- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01772459
Paper vs. Internet (P vs I)
June 20, 2014 updated by: University of British Columbia
Internet-administered Adolescent Scoliosis Questionnaires Compared With Traditional Pencil and Paper Versions: a Randomized Crossover Design
Research has shown that questionnaires completed on the internet have the potential to provide more complete and honest data with fewer errors in a more efficient manner than questionnaires completed using the paper and pencil format.
Despite the numerous advantages of internet-administered questionnaires, it is important to make sure that the internet questionnaires will yield comparable results to the well-established paper and pencil versions.
No one has studied internet administration of scoliosis specific questionnaires in adolescents with scoliosis.
The investigators will test whether the internet administration of scoliosis questionnaires is as reliable as the traditional paper and pencil version.
The investigators predict that the internet-administered questionnaire will provide the same reliability as the paper-administered questionnaires.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
139
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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British Columbia
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Vancouver, British Columbia, Canada, V6H 3V4
- British Columbia Children's Hospital
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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
10 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adolescents with idiopathic scoliosis will be asked to participate during visits to the orthopaedic spine clinic at BC Children's Hospital
Description
Inclusion Criteria:
- Aged 10-18
- Male or female
- Diagnosis of Adolescent or Juvenile Idiopathic Scoliosis
- Home access to computer and internet
- Capable or oral and written communication in English
Exclusion Criteria:
- Unable to communicate in English
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
Cohorts and Interventions
Group / Cohort |
|---|
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Paper/Paper
This group will complete paper questionnaires at baseline and two week follow up.
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Paper/Internet
This group will complete paper questionnaires at baseline and internet questionnaires at two week follow up.
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Internet/Paper
This group will complete internet questionnaires at baseline and paper questionnaires at two week follow up.
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Internet/Internet
This group will complete internet questionnaires at baseline and two week follow up.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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To test the reliability of the internet-administered PODCI and SRS-30 questionnaires in adolescents with idiopathic scoliosis
Time Frame: 2 weeks
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The reliability of internet-administered questionnaires will be determined by comparison to standard paper questionnaire implementation.
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2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Chris Reilly, MD, FRCSC, University of British Columbia
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, 2010
Primary Completion (Actual)
November 1, 2013
Study Completion (Actual)
November 1, 2013
Study Registration Dates
First Submitted
January 17, 2013
First Submitted That Met QC Criteria
January 18, 2013
First Posted (Estimate)
January 21, 2013
Study Record Updates
Last Update Posted (Estimate)
June 23, 2014
Last Update Submitted That Met QC Criteria
June 20, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H10-01785
- CW10-0184 (Other Identifier: UBC C&W Research Ethics Board)
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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