Factors Affecting Quality of Life in Patient With Chronic Musculoskeletal Pain

March 31, 2023 updated by: Tugba Sahbaz, Kanuni Sultan Suleyman Training and Research Hospital

This study included patients who applied to the physical therapy and rehabilitation outpatient clinic and were diagnosed with chronic low back pain and osteoarthrosis and met the criteria for participation in the study.

Demografik datas, pain , Functional Limitations and Quality of Life wa evaluated.

Study Overview

Detailed Description

When treating diseases, clinicians traditionally aim for pain reduction and functional recovery. This is also true for chronic musculoskeletal diseases. However, the psychosocial support required to improve the general health perception of patients is becoming increasingly important. In clinical practice, it is essential to evaluate the quality of life and general well-being and to evaluate the patient completely biopsychosocially . Determining the factors affecting the quality of life is important in terms of contributing to the rehabilitation processes and treatment plans of CMP patients. In this direction, our study aims to examine the factors affecting the quality of life.

When treating diseases, clinicians traditionally aim for pain reduction and functional recovery. This is also true for chronic musculoskeletal diseases. However, the psychosocial support required to improve the general health perception of patients is becoming increasingly important. In clinical practice, it is essential to evaluate the quality of life and general well-being and to evaluate the patient completely biopsychosocially . Determining the factors affecting the quality of life is important in terms of contributing to the rehabilitation processes and treatment plans of CMP patients. In this direction, our study aims to examine the factors affecting the quality of life.

Study Type

Observational

Enrollment (Actual)

240

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • kanuni Sultan suleyman Research Hospital

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Male and female patients who applied to the physical therapy and rehabilitation outpatient clinic and were diagnosed with chronic low back pain and osteoarthrosis and meeting the criteria for participation in the study will be included in our study.

Description

Inclusion Criteria:

  • Aged between 18 and 65 years old
  • Clinical diagnosis of spondilosis and gonarthrosis-
  • Must not be surgical indication

Exclusion Criteria:

  • History of knee or back surgery
  • Detection of muscle weakness on physical examination
  • Presence of additional neurological disease that will affect the patient's mobilization and cognitive level
  • Presence of Cognitive impairment
  • Presence of Chronic pain of nonmusculoskeletal origin (gynocological, retroperitoneal, abdominal)
  • Being treated for depression

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Severity
Time Frame: Baseline
The severity of rest pain and activity pain experienced by the patients in the last 1 week will be evaluated by VAS, which is a numeric rating scale. The highest pain intensity is 10, o no pain, 5 will be scored as moderate pain. Higher scores mean more pain intensity
Baseline
Functioal Limitation
Time Frame: baseline

Roland Morris questionare (RMQ) will be used for disability assessment in patients with chronic low back pain.Roland Morris questionare evaluates functional limitation due to low back pain. The total maximum score is 24. It includes a total of 24 items questioning patients' mobility, self-care and sleep status.

Disability in patients with knee osteoarthritis will be evaluated with the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC).WOMAC; It is a 24-item scale that examines three dimensions: pain, stiffness and physical function. Higher scores mean more disability

baseline
Health-related quality of life
Time Frame: Baseline
The Short Form Health Questionnaire (SF-36) questionnaire, which examines health-related quality of life under eight sub-titles; It consists of 36 items. The SF36 questionnaire will be used in the study.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Actual)

March 27, 2022

Primary Completion (Actual)

March 31, 2023

Study Completion (Actual)

March 31, 2023

Study Registration Dates

First Submitted

February 3, 2022

First Submitted That Met QC Criteria

March 17, 2022

First Posted (Actual)

March 28, 2022

Study Record Updates

Last Update Posted (Actual)

April 4, 2023

Last Update Submitted That Met QC Criteria

March 31, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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