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CompletedNCT06405802Updated May 10, 2024

Comparison of Technology-assisted and Face-to-face Assessment in Patients With Low Back Pain

An interventional study of Tele-evaluation in Low Back Pain, sponsored by Izmir Katip Celebi University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-10.

Sponsored by Izmir Katip Celebi University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled Aug 2022, registered May 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Although the concepts of telemedicine and tele-rehabilitation have been frequently emphasized in recent years, the evaluation part remains inadequate. There is no study investigating remote technology-based balance, mobility and strength assessments in patients with low back pain. Therefore, the aim of the study is; It is the examination of face-to-face and technology-based remote balance, mobility and strength assessment in patients with low back pain.

02

Conditions studied

  • Low Back Pain

Keywords

  • tele-evaluation
  • Low Back Pain
  • Face to face evaluation
03

In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's enrollment of 50 is below the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

Izmir Katip Celebi University is the lead sponsor of 191 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Those over the age of 18
  • People who can read and write
  • Patients who have not undergone surgery
  • Those whose body mass index is less than 30 m2/kg
  • Volunteering to participate in the study

Exclusion criteria

Exclusion criteria

  • Patients who underwent surgery due to disc herniation
  • Having any spinal pathology
  • Having an uncontrolled neurological and metabolic disease
  • Having a spinal deformity such as scoliosis or kyphosis
  • Those with serious orthopedic, vascular, neurological or psychiatric problems that affect balance
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Tele-evulation

    Face-to-face tests will be recorded by video and re-evaluation will be made over the video by another person who has not performed the tests. During technology-based remote evaluations, the evaluator will monitor the tests simultaneously via video. During technology-based remote evaluations, video recording will be made and a re-evaluation will be made over the video by another person who has not performed the tests.

    Other: Tele-evaluation

  • Experimental
    Face-to face evulation

    Face-to-face applications were carried out with individuals with low back pain who came to Bozyaka Training and Research Hospital and volunteered to participate in the study.

    Other: Tele-evaluation

Interventions

  • OtherTele-evaluation

    Evaluations will be carried out in two different environments: face-to-face in the clinic and remotely using technology. Face-to-face applications and remote evaluations using technology will be repeated once. Face-to-face applications will be made to individuals with low back pain who come to Bozyaka Training and Research Hospital and volunteer to participate in the study. Then, patients will be video-called at home, asked to perform the tests twice as taught, and recorded as a video.

    Also known as: Face to face evaluation

06

What researchers measure

Primary outcomes

  1. Oswestry disability index

    The Oswestry Disability Questionnaire is a self-assessment tool that allows patients to assess the various constraints encountered during their daily activities. Utilizing a comprehensive scoring system ranging from 0 to 100, higher scores on the questionnaire indicate a heightened level of disability.

    Time frame: An evaluation was made once at the beginning of the research.

  2. Timed-up and go test

    Simmonds et al. (1998) researched to ascertain the reliability of this test in swiftly and practically demonstrating functional status among patients with low back pain. The assessment involves the patient transitioning from seated to standing, traversing a 3-meter-long path, executing a turn, and returning to a seated posture. The duration of this performance is meticulously recorded

    Time frame: An evaluation was made once at the beginning of the research.

  3. Single Leg Stance Test

    This examination, focused on assessing balance and static standing capacity, also offers insights into individuals' susceptibility to falls. During the evaluation process, participants were instructed to elevate their foot on their unaffected side and sustain this position for as long as possible. The termination of the test was determined by either contact of the free leg with the ground or a notable increase in arm oscillations

    Time frame: An evaluation was made once at the beginning of the research.

  4. Thirty Second Chair Stand Test

    The Thirty Second Chair Stand Test is a validated and reliable assessment modality to gauge lower extremity strength (7). During the administration of this test, participants were tasked with repeatedly rising from and sitting back down on a chair within a 30-second timeframe, with the total number of repetitions recorded. A chair with a standardized sitting height of 43 cm was utilized for the assessments, and for safety precautions, it was positioned against a wall.

    Time frame: An evaluation was made once at the beginning of the research.

07

Study locations

1 site
  • Izmir Kâtip Çelebi University Vocational School of Health Services
    İzmir, Turkey
08

References and documents

Individual participant data

Plan to share: No — We aim to turn our research into an article and publish it in scientific journals.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 10, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06405802
Lead sponsor
Izmir Katip Celebi University
Collaborators
Bozyaka Training and Research Hospital, Dokuz Eylul University
Responsible party
Muhammed Zahid Uz (Lecturer, Izmir Katip Celebi University) — Principal investigator
First posted
May 8, 2024
Start date
Aug 10, 2022
Primary completion
Jan 15, 2024
Completion
Mar 10, 2024
Last update
May 10, 2024

Study contacts

Muhammed Zahid Uz, Master
study chair · Izmir Katip Çelebi University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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