- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05386212
The Impact of an Instructional Web-based Healthcare App for Relieving Back Pain From Spinal Compression Fractures
May 18, 2022 updated by: Pei-Hung Liao, National Taipei University of Nursing and Health Sciences
National Taipei University of Nursing and Health Science
With the expected rise of patients with osteoporosis-induced fractures, it has become increasingly urgent to design and use specialized health education materials aimed at easing pain and improving bodily functions
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
This study designed web-based dynamic pain relief instructions for women with spinal compression fractures.
We collected patients' pain rating data the day before, one month after, and three months after providing the instructions.
Study Type
Observational
Enrollment (Anticipated)
250
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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-
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Taipei, Taiwan
- Cheng Hsin General Hospital
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Taipei, Taiwan
- National Taipei University of Nursing and Health Science
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Peito
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Taipei, Peito, Taiwan, 112
- National Taipei University of Nursing and Health Science
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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
45 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
postmenopausal women
Description
Inclusion Criteria:
- postmenopausal women
Exclusion Criteria:
- postmenopausal women
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 |
Intervention / Treatment |
|---|---|
|
control
regular nursing care instructions
|
This study designed web-based dynamic pain relief instructions for women with spinal compression fractures.
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|
Expirement
web app healthcare instructions for relieving back pain
|
This study designed web-based dynamic pain relief instructions for women with spinal compression fractures.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of back pain, and qualitative of life between groups
Time Frame: 3 months
|
Follow-up observations of the control and experimental groups one month after the f intervention, as well as a significant difference between the data collected prior to the intervention and two months after the intervention
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Pei-Hung Liao, National Taipei University of Nursing and Health Sciences
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 (Actual)
May 12, 2022
Primary Completion (Anticipated)
December 1, 2022
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
May 10, 2022
First Submitted That Met QC Criteria
May 18, 2022
First Posted (Actual)
May 23, 2022
Study Record Updates
Last Update Posted (Actual)
May 23, 2022
Last Update Submitted That Met QC Criteria
May 18, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 108A-16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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