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Not yet recruiting NCT07595991

Post-osteoporotic Fracture Exercise Program

No phase Interventional Osteoporosis Osteoporotic Fracture

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise Program.
Who it may be relevant to
Registry conditions: Osteoporosis, Osteoporotic Fracture. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Community Osteoporosis Exercise Class for People Post Fracture

Overview

Those with osteoporosis often have weaker bones and this leads to higher chances of fractures. Therefore, the investigators want to evaluate the feasibility and safety of group exercise classes specifically designed for individuals with osteoporosis who had an osteoporotic fracture. By focusing on this high-risk population, the investigators want to see whether such exercise interventions can be an option for improving bone health, reducing the risk of future fractures, and enhancing physical function without compromising safety.

Interventions

  • Other Exercise Program
    Participants complete a 12-week, twice weekly, whole body group exercise program. Participants will also complete qualitative interviews and DXA bone scans.

Primary outcome measures

  • Recruitment Feasibility [Time frame: Assessed over 12 months]
  • Retention Feasibility [Time frame: Assessed at 12 weeks]
  • Exercise Class Adherence [Time frame: Assessed over the 12-week intervention period]
Secondary outcome measures (2)
  • Program Acceptability [Time frame: Assessed at 12 weeks]
  • Intervention Safety [Time frame: Assessed throughout the 12-week intervention period]

Eligibility criteria

Inclusion criteria

  • Diagnosed with osteoporosis.
  • History of low trauma fracture within the past year
  • Cleared for physical activity using the get active questionnaire, 100 bpm resting heart rate or less, 160 mm Hg diastolic blood pressure or less
  • Able to understand and provide informed consent.
  • Residing within the study's geographic area (e.g., London, Ontario).

Exclusion criteria

  • Individuals who do not understand the English language
  • Medical conditions contraindicating participation in exercise (e.g., uncontrolled cardiovascular disease, severe respiratory illness).
  • Cognitive impairments that prevent informed consent or participation.
  • Recent major surgeries or medical events limiting physical activity.
  • Participation in conflicting clinical trials or rehabilitation programs.
  • Residents outside the designated study area.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Canada · 1 center
  • Canadian Centre for Activity and Aging — London

Identifiers

NCT: NCT07595991 · 127410

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗