NCT07292545Recruiting
Video-Based Proprioceptive Exercise Program in ALS
Examining the Effectiveness of Video-Based Proprioceptive Home Exercise Program in Amyotrophic Lateral Sclerosis Patients
Source: ClinicalTrials.gov · Last updated 18 Dec 2025
Brief summary (registry, in English)
In the project, it was aimed to evaluate the proprioceptive system in the disease, which is still mysterious and therefore has no curative treatment under current conditions, and to examine the effects of the video-based proprioceptive home exercise programme on trunk and limb control and daily life activity as well as trunk and limb control. The study was planned to include 20 patients with a definite diagnosis of ALS. Proprioceptive sensory examination will be performed again in these patients, who are currently being followed up with ALS diagnosis and whose physical examination including neurological examination has been performed in detail, and the "Revised Amyotrophic Lateral Sclerosis Functional Rating Scale" (R-ALSFRS) will be applied to the patients. Subsequently, the patients will be followed up by applying a video-based proprioceptive home exercise programme 3 days a week for 8 weeks. At the end of the 8th week, a detailed neurological examination including proprioceptive sensation will be performed and the R-ALSFRS scale will be applied. In addition, ALS quality of life scale will be applied to the patients before and after the home programme. The data obtained after the treatment programme will be analysed and interpreted.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 10 Jul 2025
- Start date
- 14 Jul 2025
- Primary completion date
- 1 Oct 2026
- Lead sponsor
- Tarsus University
- Diseases
- ALS (motor neurone disease)
- NCT number
- NCT07292545
What you commit to
- Study type: Interventional
- Planned participants: 20
- From 14 Jul 2025 to the primary completion date, 1 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- ALS patients with neurological, orthopedic or visual dysfunction mimicking ALS,
- Those who cannot complete active joint movements in the upper and lower extremities,
- ALS patients who do not agree to participate in the study will not be included in the study.
Who the study is looking for
- ALS patients aged 18-70
- Those with a definite ALS diagnosis according to the Gold Coast criteria
- Those who can sit independently
- Those who have no cognitive problems
- Those who agree to participate in the study will be included in the study.
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Tarsus University Coordinator of this site? Confirm its status | Mersin | Turkey (Türkiye) | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.