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Neurodynamic Interventions for Multiple Sclerosis

Not Applicable
Completed
Conditions
Multiple Sclerosis
Interventions
Other: Physical Therapy
Other: Physical Therapy plus Neurodynamic
Registration Number
NCT03595631
Lead Sponsor
Universidad Rey Juan Carlos
Brief Summary

A randomized, parallel-group, clinical trial will be conducted to compare the immediate effects of the inclusion of a neurodynamic intervention into a multimodal physiotherapy program on pressure pain sensitivity, pain and manual dexterity in patients with multiple sclerosis

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • a diagnosis of multiple sclerosis according to the modified McDonald criteria;
  • symptoms of paresthesia and lack of sensitivity in the upper extremity;
  • Expanded Disability Status Scale (EDSS) between 0 and 6.5 points;
  • absence of cognitive deficit.
Exclusion Criteria
  • any exacerbation of multiple sclerosis during the previous 3 months;
  • previous hand surgery or steroid injections treatment in the upper extremity;
  • multiple diagnoses on the upper extremity (e.g., cervical radiculopathy);
  • cervical, shoulder, or upper extremity trauma;
  • other comorbid musculoskeletal medical conditions;
  • mini-mental state examination <25

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Physical TherapyPhysical TherapyPatients will receive 5 session of multimodal physiotherapy treatment of 30min duration including low-load strength exercises, soft tissue mobilization and muscle-tendon stretching exercises twice per week.
Physical Therapy plus neurodynamicPhysical Therapy plus NeurodynamicPatients will receive 5 session of multimodal physiotherapy treatment of 30min duration including low-load strength exercises, soft tissue mobilization and muscle-tendon stretching exercises twice per week. In addition, they will also receive bilateral nerve slider neurodynamic interventions targeting the median, ulnar and radial nerves.
Primary Outcome Measures
NameTimeMethod
Changes in pressure pain sensitivityBaseline and one week after the last treatment session

Pressure pain threshold over the median, ulnar and radial nerves, second metacarpal and tibialis anterior

Secondary Outcome Measures
NameTimeMethod
Changes in upper extremity pain intensity before and after the interventionBaseline and one week after the last treatment session

A Numerical Pain Rate Scale (NPRS, 0-10) will be used to record the mean and the worst intensity of pain in te upper extremity

Changes in light touch detection thresholdBaseline and after treatmentBaseline and one week after the last treatment session

Light touch detection threshold will be assessed with a standardized set of modified twenty von Frey hairs

Changes in manual dexterityBaseline and one week after the last treatment session

Bilateral manual dexterity was bilaterally assessed using the nine-hole peg test

Trial Locations

Locations (1)

César Fernández-de-las-Peñas

🇪🇸

Alcorcon, Madrid, Spain

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