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Effects of Endurance Training under Normobaric, Hypoxic Conditions on Fatigue in Patients with Multiple Sclerosis: Results of a Randomized, Prospective Pilot Study.

Effects of Endurance Training under Normobaric, Hypoxic Conditions on Fatigue in Patients with Multiple Sclerosis: Results of a Randomized, Prospective Pilot Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00006307
Enrollment
40
Registered
2014-07-17
Start date
2008-07-14
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

G35

Interventions

Group 1: therapy group: endurance training in normobaric hypoxia. symptom-specific inpatient rehabilitation (period of 14 days) + 12x 45 min endurance training on a bicycle ergometer, six days a week

Sponsors

Neurologisches Rehabilitationszentrum Quellenhof Bad Wildbad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 110 Years

Inclusion criteria

Inclusion criteria: patients over 18 years of age MS according to the McDonald criteria [19] chronic progressive or relapsing-remitting MS with walking ability (EDSS = 6) and self-reported fatigue Written informed consent

Exclusion criteria

Exclusion criteria: Patients with severe cardiopulmonary disease glucocorticosteroid therapy within the previous 30 days, serious functional limitations (i.e. high spasticity of the legs) limiting the ability to use the cycle ergometer as well as severe cognitive deficits that would have made it impossible to understand directions

Design outcomes

Primary

MeasureTime frame
fatigue: questionnaire: Würzburger Erschöpfungsinventar Multiple Sklerose (WEIMuS). Baseline, 7th and 14th day after baseline.

Secondary

MeasureTime frame
Endurance capacity: 6 minute walk test recorded at baseline and 14th day after baseline.

Countries

Germany

Contacts

Public ContactPeter Flachenecker

Neurologisches Rehabilitationszentrum Quellenhof Bad Wildbad

peter.flachenecker@sana.de07081 1730

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026