Skip to main content
Clinical Trials/NCT06712342
NCT06712342
Not yet recruiting
Not Applicable

Effects of Upper Extremity-Focused Neuromuscular Exercise Training on Physical and Cognitive Functions in People With Multiple Sclerosis (NExTUp)

Istanbul Aydın University0 sites72 target enrollmentNovember 30, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Multiple Sclerosis
Sponsor
Istanbul Aydın University
Enrollment
72
Primary Endpoint
Nine Hole Peg Test
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The effectiveness of upper extremity focused neuromuscular exercise training in early stage people with MS will be investigated. People with MS enrolled in the study will be randomly assigned to three groups: Neuromuscular Exercise Group (NEG), Conventional Exercise Group (CEG), and Control Group (CG). All three groups will be assessed with primary and secondary outcome measures at baseline, week 8, and week 12. NEG, CEG, and CG will be initially assessed for upper extremity function, cognitive function, lower extremity function, grip strength, proximal muscle strength, sensation, coordination, fatigue, postural sway, and core muscle strength and endurance. Then, NEG will receive clinically supervised upper extremity focused neuromuscular exercise training with a minimum of 60 minutes of session time, 2 days a week for 8 weeks. This exercise training includes steps for postural control, weight transfer, proximal and distal muscle strengthening, proprioception, coordination and reaction speed. Similarly, CEG will receive clinically supervised traditional upper extremity exercise training, twice a week for 8 weeks, with a minimum of 60 minutes of session time. This exercise training includes strengthening with the band and manuel dexterity exercises. In both groups, stretching and mobility exercises will be added to the warm-up and cool-down exercises before and after the program. During this process, CG will be on the waiting list. At the end of 8 weeks, all three groups will be re-evaluated. After the exercise training, follow-up will be done and evaluations will be repeated in the 12th week. This study will provide evidence on the effects of upper extremity-focused neuromuscular exercise training on physical and cognitive functions in early-stage people with MS compared to traditional treatment approaches.

Registry
clinicaltrials.gov
Start Date
November 30, 2024
End Date
December 29, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Aydın University
Responsible Party
Principal Investigator
Principal Investigator

Uğur OVACIK

PT, MSc

Istanbul Aydın University

Eligibility Criteria

Inclusion Criteria

  • Definite MS according to McDonald criteria,
  • 18-64 years
  • EDSS \< 4,
  • Minimal or moderate upper extremity involvement

Exclusion Criteria

  • Having an attack in the last three months,
  • Mini Mental Test \<24 or visual deficit,
  • Other medical conditions accompanying MS (cardiac, orthopedic or rheumatic, etc.),
  • Being pregnant or breastfeeding,
  • Doing regular exercise - receiving physiotherapy,
  • Having spasticity of 2 or more in the upper extremity

Outcomes

Primary Outcomes

Nine Hole Peg Test

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess unilateral function of the upper extremity

Minnesota Manual Dexterity Test

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess bilateral upper extremity function

Manual Ability Measure-36

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess upper extremity function. A higher score indicates better hand function.

Timed 25-Foot Walk

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess lower extremity function

Symbol Digit Modalities Test

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess cognitive function

Hand Dynamometer

Time Frame: At the beginning, at the end of 8 weeks and 12 weeks

To assess hand grip strength

Secondary Outcomes

  • Hand Held Dynamometer(At the beginning, at the end of 8 weeks and 12 weeks)
  • Biodex Balance System(At the beginning, at the end of 8 weeks and 12 weeks)
  • Laser-pointer Assisted Angle Reproduction Test(At the beginning, at the end of 8 weeks and 12 weeks)
  • Finger Tapping Test(At the beginning, at the end of 8 weeks and 12 weeks)
  • Fatigue Severity Scale(At the beginning, at the end of 8 weeks and 12 weeks)
  • Plank(At the beginning, at the end of 8 weeks and 12 weeks)
  • Curl-up(At the beginning, at the end of 8 weeks and 12 weeks)

Similar Trials