Aged 55+ Years Living and Working With Persistent Low-back Pain. N/A
Completed NCT06049277 - Mulligan Technique Versus McKenzie Extension Exercise Chronic Unilateral Radicular Low Back Pain N/A
Completed NCT06049251 - ELDOA Technique Versus Lumbar SNAGS With Motor Control Exercises N/A
Completed NCT04980469 - A Study to Explore the Effect of Vitex Negundo and Zingiber Officinale on Non-specific Chronic Low Back Pain Due to Sedentary Lifestyle N/A
Completed NCT04055545 - High Intensity Interval Training VS Moderate Intensity Continuous Training in Chronic Low Back Pain Subjects N/A
Recruiting NCT05944354 - Wearable Spine Health System for Military Readiness
Recruiting NCT05552248 - Assessment of the Safety and Performance of a Lumbar Belt
Completed NCT05801588 - Participating in T'ai Chi to Reduce Back Pain and Improve Quality of Life N/A
Completed NCT05811143 - Examining the Effects of Dorsal Column Stimulation on Pain From Lumbar Spinal Stenosis Related to Epidural Lipomatosis.