Provincial Roll-Out Bone Health Strategy
Primary Purpose
Osteoporosis
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Resistance training
Sponsored by
About this trial
This is an interventional treatment trial for Osteoporosis focused on measuring Exercise, Resistance training
Eligibility Criteria
Inclusion Criteria:
- inactive (less than twice weekly exercising) women aged 65-75 years old
Sites / Locations
Outcomes
Primary Outcome Measures
Physiologic Profile Assessment (Fall Risk)
Secondary Outcome Measures
Bone strength using peripheral quantitative computed tomography (pQCT)
Full Information
NCT ID
NCT00431002
First Posted
January 31, 2007
Last Updated
May 13, 2017
Sponsor
University of British Columbia
1. Study Identification
Unique Protocol Identification Number
NCT00431002
Brief Title
Provincial Roll-Out Bone Health Strategy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Withdrawn
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2008 (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main purpose of this study is to investigate the effect of two different group-based exercise programs on fall risk (muscular strength and balance) and bone strength in older women aged over 65-75 years who have low bone mass. We are also trying to determine if once a week exercise is as effective on health outcomes as twice a week. We hypothesize that twice a week exercise will be more effective than once a week or sham exercise.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
Exercise, Resistance training
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Resistance training
Intervention Description
See Detailed Description.
Primary Outcome Measure Information:
Title
Physiologic Profile Assessment (Fall Risk)
Secondary Outcome Measure Information:
Title
Bone strength using peripheral quantitative computed tomography (pQCT)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
inactive (less than twice weekly exercising) women aged 65-75 years old
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
K M Khan, PhD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Provincial Roll-Out Bone Health Strategy
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