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Trial registered on ANZCTR
Registration number
ACTRN12607000472471
Ethics application status
Approved
Date submitted
14/08/2007
Date registered
19/09/2007
Date last updated
27/04/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
Progressive Load Training for the Quadriceps Muscle Associated to Proprioception Exercises for the Prevention of Falls in Postmenopausal Women with Osteoporosis: a randomized controlled trial
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Scientific title
Eighteen weeks of Progressive Load Training for the Quadriceps Muscle Associated to Proprioception Exercises for the Prevention of Falls in Postmenopausal Women with Osteoporosis: a randomized controlled trial
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
postmenopausal women with osteoporosis
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Condition category
Condition code
Physical Medicine / Rehabilitation
2343
2343
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0
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Physiotherapy
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Musculoskeletal
2407
2407
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0
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Osteoporosis
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention 2 times a week for 18 weeks, 50 patients per group Group 1: exercises of proprioception, balance (Balance was realized in dynamic and static for a period of 30min, Walking on the tips of the toes and the heel, walking sideways, walking for a while with leg contra-lateral arm, standing on one leg, and standing in the tandem position, with gradually increasing the period of permanence in these last two static position. Elastic Jump), and muscular strength (exercisers to the extension muscles of the knee) and stretching exercisers. group 2: control group
Both groups receive treatment clinical (medication) for osteoporosis.
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Intervention code [1]
2028
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Rehabilitation
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Comparator / control treatment
placebo:after 18 weeks - education about devices that prevent falls
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Function,
Timed up and go test,
Berg Balance Scale,
1RM (one repetition maximum) quadriceps muscle
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Assessment method [1]
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Timepoint [1]
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An initial assessment on first week and a last assessment after 18 weeks and 6 weeks follow-up
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Secondary outcome [1]
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Short Form - 36,
Number of falls
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Assessment method [1]
5406
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Timepoint [1]
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An initial assessment on first week and a last assessment after 18 weeks and 6 weeks follow-up
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Eligibility
Key inclusion criteria
Inclusion: Females, ages varying from 55-75, bone mineral density with a T-score below – 2.5 of standard deviation in the spine or femur according to the criteria established by WHO (World Health Organization), with no regular physical exercise practice three months before.
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Minimum age
55
Years
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Maximum age
75
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Exclusion: severe visual deficiency, severe hearing impairment, important vestibular changes, use of assistive gait devices (orthosis and or prosthesis), absolute contraindications for the practice of physical exercises according to the American College of Sports Medicine, other diseases that may affect muscular strength, balance or flexibility and the use of medications prescribed for the reduction of balance.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/02/2007
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Brazil
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State/province [1]
562
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Funding & Sponsors
Funding source category [1]
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Other
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Name [1]
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Federal University of Sao Paulo and
Ambulatory of Specialities of Grajau - University of Santo Amaro
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Address [1]
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Rua Pedro de Toledo 598
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Country [1]
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Brazil
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Primary sponsor type
University
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Name
Lucas Emmanuel Pedro de Paiva Teixeira
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Address
Rua Pedro de Toledo 598
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Country
Brazil
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Secondary sponsor category [1]
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University
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Name [1]
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Virginia Fernandes Moca trevisani
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Address [1]
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Rua Pedro de Toledo 598
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Country [1]
2272
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Brazil
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Ethics Committee - Federal University of Sao Paulo
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Ethics committee address [1]
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Rua Botucatu 572
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Ethics committee country [1]
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Brazil
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Date submitted for ethics approval [1]
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12/12/2006
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Approval date [1]
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12/01/2007
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Ethics approval number [1]
4410
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ID: CEP 1910/06
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Summary
Brief summary
Objective of the study: to verify the efficiency of the balance training, proprioception, and muscle strength exercises concerning the improvement of the functional capacity and quality of life of women with osteoporosis, through validated questionnaires and functional tests. Hypothesis: Proprioception, balance and muscle strength trainings are effective in the falls prevention and reduction of its risk factors, improving the quality of life and functional capacity of patients with osteoporosis, through the acceleration of their motor responses, improving therefore the performance of their daily life activities.
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Trial website
www.unifesp.br
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Lucas Emmanuel Pedro de Paiva Teixeira
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Address
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Rua Pedro de Toledo 598
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Country
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Brazil
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Phone
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55-11-76810702
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Virgínia Fernandes Moça Trevisani
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Address
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Rua Pedro de Toledo 598
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Country
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Brazil
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Phone
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55-11-55752970
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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