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The Effect of Virtual Reality on Fatigue and Functional Capacity in Patients With MS

CompletedNA

Sponsor: Istinye University

Conditions: Multiple Sclerosis, Multiple Sclerosis (MS) - Relapsing-remitting, Virtual Reality

Interventions: control group( physical therapy), Experemental group

Countries: Turkey (Türkiye)

This clinical trial aims to evaluate the effectiveness of virtual reality (VR) as a complementary intervention to traditional physical therapy for individuals diagnosed with Multiple Sclerosis (MS). MS is a chronic neurological condition that affects motor and cognitive functions, with fatigue being one of the most common and disabling symptoms. This study will assess whether the use of VR-based applications, in addition to standard physiotherapy, can reduce fatigue and improve functional capacity in individuals with MS. Participants will be randomly assigned to two groups: one group will receive conventional physiotherapy only, while the other will receive VR-based therapy alongside physiotherapy. The intervention period will last four weeks, and both groups will be evaluated using standardized outcome measures before and after the intervention. These include the Fatigue Severity Scale (FSS), the Timed Up and Go (TUG) test, and the 6-Minute Walk Test (6MWT). The study is designed to address a gap in current literature, as no prior research has specifically examined the impact of virtual reality on fatigue and functional performance in MS patients. The findings may provide valuable insights into innovative rehabilitation strategies that enhance patient outcomes and improve quality of life.

Eligibility overview

Sex: ALL

Age: 20 Years to 85 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

1. individuals diagnosed as MS by a physician
2. Expanded Disability Status Scale (EDSS): 2.0-6.5
3. Patient able to walk with or without the use of unilateral support (e.g., a cane)
4. Patient had not experienced a severe exacerbation of symptoms requiring medical intervention in the previous month
5. subjects had to have the cognitive capacity to assure the requisite cognitive ability
6. spasticity up to 2 on Ashworth scale.

Exclusion Criteria:

* 1\. cognitive disorders hampering the execution of the exercises/assessment, 2. Ability to maintain monopodalic-standing position for 10 s 3. cardiovascular disorders 4. orthopedic disorders that could negatively affect balance 5. uncorrected visual or auditory impairments 6. pregnancy

Locations (1)

Istanbul, Turkey (Türkiye)