- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05862116
Impact of Health Literacy on Chronic Non-specific Low Back Pain
May 7, 2023 updated by: Mustafa Hüseyin Temel, Uskudar State Hospital
The Impact of Health Literacy on Quality of Life in Patients With Chronic Non-specific Low Back Pain: A Prospective Cohort Study
This prospective cohort study aims to assess the impact of health literacy on the quality of life in patients with chronic non-specific low back pain.
Study Overview
Detailed Description
This prospective cohort study will enroll patients with chronic non-specific low back pain.
Patients will be assessed using Turkey Health Literacy Scale-32, Short Form-36 Health Survey, and Oswestry Disability Index.
The correlation between health literacy and quality of life will be assessed with statistical tests.
Study Type
Observational
Enrollment (Anticipated)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mustafa H Temel, M.D.
- Phone Number: +905342714872
- Email: mhuseyintemel@gmail.com
Study Contact Backup
- Name: Fatih Bağcıer, M.D.
- Phone Number: 05442429042
- Email: bagcier_42@hotmail.com
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with chronic non-specific low back pain that gave consent to participate in the study.
Description
Inclusion Criteria:
-Chronic non-specific low back pain
Exclusion Criteria:
- Acute low back pain
- Radicular pain
- Spinal stenosis
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 |
|---|---|
|
Patients with chronic non-specific low back pain
Patients with chronic non-specific low back pain.
|
Patients will be asked to fill a survey form that consists of socio-demographic information, Turkish Health Literacy Scale -32, Short Form-36 Health Survey and Oswestry Disability Index.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The correlation between health literacy and quality of life
Time Frame: 1 day
|
Using the statistical analysis, this trial will assess the correlation between health literacy and quality of life.
The Turkey Health Literacy Scale-32 results and Short Form-36 Health Survey results will be tested for possible correlation.
Also, oswestry disability index and Turkey Health Literacy Scale-32 will also be tested for a possible correlation.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mustafa H Temel, M.D., Üsküdar State Hospital
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 (Anticipated)
July 1, 2023
Primary Completion (Anticipated)
October 1, 2023
Study Completion (Anticipated)
December 1, 2023
Study Registration Dates
First Submitted
May 7, 2023
First Submitted That Met QC Criteria
May 7, 2023
First Posted (Actual)
May 17, 2023
Study Record Updates
Last Update Posted (Actual)
May 17, 2023
Last Update Submitted That Met QC Criteria
May 7, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CNSLBP1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Individual participant data will be shared upon reasonable request by the corresponding author.
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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