Investigation of the Relationship of Pain Perception and Pain Belief With Age in People With Chronic Lack Pain

Sponsor
Uskudar University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05997368
Collaborator
(none)
210
1

Study Details

Study Description

Brief Summary

This study was planned to investigate the relationship between pain perceptions and pain beliefs of individuals in different age groups with chronic low back pain and symptom severity.

Condition or Disease Intervention/Treatment Phase
  • Other: Survey1
  • Other: Survey2
  • Other: Survey3

Detailed Description

The study will be conducted as an observational descriptive and cross-sectional research. Participants will be recruited after the purpose and content of the research are explained by the researchers, their written consent is read, and the volunteers who agree to be included in the study are given their written consent. The data collection process was carried out face-to-face and via a Google Forms survey over the internet, and will be conducted with the participants face-to-face and online. In the study; The pain beliefs questionnaire (PBQ), the centrality of pain scale (COPS) and the numerical rating scale (NRS-11) will be used.

Study Design

Study Type:
Observational
Anticipated Enrollment :
210 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Investigation of the Relationship of Pain Perception and Pain Belief With Age in People With Chronic Lack Pain
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
young group

Participants aged 18-39

Other: Survey1
As a research, it was planned to be a quantitative research. Data collection will be conducted through online and face-to-face surveys. Scales and forms to be found and used in the research: The Pain Beliefs Questionnaire-PBQ, Numerical Rating Scale (NRS-11) and The Central Of Pain Scale-COPS. By handing out the paper format to the participants and uploading it to the Google Forms system online, it can be downloaded from mail, social media or mobile phone applications such as message, Mail, etc. They will be asked to participate in the study by accessing

middle-aged group

Participants aged 40-56

Other: Survey2
As a research, it was planned to be a quantitative research. Data collection will be conducted through online and face-to-face surveys. Scales and forms to be found and used in the research: The Pain Beliefs Questionnaire-PBQ, Numerical Rating Scale (NRS-11) and The Central Of Pain Scale-COPS. By handing out the paper format to the participants and uploading it to the Google Forms system online, it can be downloaded from mail, social media or mobile phone applications such as message, Mail, etc. They will be asked to participate in the study by accessing

elderly group

Participants aged 57-79

Other: Survey3
As a research, it was planned to be a quantitative research. Data collection will be conducted through online and face-to-face surveys. Scales and forms to be found and used in the research: The Pain Beliefs Questionnaire-PBQ, Numerical Rating Scale (NRS-11) and The Central Of Pain Scale-COPS. By handing out the paper format to the participants and uploading it to the Google Forms system online, it can be downloaded from mail, social media or mobile phone applications such as message, Mail, etc. They will be asked to participate in the study by accessing

Outcome Measures

Primary Outcome Measures

  1. The numeric rating scale - NRS-11 [2 weeks]

    When using the NRS-11, patients are asked to rate their pain on a scale of 0 to 10; where using integers (11 integers including zero) 0 represents "no pain" and 10 represents "worst possible pain". Based on prior studies and clinical experience of use, pain screening scores NRS-11 scores as mild (1-3) are classified as moderate (4-6) or severe (7-10).

  2. The centrality of pain scale - COPS) [2 weeks]

    It is a short 10-item self-report scale designed to assess the centrality of pain. COPS scores are significantly correlated with the clinician's assessment of individual-reported pain severity, disability, mental health, quality of life, and how well the patient's pain is controlled. Each item is rated on a five-point Likert scale. It is a 10-item questionnaire (1: strongly disagree, 2: disagree, 3: neither agree nor disagree, 4: agree, 5: strongly agree). Items 2, 4 and 9 are evaluated in reverse. The resulting value is the sum of all item scores. Higher scores indicate more "central" pain. The highest possible score is 50 and the lowest possible score is 10.

  3. The pain beliefs questionnaire - PBQ [2 weeks]

    Two subtests of the test were created: the 8-item Organic Beliefs subtest and the 4-item Psychological Beliefs subtest. The item numbers of both subtests are listed as follows: Organic Beliefs: items 1, 2, 3, 5, 7, 8, 10, 11, Psychological Beliefs: Items 4, 6, 9, 12. The test takers are asked to indicate the most appropriate one for the participants from 6 options ranging from 1st "never" to 6th "always". The marked scores range from 1 to 6 for each item. The score collected for each subtest is calculated by taking the items in that subtest and summing them up and dividing the numbers by the number of items related to that subtest. An increase in the value calculated from the sub-dimension of the scale indicates that the belief in pain belonging to the sub-dimension is high, and a decrease in the value indicates low pain belief in the sub-dimension.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • having low back pain for at least the past three months

  • be between the ages of 18-79.

Exclusion Criteria:
  • Those outside the age limit of 18-79 and illiteracy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Üsküdar Unıversıty Istanbul Turkey

Sponsors and Collaborators

  • Uskudar University

Investigators

  • Study Chair: Mahsun EKİNCİ, Uskudar University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Öğr. Üyesi Ömer Şevgin, assistant professor, Uskudar University
ClinicalTrials.gov Identifier:
NCT05997368
Other Study ID Numbers:
  • Uskudar67
First Posted:
Aug 18, 2023
Last Update Posted:
Aug 23, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Öğr. Üyesi Ömer Şevgin, assistant professor, Uskudar University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2023