Tai Chi Mind-Body Therapy for Fibromyalgia
Recruitment status was Active, not recruiting
| Tracking Information | |||||
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| First Received Date ICMJE | August 9, 2007 | ||||
| Last Updated Date | December 16, 2009 | ||||
| Start Date ICMJE | June 2007 | ||||
| Estimated Primary Completion Date | May 2009 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Fibromyalgia Impact Questionnaire score [ Time Frame: wks 12 and 24 ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE |
Fibromyalgia Impact Questionnaire score | ||||
| Change History | Complete list of historical versions of study NCT00515008 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
Tender Point Count, Fibromyalgia Intensity Score, Physicians' Assessments of Fibromyalgia Severity, Sleep Quality, Depression Index, Physical Performance, Self-Efficacy and Health Related Quality of Life [ Time Frame: Wks 12 and 24 ] [ Designated as safety issue: No ] | ||||
| Original Secondary Outcome Measures ICMJE |
Tender Point Count, Fibromyalgia Intensity Score, Physicians' Assessments of Fibromyalgia Severity, Sleep Quality, Depression Index, Physical Performance, Self-Efficacy and Health Related Quality of Life | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Tai Chi Mind-Body Therapy for Fibromyalgia | ||||
| Official Title ICMJE | Tai Chi Mind-Body Therapy for Fibromyalgia: a Pilot Single-Blind Randomized Controlled Trial. | ||||
| Brief Summary | The purpose of this study is to obtain preliminary data on the effects of Tai Chi on musculoskeletal pain, fatigue, sleep quality, psychological distress, physical performance,and health status in 60 patients with fibromyalgia. |
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| Detailed Description | Fibromyalgia (FM) is a common, complex chronic condition marked by diffuse musculoskeletal pain, fatigue, functional impairment, disability, and psychological distress that affects 6-10 million people in the United States (US). There are currently no satisfactory pharmacological or non-pharmacological treatments for FM. New cost-effective strategies that reduce musculoskeletal pain and improve emotional and physical functioning as well as quality of life in people with FM are urgently needed. Tai Chi is a traditional Chinese discipline with both physical and mental components that appears to benefit a variety of chronic conditions. The physical component provides exercise that is consistent with that recommended for FM (muscle conditioning and aerobic cardiovascular exercise), while the mental component has the potential to improve psychological well-being. These effects are especially pertinent for the treatment of individuals with FM. This is a pilot randomized controlled trial of Tai Chi for fibromyalgia. We plan to enroll 60 patients with fibromyalgia over a two year period. Participants are randomized to either a Tai Chi program or an attention control intervention. Assessments are performed at baseline, week 12 and week 24. This study will provide preliminary data on the potential acceptability and safety of Tai Chi for FM and will help guide the design of a future large-scale study of the efficacy of this alternative therapy. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
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| Condition ICMJE | Fibromyalgia | ||||
| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Active, not recruiting | ||||
| Estimated Enrollment ICMJE | 60 | ||||
| Estimated Completion Date | May 2009 | ||||
| Estimated Primary Completion Date | May 2009 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria
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| Gender | Both | ||||
| Ages | 21 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00515008 | ||||
| Other Study ID Numbers ICMJE | R21 AT003621, R21AT003621 | ||||
| Has Data Monitoring Committee | Yes | ||||
| Responsible Party | Chenchen Wang, Principal Investigator, New England Medical Center Hospitals, Inc. Dept of Medicine | ||||
| Study Sponsor ICMJE | Tufts Medical Center | ||||
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| Investigators ICMJE |
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| Information Provided By | Tufts Medical Center | ||||
| Verification Date | December 2009 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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