Aging
Conditions
Brief summary
The investigators propose to test the effects of an 8-week supervised, site-based, group yoga intervention on cognition and functional fitness in older adults. The SAY Exercise study will compare the yoga group to a stretching group to determine if the program improves attention and cognition, reduces functional limitations, enhances functional performance in everyday activities, as well as psychological health in sedentary older adults between 55-80 years of age. The investigators also propose to assess heart rate variability using a 3-lead EKG and salivary cortisol levels to understand the moderators of the yoga-cognition relationship.
Interventions
BEHAVIORALYoga Condition
Classes lasting one hour, held 3 times per week for 8 weeks.
BEHAVIORALStretching Condition
Classes lasting one hour, held 3 times per week for 8 weeks.
Sponsors
University of Illinois at Urbana-Champaign
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
55 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
* 55-80 yrs of age * Low active: zero to two days of physical activity (\>30 minutes per day) per week, in previous six months * Personal physicians consent to participate in testing and exercise intervention * Not involved in any other physical activity/exercise research study or cognitive training study. * Adequate responses to the Telephone interview of Cognitive Status (TICS-M) questionnaire * Corrected (near and far) acuity of 20/40 or better in both eyes * Initial depression score on GDS-15 below clinical levels (\>5) * Able to get up and down from the floor * Comfortable with reading, writing and speaking English
Exclusion criteria
* Below 55 or over 80 years of age * High physical activity levels (more than 2 times per week, \>30 minutes, in the last 6 months) * Regular yoga practitioners (previously or currently practicing for more than 6 months) * Involved in other physical activity/exercise research study or cognitive training study * Non-consent of the physician * Inadequate response on the GDS-15 and TICS-M * Uncorrected (near and far) acuity of greater than 20/40 in either eye * Inability to communicate effectively in English * Intent to be away from the area for a long period of time resulting in more than 2 absences at the exercise sessions
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in cognition as assessed by a neuropsychological battery of computer based and paper pencil tests from baseline to 8 weeks | Baseline - 8 week | Participants will complete a neuropsychological battery of tasks assessing memory, attention, decision making at baseline (before beginning the program) and at week 8 (after completing the exercise program). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in functional fitness from baseline to 8 weeks | Baseline - 8 week | Participants will complete a battery of physical function tests assessing balance, flexibility, strength and mobility at baseline and week 8. |
| Change in psychosocial outcomes from baseline to 8 weeks | Baseline - 8 week | Participants will complete a packet of questionnaires assessing self-esteem, postitive and negative affect including anxiety and depression, self-efficacy and other psychosocial outcomes. |
| Change in salivary cortisol from baseline to 8 weeks | Baseline - week 8 | Participants will be providing a small saliva sample via a passive drool into a vial. The compound of interest is cortisol (an indicator of body stress). |
| Change in heart rate variability from baseline to 8-weeks | Baseline - 8 week | The EKG for each participant will also be recorded in response to a 5 minute unpaced (normal) breathing and 5-minute paced (set to a metronome) breathing. All participants will complete these assessments at baseline and week 8. |
Countries
United States
Outcome results
None listed