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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06125496
Other study ID # 60116787-020/92289
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 25, 2019
Est. completion date December 28, 2021

Study information

Verified date November 2023
Source Alanya Alaaddin Keykubat University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study was to examine the relationship between pain management, kinesiophobia, physical activity and disability level in patients with chronic low back pain (CLBP) in different genders. Eighty-two patients with CLBP (42 females, 42 males) between the ages of 20-60 participated in the study. Pain management strategies were determined by Pain Coping Questionnaire (PCQ). Tampa Scale for Kinesiophobia for perception of kinesiophobia, Oswestry Disability Index for disability due to pain and International Physical Activity Questionnaire-Short Form (IPAQ-SF) for the physical activity level were used.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date December 28, 2021
Est. primary completion date November 20, 2021
Accepts healthy volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - Individuals who are between 20 and 60 years old, - Experienced low back pain lasting longer than 3 months, and had no problems with reading, writing, and comprehension were included in the study. Exclusion Criteria: - Individuals who underwent surgery for low back pain, - Had any diagnosed spinal problem, - Who were pregnant, - And who had communication problems were not included in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pain management
Investigation of relationship between kinesiophobia, physical activity and disability level and pain management in patients with CLBP

Locations

Country Name City State
Turkey Pamukkale University Denizli

Sponsors (1)

Lead Sponsor Collaborator
Alanya Alaaddin Keykubat University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Coping Questionnaire (PCQ) The scale assesses how chronic pain patients cope with organic or psychogenic pain. The scale consists of four subdimensions that are self-coping, helplessness, conscious cognitive interventions, and seeking medical help, and 29 items. The self-report scale consists of a 4-point Likert scale (0: never, 3: often). From 25 December 2019 to 10 November 2021
Secondary Visual Analogue Scale (VAS) Subjects were asked to mark the severity of pain on a 10-cm line. The lowest point indicated the least severity of pain, and the highest point indicated the maximum pain value. From 25 December 2019 to 10 November 2021
Secondary Oswestry Disability Index (ODI) It consists of 10 items measuring the severity of pain, personal care, lifting, walking, sitting, standing, social life, sleeping, traveling, and degree of pain. Each item is scored between 0-5. The higher the total score, the higher the degree of disability. The maximum score is 50 points. From 25 December 2019 to 10 November 2021
Secondary Tampa Scale of Kinesiophobia (TSK) The scale is scored between 17 and 68 using a 4-point Likert type scale scoring system. A high score on the scale indicates a high level of kinesiophobia. From 25 December 2019 to 10 November 2021
Secondary International Physical Activity Questionnaire-Short Form (IPAQ -SF) The questionnaire provides information on time spent walking, moderate to vigorous activity, and vigorous activity. Time spent sitting is included as a separate question. The total score calculation includes the sum of time (minutes) and frequency (days) of walking, moderate activity, and vigorous activity. From 25 December 2019 to 10 November 2021
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