Sensorimotor Integration Exercises on Post-stroke Balance and Fall Efficacy

NCT03584035 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2019-08-13

No results posted yet for this study

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.

Conditions

Interventions

BEHAVIORAL

sensory 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.

BEHAVIORAL

conventional 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 & Collaborators

  • University of Medical Technology, Yangon

    collaborator OTHER
  • Mahidol University

    lead OTHER

Principal Investigators

  • May Phyu Phyu Maung, B.Med.Tech · University of Medical Technology, Yangon

  • Thin Thin Moe, Ph.D · Mahidol University

  • Myo Thuzar Khin, Ph.D · University of Medical Technology, Yangon

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-02
Primary Completion
2019-05-30
Completion
2019-07-30

Countries

  • Burma

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03584035 on ClinicalTrials.gov