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Effects of Tai Chi on Multisite Pain and Brain Functions in Older Adults

Not Applicable
Completed
Conditions
Chronic Pain
Registration Number
NCT03086772
Lead Sponsor
University of Massachusetts, Boston
Brief Summary

The main purpose of this randomized controlled trial was to assess the feasibility and acceptability of a 12-week Tai Chi program for community-dwelling older adults with chronic multisite pain and a history of falling. In addition, the investigators examined the effects of Tai Chi on pain characteristics, cognition, physical function, gait mobility, levels of pain-related biomarkers, fear of falling and rate of falls in these older adults.

Detailed Description

Older adults aged ≥65 years with multisite pain who reported falling in the past year or current use of an assistive device were recruited from Boston area communities. Participants were randomized to either a Tai Chi (N=28) or a light physical exercise (N=26) program, offered twice weekly for 12 weeks. The primary outcomes were feasibility and acceptability of the 12-week Tai Chi/light exercise program. Secondary outcomes included pain characteristics (pain severity and pain interference), cognition (attention and executive function), physical function (walking speed, strength, and balance), gait mobility (singe-task and dual-task gait), levels of pain-related markers (C-reactive protein, interleukin 6, tumor necrosis factor alpha, and beta endorphin), fear of falling, and rate of falls.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Age of 65 years and older
  • Multisite (2 or more sites) musculoskeletal pain
  • At least one fall in the past year, or currently on an assistive device
  • A sedentary lifestyle
  • Be able to walk 20-feet without personal assistance
  • Be able to communicate in English.
Exclusion Criteria
  • Regular Tai Chi practice
  • Unstable cardiac disease
  • Stroke
  • Rheumatoid arthritis
  • Degenerative neuromuscular disease
  • Parkinson's disease
  • Terminal disease
  • Dementing illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Feasibility and acceptability of the 12-week Tai Chi programOver the 12-week intervention period

Feasibility and acceptability were evaluated by adherence, attendance, optimal program components, and safety.

Secondary Outcome Measures
NameTimeMethod
Gait mobilityBefore and after the 12-week intervention period

Single-task and dual-task gait function was determined by using the PKMAS software and Zeno walkway.

Fear of fallingBefore and after the 12-week intervention period

Fear of falling was measured using the Tinetti Falls Effi- cacy Scale.

Pain characteristicsBefore and after the 12-week intervention period

Pain severity and interference were evaluated by using the Brief Pain Inventory (BPI) questionnaire.

Physical functionBefore and after the 12-week intervention period

Physical function was measured by using the Short Physical Performance Battery (SPPB)

Rate of fallsOver the 12-week intervention and 6 months following the intervention

Rate of falls were recorded by using monthly fall calendars.

CognitionBefore and after the 12-week intervention period

Attention was evaluated by using the Test of Everyday Attention (TEA) questionnaire. Executive function was evaluated by using the Trailmaking A and B tests questionnaire.

Pain-related biomarkersBefore and after the 12-week intervention period

Levels of inflammatory markers and beta endorphin were determined by using biochemistry assays.

Trial Locations

Locations (1)

University of Massachusetts, Boston

🇺🇸

Boston, Massachusetts, United States

University of Massachusetts, Boston
🇺🇸Boston, Massachusetts, United States

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