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Core Stability Training in Multiple Sclerosis

Core Stability Training in Ambulant Individuals With Multiple Sclerosis: a Multi-centre Randomised Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01414725
Enrollment
100
Registered
2011-08-11
Start date
2011-08-31
Completion date
2013-07-31
Last updated
2014-03-24

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

Conditions

Multiple Sclerosis

Keywords

Multiple Sclerosis, Mobility, Balance, Core Stability, Physiotherapy

Brief summary

The primary purpose of this study is to determine whether a 12 week Pilates based core stability training programme is effective in improving balance, mobility and balance confidence in ambulant individuals with Multiple Sclerosis (MS).

Detailed description

The primary purpose of this study is to determine whether a 12 week Pilates based core stability training programme is effective in improving balance, mobility and balance confidence in ambulant individuals with Multiple Sclerosis (MS). The secondary aim is to determine the relative effectiveness of this 12 week Pilates based core stability training programme compared to a standardised physiotherapy exercise programme. Finally we intend to explore the underlying mechanisms of change associated with these exercise interventions by directly measuring changes in muscle thickness and activation in the deep abdominal core stabilising muscles of a sub-set of participants.

Interventions

Individualised face to face training sessions, delivered over 12 weeks, plus an individualised 15-minute daily home exercise programme will be provided. This will be undertaken by a neurological physiotherapist. The exercises will comprise a standardised programme of simple physiotherapy exercises which aim to improve trunk and pelvic stability, lower limb muscle length and strength, and balance and control of movement, as described by Barrett et al \[2009\]. Exercises will be progressed in response to the abilities of the individual. Each participant will receive a workbook with written and diagrammatic instructions describing their home exercise programme.

OTHERCore Stability Training

Individualised face to face training sessions, delivered over 12 weeks, plus an individualised 15-minute daily home exercise programme will be provided. This will be undertaken by a neurological physiotherapist with experience in the delivery of core stability training to people with MS. Exercises will be progressed in response to the abilities of the individual. Each participant will receive a workbook with written and diagrammatic instructions describing their home exercise programme.

OTHERRelaxation

Three face to face individualised relaxation sessions, provided at 4 weekly intervals, plus a 15-minute home programme based around an audio relaxation CD. Weekly telephone contact / support will be provided.

Sponsors

University of Plymouth
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Definite diagnosis of MS, according to McDonald's criteria * Aged 18 years or over * Able to walk independently with or without use of intermittent or constant unilateral assistance such as walking stick or orthotic brace

Exclusion criteria

* In relapse or relapse in previous three months * Any medical condition contra-indicating participation in core stability exercises * Score \< 6 on the Abbreviated Mental Test, as an indicator of those whose cognitive difficulties could interfere with the informed consent process, or the ability to fully engage in the exercise programme. * Current or recent (within past 6 months) participation in core stability exercises * Current involvement in another interventional research study

Design outcomes

Primary

MeasureTime frame
Change in 10 metre timed walk (10MTW)baseline (pre intervention), 12 weeks (immediately post intervention), 16 weeks ( one month follow-up)

Secondary

MeasureTime frame
Change in Functional Reach - forwards and lateralbaseline (pre intervention), 12 weeks (immediately post intervention), 16 weeks ( one month follow-up)
Change in Visual Analogue Scale (10 point) to determine Difficulty in carrying a drink when walking.baseline (pre intervention), 12 weeks (immediately post intervention), 16 weeks ( one month follow-up)
Change in Activities-specific Balance Confidence (ABC) Scalebaseline (pre intervention), 12 weeks (immediately post intervention), 16 weeks (one month follow-up)
Change in Multiple Sclerosis 12-item Walking Scalebaseline (pre intervention), 12 weeks (immediately post intervention), 16 weeks (one month follow-up)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026