The Effect of Clinical Monitoring Software on Symptoms in Patients With Chronic Low Back Pain
CompletedNot applicableNCT05816824
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The aim of this randomised controlled trial is to compare the effectiveness of two different telerehabilitation assessment methods in patients with chronic low back pain. The control group will receive a video exercise-based rehabilitation protocol with telerehabilitation. The intervention group will be followed up with the same protocol plus symptom monitoring software called PhysioAnalyst which provides visual feedback. The evaluation of outcome measures will be performed on the control group through the PhysioAnalist programme without visual feedback and on the intervention group through the PhysioAnalist programme with visual feedback.
Study details
- Official title
- The Effect of Visual Feedback Based Clinical Monitoring Software on Clinical and Psychosocial Symptoms in Patients With Chronic Low Back Pain
- Conditions
- Interventions
- Other: Symptom monitoring software via visual feedback
- Sponsor
- Muğla Sıtkı Koçman University
- Start date
- 2023-04-30
- Primary completion
- 2023-07-05
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Individuals with low back pain for more than 3 months and diagnosed with chronic low back pain * Adult patients aged between 18 and 65 years * Individuals without a radicular symptom * Patients who can understand and respond to verbal commands and who do not have hearing or speech problems or psychiatric problems that may prevent communication * Patients who have devices with sufficient requirements to receive the exercise programme and assessments offered by telerehabilitation Exclusion Criteria: * Spinal surgery history * Presence of malignancy * Presence of other orthopaedic and/or neurological diseases that may affect the assessment and treatment * Pregnant women or women with suspected pregnancy * Patients who did not sign the consent form required for participation in the study
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05816824