Skip to content

Sensorimotor Integration Exercises on Post-stroke Balance and Fall Efficacy

Effects of Sensorimotor Integration Exercises on Balance and Fall Efficacy in Sub-acute Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03584035
Acronym
SMIE
Enrollment
46
Registered
2018-07-12
Start date
2018-05-02
Completion date
2019-07-30
Last updated
2019-08-13

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

Conditions

Stroke

Keywords

sensory motor integration exercise

Brief summary

To study the effect of sensorimotor integration exercises on balance and fall efficacy in sub-acute stroke by performing 18 balance training exercises with three progressive steps.

Detailed description

Balance impairment after stroke is significantly correlated with fall risk. To improve balance and reduce fall efficacy, the participants in the study group will be trained by six weeks three progressive steps of sensorimotor integration exercises. Each exercise step will take 30 minutes of a practice session, three sessions per week. Conventional physiotherapy (passive and active exercises and lower extremities strengthening exercises) will be given to the control group. The changes in balance performance and fall efficacy will be measured and compared within and between groups.

Interventions

BEHAVIORALsensory motor integration exercises

Sensorimotor integration exercises will be given in study group. The exercises will be performed in standing, sitting and walking. Exercises will be progressively increased from eye open to closed , floor to mat and head turns to right & left under the supervision of physiotherapist. Sensorimotor integration exercises will take 45 minutes in each session.

BEHAVIORALconventional physiotherapy

Conventional physiotherapy will take 30 minutes in each session, taking three sessions per weeks for six weeks. The exercises include simple lower extremity exercise and ambulatory training such as sit to stand, stepping, lateral and backward walking, and tandom walking etc.

Sponsors

University of Medical Technology, Yangon
CollaboratorOTHER
Mahidol University
Lead SponsorOTHER

Study design

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

Masking description

The outcome assessor will do all assessments (pre and post intervention) without group allocation.

Intervention model description

Randomized Control Trial

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* First episode of sub-acute stroke (from 1 to 26 weeks) referred from physicians * Both sexes * Age above 20 * Good cognition (Mini Mental State Examination Scale ≥24) * Moderate and moderately severe disability (Modified Rankin Scale- 3 and 4) * Impaired balance (BBS \<41)

Exclusion criteria

* Recurrent stroke * Associated with other neurological conditions (such as Parkinson's disease, Epilepsy, meningitis) * Deficits of somatic sensation involving the paretic limb (Fugl-Meyer Assessment - sesation\< 1) * Lower extremity weight bearing pain (Fugl-Meyer Assessment- pain \<1) * Low back pain (VAS ≥ 3) * Severe visual deficits which cannot be corrected by lens or glasses * Symptomatic vestibular disorders (Paroxysmal postural vertigo) * Associated serious cardiac disorder

Design outcomes

Primary

MeasureTime frameDescription
Berg Balance Scale (BBS)6 weeks14 items to measure static and dynamic balance

Secondary

MeasureTime frameDescription
Functional Reach Test6 weeksTo assess the stability by measuring the maximum distance while standing in a fixed position
Fall Efficacy Scale6 weeksShort, easy questionnaire that provides information about how much fear of fall, which is comprised of 16-items concerning confidence in maintaing balance during activities.

Countries

Burma

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026