Factors Associated With Quality of Life in Chronic Low Back Pain

NCT ID: NCT06694493

Last Updated: 2025-08-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

174 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-11-29

Study Completion Date

2025-03-22

Brief Summary

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The aim of this study was to identify and validate the factors that may affect quality of life in patients with chronic low back pain.

Detailed Description

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Participants between the ages of 18-65, who are willing to participate in the study and have low back pain for more than 3 months will be included in the study. The necessary demographic information will be obtained with a data form. For the evaluation; Visual Analogue Scale (VAS), Tampa Kinesiophobia Scale, Fear-Avoidance Beliefs Questionnaire, Roland-Morris Disability Questionnaire, Beck Depression Scale, Self-Efficacy for Managing Chronic Disease 6-Item Scale, Coping Strategies Inventory Short Form (CSI-SF), Pain Catastrophising Scale, Pittsburgh Sleep Quality Index, Short Form - 36 (Quality of Life Questionnaire) will be used. The data obtained in the study will be entered into SPSS 17 package programme (Greasley, 2007). Minimum-maximum values, arithmetic mean and standard deviation will be used to evaluate numerical data, and frequency distributions and percentages will be used to summarise categorical data. The data of the study will be analysed using Analysis of Moment Structures (AMOS) statistical package programmes. In all analyses, p\<0.05 will be considered statistically significant.

Conditions

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Chronic Low-back Pain (cLBP)

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Volunteering to participate in the study
* Having low back pain for more than 3 months
* Being between the ages of 18-65

Exclusion Criteria

* History of surgery in the spinal region
* Rheumatoid arthritis
* Tumour
* Autoimmune disease
* Neurological disease
* Psychiatric or cognitive impairment
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kutahya Health Sciences University

OTHER

Sponsor Role lead

Responsible Party

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Emrah Afsar

Phd

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Emrah Afsar, Phd

Role: PRINCIPAL_INVESTIGATOR

Kutahya Health Science University

Locations

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Kutahya Health Science University

Kütahya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2024-d

Identifier Type: -

Identifier Source: org_study_id

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