Neurodynamic Interventions for Multiple Sclerosis
- Conditions
- Multiple Sclerosis
- Interventions
- Other: Physical TherapyOther: 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
- 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.
- 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
Group Intervention Description Physical Therapy Physical Therapy Patients 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 neurodynamic Physical Therapy plus Neurodynamic Patients 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
Name Time Method Changes in pressure pain sensitivity 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 Outcome Measures
Name Time Method Changes in upper extremity pain intensity before and after the intervention Baseline 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 threshold Baseline 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 dexterity Baseline 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