Qigong and Exercise for Neck Pain in Adults (QENA)
Not Applicable
Completed
- Conditions
- Chronic Neck Pain
- Interventions
- Procedure: exercise therapyProcedure: Qigong
- Registration Number
- NCT00615732
- Lead Sponsor
- Charite University, Berlin, Germany
- Brief Summary
The purpose of this study is to assess the effectiveness of qigong for the treatment of chronic neck pain compared to exercise therapy and waiting list group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 123
Inclusion Criteria
- clinical diagnosis of chronic neck pain since at least 6 months and complaints for a maximum duration of 5 years
- neck 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)
- normal mobility of the cervical spine
- intellectual and physical ability to participate in the study
- informed consent
Exclusion Criteria
- cervical pain related to malignancy
- cervical 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 neck pain - such as swimming, yoga, pilates, tai chi, 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
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 2 exercise therapy exercise therapy 1 Qigong qigong
- Primary Outcome Measures
Name Time Method average pain intensity during the last 7 days measured on a visual analogue scale (VAS) baseline, 3, 6, 12, and 24 months
- Secondary Outcome Measures
Name Time Method Neck Pain and Disability Scale (NPAD, Wheeler 1999) baseline, 3, 6, 12, and 24 months health related quality of life (SF-36) baseline, 3, 6, 12 and 24 months patient expectation and self efficacy (questionnaire) Baseline, 3, 6, 12, and 24 months therapist's expectation baseline, 3, 6, 12, and 24 months undesired effects 3, 6, 12, and 24 months semi-structured interviews to detect changes due to therapy and to assess the used questionnaires 3 and 6 months
Trial Locations
- Locations (1)
Institute for Social Medicine, Epidemiology, and Health Economics, Charité University Medical Center
🇩🇪Berlin, Germany