Multiple Sclerosis Clinical Trial
Official title:
Intensive Multimodal Training for Persons With Multiple Sclerosis: Random Controlled Trial
The aim of this study was to evaluate the safety, feasibility and preliminary effects of a high-intensity rehabilitative multimodal training protocol carried out on treadmill on walking efficacy, mobility, balance, executive function, fatigue and health-related quality of life in a sample of persons with moderate to severe MS deficit of mobility compared to a control group that received a strengthening program of similar intensity.
Persons with multiple sclerosis can have various deficits, affecting many aspects of physical
and cognitive functioning often leading to low levels of physical activity in daily life.
These include poor endurance, muscle weakness, incoordination and poor balance and cognitive
deficits that can all lead to persistent mobility difficulties in daily life.
Given the importance of exercise and physical activity for persons with multiple sclerosis
that are already moderately to severely hampered by their locomotor ability and balance, the
setting up of intense functional mobility training that targets the main deficits, in
adjunction to a clinical rehabilitation usual care and under close supervision, may be a
viable way of increasing the level of physiological health and give a basis for the persons
to start their own activity pursuit outside of the rehabilitation clinic. Treadmill walking
has several benefits for mobility rehabilitation. First, it is a everyday task, walking.
Second it lends itself well to a dual task paradigm where other aspects of mobility, such as
equilibrium and cognitive factors can be addressed during walking. Third, even persons with
severe walking limitations can train walking at various speeds when on treadmill, holding
onto handrails and using safety harnesses that minimize the possibility of adverse events
during training. Further, the treadmill paradigm lends itself well to training with
progressive task difficulty, numerous rhythmic repetitions, and importantly it can include an
aerobic component to improve cardiorespiratory fitness. All of which should lead to improved
submaximal exercise tolerance and endurance, more functional mobility and consequently
increased ability to carry out activities of daily living.
Methods: A consecutive sample of 42 People with Multiple Sclerosis (PwMS) were recruited from
the outpatient/inpatient rehabilitation service of the Don Gnocchi Foundation. The study was
conducted in accordance with the Declaration of Helsinki and was approved by the ethics
committee of the Don Gnocchi Foundation. Subjects signed an informed consent form before the
beginning of the study.
The study design was a two arm randomized 2:1 controlled trial (see study flow chart in
Figure 1).
The participants were assessed before and after the rehabilitation period by researchers
blinded to group assignment.
Participants in both groups received 15- 20 treatments sessions lasting 30 minutes 5 times
per week by experienced physical therapists trained for the study. All participants also
followed their usual rehabilitation care protocols as planned.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05528666 -
Risk Perception in Multiple Sclerosis
|
||
Completed |
NCT03608527 -
Adaptive Plasticity Following Rehabilitation in Multiple Sclerosis
|
N/A | |
Recruiting |
NCT05532943 -
Evaluate the Safety and Efficacy of Allogeneic Umbilical Cord Mesenchymal Stem Cells in Patients With Multiple Sclerosis
|
Phase 1/Phase 2 | |
Completed |
NCT02486640 -
Evaluation of Potential Predictors of Adherence by Investigating a Representative Cohort of Multiple Sclerosis (MS) Patients in Germany Treated With Betaferon
|
||
Completed |
NCT01324232 -
Safety and Efficacy of AVP-923 in the Treatment of Central Neuropathic Pain in Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT04546698 -
5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis
|
||
Active, not recruiting |
NCT04380220 -
Coagulation/Complement Activation and Cerebral Hypoperfusion in Relapsing-remitting Multiple Sclerosis
|
||
Completed |
NCT02835677 -
Integrating Caregiver Support Into MS Care
|
N/A | |
Completed |
NCT03686826 -
Feasibility and Reliability of Multimodal Evoked Potentials
|
||
Recruiting |
NCT05964829 -
Impact of the Cionic Neural Sleeve on Mobility in Multiple Sclerosis
|
N/A | |
Withdrawn |
NCT06021561 -
Orofacial Pain in Multiple Sclerosis
|
||
Completed |
NCT03653585 -
Cortical Lesions in Patients With Multiple Sclerosis
|
||
Recruiting |
NCT04798651 -
Pathogenicity of B and CD4 T Cell Subsets in Multiple Sclerosis
|
N/A | |
Active, not recruiting |
NCT05054140 -
Study to Evaluate Efficacy, Safety, and Tolerability of IMU-838 in Patients With Progressive Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT05447143 -
Effect of Home Exercise Program on Various Parameters in Patients With Multiple Sclerosis
|
N/A | |
Recruiting |
NCT06195644 -
Effect of Galvanic Vestibular Stimulation on Cortical Excitability and Hand Dexterity in Multiple Sclerosis Patients
|
Phase 1 | |
Completed |
NCT04147052 -
iSLEEPms: An Internet-Delivered Intervention for Sleep Disturbance in Multiple Sclerosis
|
N/A | |
Completed |
NCT03594357 -
Cognitive Functions in Patients With Multiple Sclerosis
|
||
Completed |
NCT03591809 -
Combined Exercise Training in Patients With Multiple Sclerosis
|
N/A | |
Completed |
NCT03269175 -
BENEFIT 15 Long-term Follow-up Study of the BENEFIT and BENEFIT Follow-up Studies
|
Phase 4 |