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NCT05386212 Clinical Trial

The Impact of an Instructional Web-based Healthcare App for Relieving Back Pain From Spinal Compression Fractures

Back Pain Lower Back Chronic Clinical Trial

Official title:
National Taipei University of Nursing and Health Science

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT05386212
Other study ID # 108A-16
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date May 12, 2022
Est. completion date December 1, 2022

Study information
Verified date May 2022
Source National Taipei University of Nursing and Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 250
Est. completion date December 1, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 45 Years to 80 Years
Eligibility Inclusion Criteria: - postmenopausal women Exclusion Criteria: - postmenopausal women

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• web app healthcare instructions for relieving back pain
This study designed web-based dynamic pain relief instructions for women with spinal compression fractures.

Locations
Country Name City State
Taiwan Cheng Hsin General Hospital Taipei
Taiwan National Taipei university of nursing and health science Taipei
Taiwan National Taipei university of nursing and health science Taipei Peito

Sponsors (2)
Lead Sponsor Collaborator
National Taipei University of Nursing and Health Sciences Cheng-Hsin General Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparison of back pain, and qualitative of life between groups 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
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