Mode
Text Size
Log in / Sign up
N/A N=36 Randomized Single-blind Other

Yoga for Managing Knee Osteoarthritis in Older Women: a Feasibility Study

Osteoarthritis, Knee · Quality of Life · Poor Quality Sleep · Physical Impairment

Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Mar 2014
Primary outcome: Primary: Absolute Value of OA Symptoms at 8 Weeks — 39.3; 31.0 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Hatha yoga (Behavioral)
Age
Older Adult · 65+ yrs
Sex
Female
Sponsor
University of Minnesota
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Absolute Value of OA Symptoms at 8 Weeks
39.3; 31.0
PRIMARY
Absolute Value of OA Pain at 8 Weeks
1; 1
SECONDARY
Absolute Value of Physical Performance of the Lower Extremities (LE) at 8 Weeks
9.0; 10.0
SECONDARY
Absolute Value of Quality of Sleep at 8 Weeks
6.1; 5.0
SECONDARY
Absolute Value of Quality of Life at 8 Weeks
51.7; 49.7; 38.7; 38.0; 7.7; 7.5
SECONDARY
Absolute Value of BMI at 8 Weeks
28.9; 28.7

Summary

The study hypothesized that it is feasible and safe to use Hatha yoga in older women with knee osteoarthritis (OA), and practicing Hatha yoga regularly will help reduce pain and stiffness, enhance physical function, and improve quality of sleep and quality of life in older women with knee OA.

Eligibility Criteria

Inclusion Criteria

  • community-dwelling women aged 65 years or over
  • had a symptomatic OA of knee diagnosis for at least 6 months
  • had no previous training in any form of yoga; and
  • were not currently participating in a supervised exercise program
  • cognitively intact

Exclusion Criteria

  • symptoms of joint locking;
  • instability indicated by chronic use of a knee brace, cane, walker, or wheelchair;
  • a corticosteroid injection in the symptomatic joint within three months of study entry;
  • a hyaluronic acid injection in the symptomatic joint within six months of study entry;
  • a history of knee surgery within the last two years or a joint replacement at any point;
  • individuals who had self-reported significant medical comorbidities that might preclude exercise participation such as: a) uncontrolled high blood pressure or existing heart condition; and b) other comorbid condition with overlapping symptoms (i.e. fibromyalgia, rheumatoid arthritis) were also be excluded.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01832155). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search