Skip to content

Clinical Pilates for Balance and Function in Multiple Sclerosis

Effectiveness of a Clinical Pilates Programme on Static and Dynamic Balance in Individuals With Multiple Sclerosis: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07800039
Acronym
MS-PILATES
Enrollment
21
Registered
2026-09-02
Start date
2024-05-30
Completion date
2024-09-10
Last updated
2026-09-09

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

Conditions

Multiple Sclerosis

Keywords

Clinical Pilates, Physiotherapy, Balance, Postural Control, Rehabilitation, Functional Mobility

Brief summary

This randomized controlled trial evaluated the effects of an 8-week Clinical Pilates program on balance and physical function in individuals with multiple sclerosis (MS). Participants were randomly allocated to one of three groups: Clinical Pilates, conventional exercise-based physiotherapy, or a control group receiving postural guidance without a structured rehabilitation program. The two intervention groups completed 16 supervised exercise sessions over 8 weeks. Outcomes included static and dynamic balance, functional mobility, lower-limb motor function, fatigue, and exercise-related motivation. Assessments were conducted at baseline, after 4 and 8 weeks, and at a one-month follow-up.

Interventions

BEHAVIORALClinical Pilates-Based Rehabilitation

Participants received an 8-week Clinical Pilates-based rehabilitation program comprising 16 sessions, delivered twice weekly with a minimum interval of 48 hours between sessions. Each session lasted approximately 60 minutes and included mobility and breathing exercises, strengthening, balance and coordination exercises, trunk control, core activation, body awareness, and stretching. Exercises were performed in standing, sitting, supine, prone, and side-lying positions. Exercise intensity and complexity were progressively adjusted according to individual ability.

BEHAVIORALConventional Exercise-Based Physiotherapy

Participants received an 8-week conventional exercise-based physiotherapy program comprising 16 sessions, delivered twice weekly with a minimum interval of 48 hours between sessions. Each session lasted approximately 60 minutes and included progressive strengthening, postural control, sensory integration, balance, and functional training. Exercises progressed from stable to more demanding balance and functional activities, with difficulty individually adjusted according to each participant's abilities and performance.

Sponsors

University of Patras
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

The principal investigator remained blinded to participants' group allocation during data analysis. Participant data were coded and analyzed without access to identifying information or knowledge of group assignment.

Intervention model description

Participants were randomly assigned in a 1:1:1 ratio to one of three parallel groups: Clinical Pilates, conventional exercise-based physiotherapy, or control.

Eligibility

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

Inclusion criteria

* Adults with a diagnosis of multiple sclerosis * Ability to maintain an upright standing position * Mini-Mental State Examination (MMSE) score \>24

Exclusion criteria

* Presence of neurological disorders other than multiple sclerosis * Lower-limb and/or spinal surgery within the previous year * History of heart failure * Uncontrolled hypertension

Design outcomes

Primary

MeasureTime frameDescription
Change in Center of Pressure Sway AreaBaseline, Week 4, Week 8, and 1-month follow-upCenter of pressure (CoP) sway area was assessed using a Bertec force platform during six standing conditions: feet together with eyes open, feet together with eyes closed, single-leg stance on the right and left leg, and tandem stance with the right and left foot leading. CoP sway area was used as a measure of static postural control, with lower values indicating less postural sway.
Change in Mini-BESTest ScoreBaseline, Week 4, Week 8, and 1-month follow-upDynamic balance was assessed using the Mini-Balance Evaluation Systems Test (Mini-BESTest), a 14-item clinical measure assessing anticipatory postural adjustments, reactive postural control, sensory orientation, and dynamic gait. The total score ranges from 0 to 28 points, with higher scores indicating better balance performance.

Secondary

MeasureTime frameDescription
Change in Center of Pressure DisplacementBaseline, Week 4, Week 8, and 1-month follow-upCenter of pressure (CoP) displacement in the mediolateral (ML) and anteroposterior (AP) directions was assessed using a Bertec force platform during six standing conditions: feet together with eyes open, feet together with eyes closed, single-leg stance on the right and left leg, and tandem stance with the right and left foot leading. Lower displacement values indicate less postural sway.
Change in Functional Gait Assessment (FGA) ScoreBaseline, Week 4, Week 8, and 1-month follow-upDynamic balance during walking was assessed using the Functional Gait Assessment (FGA). The FGA consists of 10 items assessing the ability to modify gait while performing different walking tasks. Each item is scored from 0 to 3, giving a total score ranging from 0 to 30. Higher scores indicate better functional gait and dynamic balance.
Change in Short Physical Performance Battery (SPPB) ScoreBaseline, Week 4, Week 8, and 1-month follow-upLower-limb physical performance was assessed using the Short Physical Performance Battery (SPPB), which includes standing balance, usual gait speed, and repeated chair-stand tests. Each component is scored from 0 to 4, giving a total score ranging from 0 to 12. Higher scores indicate better lower-limb physical performance.
Change in Fugl-Meyer Assessment-Lower Extremity (FMA-LE) Domain ScoresBaseline, Week 4, Week 8, and 1-month follow-upLower-limb sensorimotor function was assessed using the Fugl-Meyer Assessment-Lower Extremity (FMA-LE). The following domains were analyzed separately: lower-extremity motor function (E-F; score range: 0-34), sensation (H; score range: 0-12), passive joint motion (I; score range: 0-20), and joint pain (J; score range: 0-20). Higher scores indicate better motor and sensory function, greater passive joint mobility, and less joint pain, respectively.
Change in Fatigue Severity Scale (FSS) ScoreBaseline, Week 4, Week 8, and 1-month follow-upFatigue was assessed using the Fatigue Severity Scale (FSS), a 9-item questionnaire evaluating the severity and impact of fatigue on daily functioning. Each item is rated from 1 to 7, with higher scores indicating greater fatigue severity.
Intrinsic Motivation Inventory (IMI) Scores2nd, 5th and 8th weekExercise-related motivation was assessed using the 22-item version of the Intrinsic Motivation Inventory (IMI), comprising four subscales: interest/enjoyment, perceived competence, perceived choice, and pressure/tension. Items are rated on a 7-point scale from 1 (not at all true) to 7 (very true), with negatively worded items reverse-scored. Subscale scores are calculated by averaging the corresponding item scores and therefore range from 1 to 7. Higher scores indicate greater levels of the construct represented by each subscale (i.e., greater interest/enjoyment, perceived competence, perceived choice, or pressure/tension). The IMI was administered only to participants in the two intervention groups.

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026