Validity and Reliability of Face-to-Face and Tele-Assessment of Core Stability and Functional Capacity
NCT ID: NCT07256873
Last Updated: 2025-12-03
Study Results
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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RECRUITING
36 participants
OBSERVATIONAL
2025-11-30
2026-03-30
Brief Summary
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In this study, 36 individuals with nonspecific chronic low back pain will complete core stability tests (plank, side plank, Biering-Sørensen test, and trunk flexor endurance test), functional capacity tests (Timed Up and Go, 30-Second Chair Stand, and 1-Minute Stair Climb), and questionnaires including the Visual Analog Scale and the Oswestry Disability Index. Assessments will be performed by the same physiotherapist first face-to-face in the clinic, then by tele-assessment, and tele-assessment will be repeated after 5-7 days to assess test-retest reliability.
The results are expected to show whether tele-assessment provides accurate and reliable measurements compared with traditional face-to-face evaluation. The findings may support the safe and evidence-based use of tele-assessment methods in physiotherapy practice for individuals with chronic low back pain.
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Detailed Description
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This study will include 36 individuals with nonspecific chronic low back pain. Participants will complete a series of core stability tests (plank test, side plank test, Biering-Sørensen test, and trunk flexor endurance test), functional capacity tests (Timed Up and Go, 30-Second Chair Stand, and 1-Minute Stair Climb), and clinical scales including the Visual Analog Scale and the Oswestry Disability Index. All assessments will be administered by the same physiotherapist. The first evaluation will be conducted face-to-face in the clinic. A second evaluation will be performed through tele-assessment using a secure video-communication platform, and a third tele-assessment will be conducted 5-7 days later to measure test-retest reliability.
The study aims to compare the results obtained from face-to-face and tele-assessment methods and to determine the validity and reliability of tele-assessment for core stability and functional capacity measurements in individuals with chronic low back pain. The findings are expected to contribute to the evidence-based use of tele-assessment in physiotherapy practice and support its integration into clinical decision-making for patients who have limited access to in-person evaluation.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Chronic Low Back Pain
Participants diagnosed with nonspecific chronic low back pain who will undergo core stability and functional capacity assessments using two methods: (1) face-to-face clinical evaluation and (2) tele-assessment via video communication platforms.
Assessment
This observational study compares two assessment methods used to evaluate core stability and functional capacity in individuals with chronic nonspecific low back pain. Participants undergo standardized clinical tests performed first through face-to-face assessment and then through tele-assessment using secure video communication platforms. The assessments include Plank Test, Side Plank Test, Biering-Sorensen Test, Trunk Flexor Endurance Test, Timed Up and Go (TUG), 30-Second Chair Stand Test, 1-Minute Stair Climb Test, Visual Analog Scale (VAS), and Oswestry Disability Index (ODI). No therapeutic intervention is administered; only evaluation procedures are performed.
Interventions
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Assessment
This observational study compares two assessment methods used to evaluate core stability and functional capacity in individuals with chronic nonspecific low back pain. Participants undergo standardized clinical tests performed first through face-to-face assessment and then through tele-assessment using secure video communication platforms. The assessments include Plank Test, Side Plank Test, Biering-Sorensen Test, Trunk Flexor Endurance Test, Timed Up and Go (TUG), 30-Second Chair Stand Test, 1-Minute Stair Climb Test, Visual Analog Scale (VAS), and Oswestry Disability Index (ODI). No therapeutic intervention is administered; only evaluation procedures are performed.
Eligibility Criteria
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Inclusion Criteria
* Must be between 18 and 65 years of age.
* Must be able to independently perform activities of daily living.
* Must not have had previous surgery for low back pain.
* Must be clinically fit to safely perform the tests specified in the research protocol.
* Must have access to the necessary technology (mobile phone, tablet, or computer, internet connection) to participate in in-person and tele-assessment sessions.
* Must be willing to participate in the study and provide written consent.
Exclusion Criteria
* History of neurological, rheumatological, cardiovascular, or pulmonary disease.
* Presence of severe scoliosis, kyphosis, or other structural spinal deformities.
* Acute pain, serious musculoskeletal injury, or orthopedic problem that prevents exercise.
* Inability to perform tests safely due to vision and/or hearing loss.
* Inability to follow instructions due to psychiatric or cognitive problems.
* Lack of technological infrastructure for online interviews and tele-assessments.
18 Years
65 Years
ALL
No
Sponsors
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Istinye University
OTHER
Responsible Party
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Sherouk Labeeb
Principal Investigator
Locations
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Kubra Kardeş
Istanbul, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ISTU-PT-CLBP-2025
Identifier Type: -
Identifier Source: org_study_id
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