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Clinical Trials/NCT03595631
NCT03595631
Completed
Not Applicable

Effects of Neurodynamic Interventions to Multimodal Physical Therapy in Patients With Multiple Sclerosis

Universidad Rey Juan Carlos1 site in 1 country32 target enrollmentJuly 26, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Multiple Sclerosis
Sponsor
Universidad Rey Juan Carlos
Enrollment
32
Locations
1
Primary Endpoint
Changes in pressure pain sensitivity
Status
Completed
Last Updated
7 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
July 26, 2018
End Date
October 4, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

César Fernández-de-las-Peñas

Director of Department

Universidad Rey Juan Carlos

Eligibility Criteria

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

Outcomes

Primary Outcomes

Changes in pressure pain sensitivity

Time Frame: Baseline and one week after the last treatment session

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

Secondary Outcomes

  • Changes in upper extremity pain intensity before and after the intervention(Baseline and one week after the last treatment session)
  • Changes in light touch detection threshold(Baseline and after treatmentBaseline and one week after the last treatment session)
  • Changes in manual dexterity(Baseline and one week after the last treatment session)

Study Sites (1)

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