Prevalence Of Disability And Fear Avoidance Beliefs

March 12, 2026 updated by: Dina Abdelhady Hammad Attia Ahmed

Prevalence Of Disability And Fear Avoidance Beliefs Among Egyptian Physical Therapists With Chronic Non Specific Low Back Pain

Three hundred eighty -one egyptian physical therapists of both genders with age 25-55 years old in Cairo governorate who have worked for at least two years.The study will be conducted to investigate the prevalence of disability and fear avoidance beliefs among egyptian physical therapists with chronic non-specific low back pain (CNSLBP), and data will be collected through self-administered questionnaires distributed electronically.Participants were recruited from various public and private physical therapy centers and hospitals in Cairo .

Study Overview

Status

Enrolling by invitation

Detailed Description

  1. Sujects:

    Three hundred eighty -one egyptian physical therapists of both genders with age 25-55 years old in Cairo governorate who have worked for at least two years.The study will be conducted to investigate the prevalence of disability and fear avoidance beliefs among egyptian physical therapists with chronic non-specific low back pain (CNSLBP) , and BMI 18:30 kg/m2 and data will be collected through self-administered questionnaires distributed electronically.Participants were recruited from various public and private physical therapy centers and hospitals in Cairo .

  2. Instrumentation for assessment:

Patients will be assessed by:

  1. Fear-Avoidance Beliefs Questionnaire ( FABQ ) for assessing fear-avoidance beliefs in individuals with low back pain
  2. Oswestry Disability Index (ODI) for measurement of disability in patients with low back pain

Assessment procedures:

This study will include 381 subjects both male and female physical therapists who have worked for at least two years. The assessment will be performed one time for each participant by the same physiotherapist. All participants will first be checked to see if they are matching the inclusion and exclusion criteria after that they will inform consent.

A pretested, self-administered, structured questionnaire will be used for data collection. The survey examined demographic data, gender, age, weight, height, smoking habits, drinking habits, marital status, history of LBP in the last year, the duration of the last LBP, pain consultation at a hospital, history of LBP treatment in the last year, current occupation, history of heavy physical labor, duration of driving or riding, history of exercise, duration of sitting, and duration of standing .

  1. The Fear avidance beliefs Questionnaire (FABQ): will be sent to physical therapists working in Cairo. Participants will be selected from public and private physical therapy clinics in Cairo. Responses will be collected by an electronic survey tool (i.e.,Google Form) and exported for statistical analysis with SPSS.

    -Fear avoidance beliefs will be measured using the FABQ. It contains 16 items, scored from 0-6 (completely agree to completely disagree). It consists of two subscales, the physical activity subscale (FABQ PA), scored out of 24 (scores of ≤15 indicate low and >15 indicate high fear avoidance), and work (FABQ W), scored out of 42 points (scores of ≤34 indicate low and >34 indicate high fear avoidance) .

  2. Oswestry Disability Index (ODI): The ODI will be used to assess the functional disability in NSCLBP.

    • The questionnaire examines the level of disability in 10 everyday activities of daily living.
    • Pain intensity -Personal care -Lifting
    • Walking -Sitting -Standing
    • Sleeping -Sex (if applicable)
    • Social -Travel
    • Each component is assigned a value between 0 and 5, with 5 indicating the most disability. The index is calculated by dividing the total score by the range of scores and multiplying the result by 100 to get the index's percentage value .
    • Scores are calculated as follows: [total score/(5 x number of questions answered)] x 100% (Shirley Ryan AbilityLab, n.d.).
    • Interpretation:
    • Functional disability will be classified into the following five classes:
    • minimal disability (0-20)
    • moderate disability (21-40)
    • severe disability (1-60)
    • crippled (61-80); and
    • being bed-bound (81-100)

Study Type

Observational

Enrollment (Estimated)

381

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

      • Cairo, Egypt
        • Faculty of physical therapy

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

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

This study will target the egyptian physical therapists in Cairo governorate who have worked for at least two years. This cross-sectional study included a convenience sample of Egyptian physical therapists diagnosed with chronic non-specific low back pain (CNSLBP). Participants were recruited from various public and private physical therapy centers and hospitals in Cairo .

Description

Inclusion Criteria:

  • Male and female Egyptian physical therapists who have worked for at least two years.
  • Working age from 25 to 55 years .
  • Those experiencing localized pain from the lower margin of the twelfth rib to the lower gluteal folds for more than three months were included in the NS-CLBP .
  • Physical therapists who are fluent in English language.
  • BMI 18:30 kg/m2 .

Exclusion Criteria:

  • Participants with a history of orthopaedic spine disease or surgery were excluded .
  • cauda equina lesion, malignancy, infection, history of spinal surgeries, pregnancy, pain related to mensuration, and mental illness.

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
Prevalence of Disaility Among Egyptian Physical Therapists With Chronic Non Specific Low Back Pain
Time Frame: 1 month
  • Fear avoidance beliefs will be measured using the FABQ. It contains 16 items, scored from 0-6 (completely agree to completely disagree). It consists of two subscales, the physical activity subscale (FABQ PA), scored out of 24 (scores of ≤15 indicate low and >15 indicate high fear avoidance), and work (FABQ W), scored out of 42 points (scores of ≤34 indicate low and >34 indicate high fear avoidance)
  • Oswestrydisability examines the level of disability in 10 everyday activities of daily living. -Pain intensity -Personal care -Lifting -Walking -Sitting -Standing -Sleeping -Sex (if applicable) -Social -Travel (Physiopedia, n.d.). -Each component is assigned a value between 0 and 5, with 5 indicating the most disability. The index is calculated by dividing the total score by the range of scores and multiplying the result by 100 to get the index's percentage value .
1 month

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Dina Abdelhady Hammad, Bachaleor, Cairo University

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)

September 7, 2025

Primary Completion (Actual)

November 20, 2025

Study Completion (Estimated)

May 13, 2026

Study Registration Dates

First Submitted

September 22, 2025

First Submitted That Met QC Criteria

December 13, 2025

First Posted (Actual)

December 16, 2025

Study Record Updates

Last Update Posted (Actual)

March 13, 2026

Last Update Submitted That Met QC Criteria

March 12, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • PDAF

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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