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CompletedNCT01203657Updated Aug 19, 2016

UCLA Tai Chi in a Community Setting Study

An interventional study of Tai Chi in Physical Activity and Fatigue, sponsored by University of California, Los Angeles. Completed at 1 site in United States. Open to participants aged 60 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-08-19.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
47
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

Although a number of studies have examined the effects of Tai Chi in older adult populations, few have methodically assessed its effects on vitality, fatigue and physical activity. Some studies have shown that fatigue relates to negative mood and poor health-related quality of life in older persons.

Tai Chi is an ancient Chinese form of calisthenics that utilizes the body's internal energy (chi), mind, and breathing; which may be a useful exercise for older adults in increasing their activity level. A twenty-four of Yang style of Tai Chi is a simple form of Tai Chi that is particularly well-suited for older adults. This proposed study to investigate the effects of a Tai Chi intervention on decreasing fatigue level, and increasing level of activity in healthy older adults.

The investigators research group has focused on the Tai Chi as a strategy to reduce stress and improve sleep, and their preliminary evidence suggest it strongly affects energy level and vitality. The investigators are focused on taking this intervention into the community testing its efficacy. The investigators preliminary data shows that Tai Chi is of benefit to older adults; however, this study will test whether their research findings are generalizable to community settings.

Tai Chi-naïve participants from Culver City Senior Center will receive a 10-week Tai Chi. The investigators will compare this group to a wait-list control group. All subjects will receive a packet of questionnaires of pre- and post-intervention vitality, fatigue and health-related quality of life. Subjects will also be given an activity monitor to wear for 2 days before they start the Tai Chi class and for 2 days after they complete the class, to determine if there is a change in general physical activity level.

02

Conditions studied

  • Physical Activity
  • Fatigue

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Keywords

  • exercise
  • physical activity
  • tai chi
03

In context

Fatigue

1,860 studies on the registry are indexed under Fatigue; 376 are open to participants now.

This study's enrollment of 47 is below the median of 54 across 1,440 interventional studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.

Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy
  • Older adult > 60 years of age

Exclusion criteria

Exclusion Criteria:

  • Older adults who have severe osteoarthritis or chronic pain disorders
  • Non ambulatory
  • Any condition that would adversely impact their participation in Tai Chi
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
47 participants (actual)

Study arms

  • Experimental
    Tai Chi

    Tai Chi instruction, 2x week in a community senior center setting

    Behavioral: Tai Chi

  • No intervention
    Wait List Control

    This is a wait list control group. There is no active or placebo intervention.

Interventions

  • BehavioralTai Chi

    Tai Chi classes, 60 minutes, 2x week

    Also known as: exercise, relaxation

06

What researchers measure

Primary outcomes

  1. Physical Activity

    Objectively assessed physical activity measured using accelerometers

    Time frame: Immediately post-intervention (10 weeks)

Secondary outcomes

  1. Vitality

    Measures of fatigue, mood, perceived stress and vitality, administered via self-report

    Time frame: Immediately post-intervention (10 weeks)

07

Study locations

1 site
  • UCLA
    Los Angeles, California 90095, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 19, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01203657
Lead sponsor
University of California, Los Angeles
Responsible party
Sponsor
First posted
Sep 16, 2010
Start date
Jan 2010
Primary completion
Jan 2011
Completion
Jan 2011
Last update
Aug 19, 2016

Study contacts

Sarosh Motivala, Ph.D.
principal investigator · University of California, Los Angeles

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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