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Innovative training method in patients with Multiple Sclerosis and Spinal Cord Injury, a pilot study.

Innovative training method in patients with Multiple Sclerosis and Spinal Cord Injury, a pilot study. - Innovative training method in MS and SCI, a pilot study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46786
Enrollment
30
Registered
2018-03-30
Start date
2018-04-04
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

incomplete dwarslaesies Multiple Sclerosis (MS) Spinal Cord Injury (SCI)

Interventions

None listed

Sponsors

Libra Revalidatie & Audiologie
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Multiple Sclerosis (MS) -EDSS * 6.5 (needs mainly support on two sides or support tools to walk 20 meters (EDSS

Exclusion criteria

Exclusion criteria: - Contra-indications to perform a progressive cardiopulmonary exercise test (CPET) (Lausanne protocol ); - Abnormalities detected during the CPET which contra-indicate high intensity physical activities; - Pregnancy; - Unable to complete the full intervention based on time investment; - Essential changes in medication during the intervention period (e.g. disease-modifying drugs in MS); - Use of beta-blockers; - MS Relapse during the intervention period; - Malignant tumor as cause of SCI; - Any premorbid (before diagnosis of MS/SCI) progressive neuromuscular or brain disease.

Design outcomes

Primary

MeasureTime frame
Main study parameters: Primary parameters are: - aerobic capacity (progressive cardiopulmonary exercise test) - physical performance (Stair Climb Test, Progressive Isoinertial Lifting Evaluation, Sit To Stand test, Timed-up-and-Go test, 6 minute walk test maximal distance).

Secondary

MeasureTime frame
Secondary parameters are: - maximal muscle strength (1RM handgrip, 1RM legpress), - walking efficiency (6 minute walk test at comfortable speed), - fatigue (Fatigue Severity Scale (FSS), - quality of life (Short Form (36) Health Survey (SF-36), and Multiple Sclerosis Impact Scale (MSIS-29)), - feasibility of the program (questionnaire developed for this study). *

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)