Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment
Primary Purpose
Osteoporosis
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Educational video
Sponsored by
About this trial
This is an interventional health services research trial for Osteoporosis focused on measuring Patient education, Video intervention
Eligibility Criteria
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.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Video intervention
Control
Arm Description
A tablet-administered educational video (10 minutes duration).
No intervention (no video)
Outcomes
Primary Outcome Measures
Change in knowledge score
Secondary Outcome Measures
Change in "confidence to treatment" score, as indicated by participant response to questionnaire.
Measured on a scale from 1-10
Change in "satisfaction with the amount of information" score, as indicated by participant response to questionnaire.
Measured on a scale from 1-10
Change in "understandability of the information" score, as indicated by participants response to questionnaire.
Measured on a scale from 1-10
Full Information
NCT ID
NCT02445664
First Posted
May 8, 2015
Last Updated
May 12, 2015
Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02445664
Brief Title
Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment
Official Title
Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment - a Randomized, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
August 2014 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
November 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital
4. Oversight
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
Patient education, Video intervention
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
67 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Video intervention
Arm Type
Experimental
Arm Description
A tablet-administered educational video (10 minutes duration).
Arm Title
Control
Arm Type
No Intervention
Arm Description
No intervention (no video)
Intervention Type
Behavioral
Intervention Name(s)
Educational video
Intervention Description
Video: Information on osteoporosis and alendronate treatment.
Primary Outcome Measure Information:
Title
Change in knowledge score
Time Frame
Baseline and 2-week follow up
Secondary Outcome Measure Information:
Title
Change in "confidence to treatment" score, as indicated by participant response to questionnaire.
Description
Measured on a scale from 1-10
Time Frame
Baseline and 2-week follow up
Title
Change in "satisfaction with the amount of information" score, as indicated by participant response to questionnaire.
Description
Measured on a scale from 1-10
Time Frame
Baseline and 2-week follow up
Title
Change in "understandability of the information" score, as indicated by participants response to questionnaire.
Description
Measured on a scale from 1-10
Time Frame
Baseline and 2-week follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
12. IPD Sharing Statement
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Effect of a Tablet-administered Educational Video on Patients´ Knowledge on Osteoporosis and Treatment
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