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Osteo-cise: Strong Bones for Life. An Inclusive Evidence-based Multi-component Exercise, Falls Prevention and Osteoporosis Education Program.

Effectiveness and feasibility of a multi-site, multi-faceted exercise intervention combined with an osteoporosis education program on bone mineral density, muscle function and quality of life in community dwelling older adults at risk of osteoporosis.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000100291
Enrollment
180
Registered
2009-02-13
Start date
2009-07-01
Completion date
2009-11-17
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Osteoporosis and low trauma fractures currently affect 2.2 million Australians, which is projected to rise to three million people by 2021, with a fracture occurring every 3½ minutes. Currently the medical paradigm of ‘cure’ for osteoporosis is less than ideal because the limited pharmacological agents available are directed to those who already have the disease or are at increased risk. A more effective approach to reduce the burden of this disease is prevention at the population level. That is, defining models that are efficacious, safe, and can be implemented to a large cross-section of the community. Exercise fulfils most of these criteria, with the added advantage of having beneficial effects on multiple health outcomes. The aim of this 18 month RCT is to evaluate the feasibility and effectiveness of a community-based exercise (high velocity resistance and weight-bearing exercise) and osteoporosis education/awareness program for optimising musculoskeletal health and function and general well-being in older Australians at increased risk of osteoporosis and fractures.

Interventions

An 18 month randomised controlled trial (12 month intervention with 6 month follow-up) consisting of a multi-component exercise program involving resistance (strength) and power training, balance and mobility activities (60 minutes, 3 times per week for 12 months) combined with osteoporosis education sessions. These interactive education sessions (~60 minutes) will be held every 3 months (4 sessions over 12 months) at a local community/recreation centre and will include information (presentation

An 18 month randomised controlled trial (12 month intervention with 6 month follow-up) consisting of a multi-component exercise program involving resistance (strength) and power training, balance and mobility activities (60 minutes, 3 times per week for 12 months) combined with osteoporosis education sessions. These interactive education sessions (~60 minutes) will be held every 3 months (4 sessions over 12 months) at a local community/recreation centre and will include information (presentation and handout material) related to: risk factors for osteoporosis; best practice exercise and nutrition guidelines; understanding bone density results; strategies to reduce the risk of falling; communicating clearly with your doctor, and medications for the treatment of osteoporosis. All participants will receive daily calcium (700 mg) and vitamin D (1200 IU) supplements. Follow-up testing will be conducted 6 months after the intervention to assess any residual benefits.

Sponsors

The University of Melbourne
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

Osteopenia in the hip (Femoral neck or total hip BMD T-score: -1.0 to -2.5 SD)

Exclusion criteria

Current or prior (6 months) participation in resistance training or a structured weight-bearing exercise program, acute or terminal illness, moderate or severe cognitive impairment (inability to understand and provide written informed consent and/or follow instructions), unstable or ongoing cardiovascular/respiratory disorders, musculoskeletal or neurological disease disrupting voluntary movement or that might limit training, upper or lower extremity fracture in the past 3 months, unwillingness to be randomised to one of the two groups or complete the study requirements.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 26, 2026