- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00464412
The Effect of a Short Educational Program on Young Women's Knowledge and Beliefs About Osteoporosis
May 8, 2007 updated by: Valdosta State University
The purpose of the study is to determine the effect of a short educational program on young women's knowledge and beliefs about osteoporosis.
They hypothesis is that following the intervention women who receive the educational program will have greater knowledge and beliefs about osteoporosis.
Study Overview
Detailed Description
Objective.
To determine the effect of a short osteoporosis educational program on young women's knowledge and beliefs about osteoporosis.
Methods.
Ten college physical activity classes enrolling 133 predominantly Caucasian women (age range 18 to 21 years) were randomized to an osteoporosis educational program or control.
Knowledge and beliefs about osteoporosis were assessed at baseline and at one week and three weeks following the intervention using the Multiple Osteoporosis Prevention Survey.
Knowledge was defined as the ability to identify correctly osteoporosis risk factors.
Beliefs were measured with the use of a five point Likert type scale.
The educational program was comprised of a lecture and printed materials developed by the National Osteoporosis Foundation.
Chi-square and analysis of variance evaluated for between group differences.
Alpha was set at 0.05.
Study Type
Interventional
Enrollment (Actual)
135
Phase
- Phase 1
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Women enrolled in a mid-atlantic college physical activity course
Exclusion Criteria:
- Unable to partake in three survey's and one educational lesson
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Osteoporosis Knowledge
Time Frame: 7 days and 21 days post educational intervention
|
7 days and 21 days post educational intervention
|
Osteoporosis Beliefs
Time Frame: 7 days and 21 days post educational intervention
|
7 days and 21 days post educational intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mark J Kasper, EdD, Valdosta State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2006
Study Completion (Actual)
February 1, 2006
Study Registration Dates
First Submitted
April 19, 2007
First Submitted That Met QC Criteria
April 19, 2007
First Posted (Estimate)
April 23, 2007
Study Record Updates
Last Update Posted (Estimate)
May 9, 2007
Last Update Submitted That Met QC Criteria
May 8, 2007
Last Verified
May 1, 2007
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1-Kasper
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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