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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00227071
Other study ID # BMC 1999-65
Secondary ID
Status Completed
Phase N/A
First received September 23, 2005
Last updated January 3, 2006
Start date September 1999
Est. completion date June 2002

Study information

Verified date September 2005
Source University of Saskatchewan
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

Compare the effect of aquatic,land and no exercise on fall risk factors in women diagnosed with osteoporosis


Description:

Background and Purpose: Fall prevention through exercise is an ongoing goal of researchers and clinicians. This study compared the effects of aquatic exercise (AE), land exercise (LE) and no exercise (NE) on fall risk factors. Subjects: Seventy-three women, 60 or older, with osteoporosis (OP). Method: Randomized clinical trial comparing balance, posture, strength, mobility, function, falls, and quality of life. Results: Significant differences (p<0.05) were found for participants’ ratings of global change (AE and LE > NE), tandem balance (AE > LE) and function (LE > AE). Joint pain and falls occurred more often during LE. Discussion and Conclusion: Participants experienced significant global improvement with both AE and LE. Less joint pain, reduced falls and improved balance were found in AE, however LE was more effective in improving functional ability at home. Clinicians should consider the individual’s specific impairments and risk factors when recommending exercise programs on land or in water.


Recruitment information / eligibility

Status Completed
Enrollment 73
Est. completion date June 2002
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 60 Years and older
Eligibility Inclusion Criteria:

- age 60 or older

- diagnosed with osteoporosis

- female

Exclusion Criteria:

- has not been involved in regular exercise in past 2 months

- does not have any medical or neurological condition that would significantly limit activities of daily living, such that involvement in an exercise program would jeopardize safety

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
exercise


Locations

Country Name City State
Canada School of Physical Therapy Saskatoon Saskatchewan

Sponsors (2)

Lead Sponsor Collaborator
University of Saskatchewan Saskatchewan Health Research Foundation

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary muscle strength
Primary balance
Primary mobility
Primary function
Primary quality of life
Secondary bone status
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