Effects of Upper Extremity-Focused Neuromuscular Training in People With Multiple Sclerosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-64
SponsorIstanbul Aydın University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Definite MS according to McDonald criteria,

18-64 years

RRMS,

EDSS < 4,

Disqualifiers

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,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Neuromuscular Exercise Training

    Other intervention

    This group will receive neuromuscular exercise training with 60-75 minute sessions per day, 2 days a week, for 8 weeks. Warm-up Program - 5 minutes Postural Control-Weight Transfer - 10-15 minutes Strength Training - 30-35 minutes Proprioception - Coordination - Reaction Speed 10-15 minutes Cool-down Program - 5 minutes

  • Conventional Exercise Training

    Other intervention

    This group will be given traditional strength exercise training consisting of 60-75 minute sessions per day, 2 days per week for 8 weeks. Warm-up Program - 5 minutes Strength Training - 30-35 minutes Manuel Dexterity - 15-20 minutes Cool-down Program - 5 minutes

Treatment groups

72 Participants
are divided into 3 treatment groups
Group A: NEGExperimental treatment 1 intervention
Group B: CEGActive comparator 1 intervention
Group C: CGNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Nine Hole Peg Test

To assess unilateral function of the upper extremity

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
2

Minnesota Manual Dexterity Test

To assess bilateral upper extremity function

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
3

Manual Ability Measure-36

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

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
4

Timed 25-Foot Walk

To assess lower extremity function

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

Secondary outcomes

1

Hand Held Dynamometer

To assess elbow muscle strength

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
2

Biodex Balance System

To assess postural sway

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
3

Laser-pointer Assisted Angle Reproduction Test

To assess of shoulder proprioception

Time frame
At the beginning, at the end of 8 weeks and 12 weeks
4

Finger Tapping Test

To assess upper extremity coordination

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

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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