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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00464412
Other study ID # 1-Kasper
Secondary ID
Status Completed
Phase Phase 1
First received April 19, 2007
Last updated May 8, 2007
Start date January 2006
Est. completion date February 2006

Study information

Verified date May 2007
Source Valdosta State University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date February 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Behavioral:
Education


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Valdosta State University Roanoke College

Outcome

Type Measure Description Time frame Safety issue
Primary Osteoporosis Knowledge 7 days and 21 days post educational intervention
Primary Osteoporosis Beliefs 7 days and 21 days post educational intervention
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