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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02445664
Other study ID # OP_77
Secondary ID
Status Completed
Phase N/A
First received May 8, 2015
Last updated May 12, 2015
Start date August 2014
Est. completion date November 2014

Study information

Verified date May 2015
Source University of Southern Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The health research ethics committee system
Study type Interventional

Clinical Trial Summary

Osteoporosis is a highly prevalent disease in which non-adherence is a well-recognized problem. Non-adherence may be due to patients´ lack of knowledge, understanding, and involvement. In this study the investigators aimed to determine the effect of an educational video displayed on a tablet-device. The investigators hypothesized that an educational video would increase patients´ knowledge on osteoporosis and treatment at a two week follow up.


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Scheduled for at DXA scan at the osteoporosis clinic

- Currently on once-weekly alendronate treatment

- Informed consent

Exclusion Criteria:

- Patients that do not understand Danish

- Patients having hearing impairments (unable to hear the video)

- Patients having visual impairments (unable to watch the video)

- Patients diagnosed with dementia

- Patients unable to give written informed consent.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Educational video
Video: Information on osteoporosis and alendronate treatment.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Southern Denmark Odense University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Change in knowledge score Baseline and 2-week follow up No
Secondary Change in "confidence to treatment" score, as indicated by participant response to questionnaire. Measured on a scale from 1-10 Baseline and 2-week follow up No
Secondary Change in "satisfaction with the amount of information" score, as indicated by participant response to questionnaire. Measured on a scale from 1-10 Baseline and 2-week follow up No
Secondary Change in "understandability of the information" score, as indicated by participants response to questionnaire. Measured on a scale from 1-10 Baseline and 2-week follow up No
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