ClinicalTrials.Veeva

Menu

Multiple Sclerosis Rehabilitation Study

M

Melbourne Health

Status

Completed

Conditions

Multiple Sclerosis

Treatments

Behavioral: Speech pathology
Behavioral: Physiotherapy
Behavioral: Occupational therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT00202254
MelbUni HREC 040334
HREC 2004.101

Details and patient eligibility

About

The effects of routine rehabilitation in MS patients versus no rehabilitation.

Full description

Routine rehabilitation inervention in patients with MS. This comprises of medical and nursing input, physiotherapy, occupational therapy, speech pathology, neuropsychology, compared with a "control" group on the waiting list for rehabilitation intervention. Duration of intervention is 6 weeks.

Sex

All

Ages

19 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of MS (Paty)- Community dwelling participants with known neurological and psychological deficits per EDSS groups.- Age 19-64 years.- Male and female participants.- Residing within 60kms of metropolitan Melbourne.- Have mobility problem.- Adequate cognition (KFS=2).

Exclusion criteria

  • Patients residing in nursing home and other residential care.- Those with severe cognitive problems KFS>2.-

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems