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Effects of Modified T'ai Chi on Symptoms in Older Adults With Osteoarthritis

Phase 1
Completed
Conditions
Osteoarthritis
Registration Number
NCT00485043
Lead Sponsor
University of Kansas
Brief Summary

The purpose of this study was to evaluate the effects of TC for Arthritis on physical function, pain, and stiffness in older adults with knee/hip OA. Two hypotheses were tested:

1. Individuals in the TC group will demonstrate greater improvements in physical function compared to control group participants.

2. Individuals in the TC group will demonstrate greater decreases in pain and stiffness compared to control group participants.

Detailed Description

Exercise is considered a vital component of osteoarthritis (OA) treatment. T'ai Chi (TC) is a unique exercise intervention with low-velocity movements. Few studies have addressed the effects of TC on arthritis symptoms and function. TC for Arthritis was modified specifically for people with OA and consists of a standardized set of forms.

The purpose of this study was to evaluate the effectiveness of a low-dose TC for Arthritis on physical function, pain, and stiffness in individuals with OA.

Twenty-seven older adults with OA (mean age-81.3 years) completed an 8 week non-randomized controlled pre-post test quasi-experimental design study of TC for Arthritis. Physical function, pain, and stiffness were measured at baseline and 8 weeks for the TC and control groups using the WOMAC™ 3.1 Index. Qualitative data from interviews and participant observations were analyzed in order to understand the participants' expectations and experiences with TC.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Ability to walk independently,
  • Speak and understand English,
  • Understand the consent process; and
  • Give informed consent.
Exclusion Criteria
  • Participation in rehabilitation or another TC class,
  • At the time of recruitment; and
  • Inability to confirm medical stability for safe participation with healthcare provider.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
physical function8 weeks
Secondary Outcome Measures
NameTimeMethod
pain and stiffness8 weeks
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