- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02445664
Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment
May 12, 2015 updated by: Kirsa Skov, University of Southern Denmark
Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment - a Randomized, Controlled Trial
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.
Study Overview
Study Type
Interventional
Enrollment (Actual)
67
Phase
- Not Applicable
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 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
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Video intervention
A tablet-administered educational video (10 minutes duration).
|
Video: Information on osteoporosis and alendronate treatment.
|
No Intervention: Control
No intervention (no video)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in knowledge score
Time Frame: Baseline and 2-week follow up
|
Baseline and 2-week follow up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in "confidence to treatment" score, as indicated by participant response to questionnaire.
Time Frame: Baseline and 2-week follow up
|
Measured on a scale from 1-10
|
Baseline and 2-week follow up
|
Change in "satisfaction with the amount of information" score, as indicated by participant response to questionnaire.
Time Frame: Baseline and 2-week follow up
|
Measured on a scale from 1-10
|
Baseline and 2-week follow up
|
Change in "understandability of the information" score, as indicated by participants response to questionnaire.
Time Frame: Baseline and 2-week follow up
|
Measured on a scale from 1-10
|
Baseline and 2-week follow up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
August 1, 2014
Primary Completion (Actual)
November 1, 2014
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
May 8, 2015
First Submitted That Met QC Criteria
May 12, 2015
First Posted (Estimate)
May 15, 2015
Study Record Updates
Last Update Posted (Estimate)
May 15, 2015
Last Update Submitted That Met QC Criteria
May 12, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- OP_77
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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