- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06875180
The Effects of Tele-Rehabilitation in Patients With Chronic Non-Specific Low Back Pain
August 2, 2025 updated by: Pınar Kuyulu
The Effect of Tele-Rehabilitation on Pain, Kinesiophobia and Disability in Patients With Chronic Non-Specific Low Back Pain
The aim of this study was to investigate the effect of telerehabilitation on pain, disability, kinesiophobia and normal range of motion in patients with chronic non-specific low back pain.
The study included 100 patients aged 18-64 years with chronic non-specific low back pain.
In our study, McKenzie extension exercises were applied to 50 patients online via the zoom platform and to 50 patients face-to-face in the clinical environment under the supervision of a physiotherapist in charge.
In our study, pain was assessed with the VAS, disability was assessed with the ODI, kinesiophobia was assessed with the TKS, and ROM was assessed with a goniometer.
As a result of our study, there was no statistically significant difference in VAS values between both groups, a statistically significant difference was observed in both groups according to the measurement times and the pain level decreased in both groups.
As a result of our study, there was no statistically significant difference in ODI values between both groups, a statistically significant difference was observed in both groups according to the measurement times and the level of disability decreased in both groups.
As a result of our study, there was no statistically significant difference between the two groups in TKS values and no difference was observed according to the measurement times in both groups.
As a result of our study, there was no statistically significant difference in ROM values between both groups, a statistically significant difference was observed in both groups according to the measurement times and ROM values increased.
In conclusion, telerehabilitation in patients with chronic non-specific low back pain is as effective as face-to-face exercise training in improving pain, disability and range of motion levels, but the effect of telerehabilitation on improving kinesiophobia has not been found.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of this study was to investigate the effect of telerehabilitation on pain, disability, kinesiophobia and normal range of motion in patients with chronic non-specific low back pain.
The study included 100 patients aged 18-64 years with chronic non-specific low back pain.
In our study, McKenzie extension exercises were applied to 50 patients online via the zoom platform and to 50 patients face-to-face in the clinical environment under the supervision of a physiotherapist in charge.
In our study, pain was assessed with the Visual Analogue Scale (VAS), disability was assessed with the Oswestry Disability Index (ODI), kinesiophobia was assessed with the Tampa Kinesiophobia Scale (TKS), and Range of Motion (ROM) was assessed with a goniometer.
As a result of our study, there was no statistically significant difference in VAS values between both groups (p>0.05), a statistically significant difference was observed in both groups according to the measurement times and the pain level decreased in both groups (p<0.05).
As a result of our study, there was no statistically significant difference in ODI values between both groups (p>0,05), a statistically significant difference was observed in both groups according to the measurement times and the level of disability decreased in both groups (p<0,05).
As a result of our study, there was no statistically significant difference between the two groups in TKS values (p>0,05) and no difference was observed according to the measurement times in both groups (p>0,05).
As a result of our study, there was no statistically significant difference in ROM values between both groups (p>0.05), a statistically significant difference was observed in both groups according to the measurement times and ROM values increased (p<0.05).
In conclusion, telerehabilitation in patients with chronic non-specific low back pain is as effective as face-to-face exercise training in improving pain, disability and range of motion levels, but the effect of telerehabilitation on improving kinesiophobia has not been found.
Study Type
Interventional
Enrollment (Actual)
100
Phase
- Not Applicable
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
-
-
-
Gaziantep, Turkey, 27090
- Sanko University
-
-
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
No
Description
Inclusion Criteria:
- Being between 18-64 years of age,
- Having non-specific low back pain for ≥3 months,
- Not having radicular symptoms related to low back pain
Exclusion Criteria:
- History of surgery on the spine and/or extremities,
- Diagnosis of malignancy,
- Orthopaedic and neurological disorders affecting the evaluation and treatment, - Psychiatric illness,
- Physical therapy for low back pain in the last six months,
- Being pregnant.
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Tele-rehabilitation group
Tele-rehabilitation exercise was applied to this group.
|
For this group, McKenzie extension exercises were applied to 50 patients online via the zoom platform.
|
|
Active Comparator: Face-to-face group
This group underwent conventional face-to-face exercise.
|
For this group, 50 patients face-to-face in the clinical environment under the supervision of a physiotherapist in charge.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Disability
Time Frame: 18 months
|
In our study, disability has assessed with the Oswestry Disability Index (ODI).
|
18 months
|
|
Pain intensity
Time Frame: 18 months
|
In our study, pain has assessed with the Visual Analogue Scale (VAS).
Scores range from 0 to 10
|
18 months
|
|
Kinesiophobia
Time Frame: 18 months
|
In our study, kinesiophobia has assessed with the Tampa Kinesiophobia Scale (TKS).
Scores range from 17 to 68 points.
|
18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Range of motion
Time Frame: 18 months
|
In our study, Range of Motion (ROM) has assessed with a goniometer.
|
18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Arzu Demirguc, PhD, Professor, Sanko 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)
December 10, 2023
Primary Completion (Actual)
June 30, 2025
Study Completion (Actual)
June 30, 2025
Study Registration Dates
First Submitted
January 29, 2025
First Submitted That Met QC Criteria
March 8, 2025
First Posted (Actual)
March 13, 2025
Study Record Updates
Last Update Posted (Actual)
August 5, 2025
Last Update Submitted That Met QC Criteria
August 2, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/25
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
The publication of the scientific article in a journal might be shared with other researchers.
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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