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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04876105
Other study ID # 24.11.2020/24
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 25, 2020
Est. completion date October 15, 2021

Study information

Verified date January 2022
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Together with the guidance of health professionals try to obtain information from media, popular magazines and books and the internet regarding diseases and treatment methods in patients with low back pain with the development of technology. In parallel with this information which they obtained, they turn to different treatment methods. This study was carried on examining how pain duration affects treatment preferences in patients with low back pain.


Recruitment information / eligibility

Status Completed
Enrollment 155
Est. completion date October 15, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Individuals between the ages of 18-65 with complaints of low back pain and no communication problems were included in the study. Exclusion Criteria: - Individuals with any systemic, neurological and / or orthopedic disease diagnosed other than complaint of low back pain were excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Assesment of treatment preference
Multiple-choice survey questions were created by the researchers based on the studies in the literature regarding the pain and treatment preferences of the participants

Locations

Country Name City State
Turkey Pamukkale University Denizli

Sponsors (1)

Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of treatment preferences Multiple-choice survey questions were created by the researchers based on the studies in the literature regarding the pain and treatment preferences of the participants. In this survey, the patients were asked to state which of the treatment methods applied for low back pain they knew and which of these methods they preferred. 5 minutes
Secondary Visual Analog Scale Pain intensity 1 minute
Secondary Oswestry Disability Index Disability caused by low back pain 5 minutes
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